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Horizontal gene transfer

From Wikipedia, in a visual modern way
Tree of life showing vertical and horizontal gene transfers
Tree of life showing vertical and horizontal gene transfers

Horizontal gene transfer (HGT) or lateral gene transfer (LGT)[1][2][3] is the movement of genetic material between unicellular and/or multicellular organisms other than by the ("vertical") transmission of DNA from parent to offspring (reproduction).[4] HGT is an important factor in the evolution of many organisms.[5][6] HGT is influencing scientific understanding of higher order evolution while more significantly shifting perspectives on bacterial evolution.[7]

Horizontal gene transfer is the primary mechanism for the spread of antibiotic resistance in bacteria,[8][5][9][10] and plays an important role in the evolution of bacteria that can degrade novel compounds such as human-created pesticides[11] and in the evolution, maintenance, and transmission of virulence.[12] It often involves temperate bacteriophages and plasmids.[13][14][15] Genes responsible for antibiotic resistance in one species of bacteria can be transferred to another species of bacteria through various mechanisms of HGT such as transformation, transduction and conjugation, subsequently arming the antibiotic resistant genes' recipient against antibiotics. The rapid spread of antibiotic resistance genes in this manner is becoming a challenge to manage in the field of medicine. Ecological factors may also play a role in the HGT of antibiotic resistant genes.[16]

Horizontal gene transfer is recognized as a pervasive evolutionary process that distributes genes between divergent prokaryotic lineages[17] and can also involve eukaryotes.[18][19] It is postulated that HGT promotes the maintenance of a universal life biochemistry and, subsequently, the universality of the genetic code.[20]

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Unicellular organism

Unicellular organism

A unicellular organism, also known as a single-celled organism, is an organism that consists of a single cell, unlike a multicellular organism that consists of multiple cells. Organisms fall into two general categories: prokaryotic organisms and eukaryotic organisms. Most prokaryotes are unicellular and are classified into bacteria and archaea. Many eukaryotes are multicellular, but some are unicellular such as protozoa, unicellular algae, and unicellular fungi. Unicellular organisms are thought to be the oldest form of life, with early protocells possibly emerging 3.8–4.0 billion years ago.

Multicellular organism

Multicellular organism

A multicellular organism is an organism that consists of more than one cell, in contrast to unicellular organism.

DNA

DNA

Deoxyribonucleic acid is a polymer composed of two polynucleotide chains that coil around each other to form a double helix. The polymer carries genetic instructions for the development, functioning, growth and reproduction of all known organisms and many viruses. DNA and ribonucleic acid (RNA) are nucleic acids. Alongside proteins, lipids and complex carbohydrates (polysaccharides), nucleic acids are one of the four major types of macromolecules that are essential for all known forms of life.

Reproduction

Reproduction

Reproduction is the biological process by which new individual organisms – "offspring" – are produced from their "parent" or parents. Reproduction is a fundamental feature of all known life; each individual organism exists as the result of reproduction. There are two forms of reproduction: asexual and sexual.

Bacteria

Bacteria

Bacteria are ubiquitous, mostly free-living organisms often consisting of one biological cell. They constitute a large domain of prokaryotic microorganisms. Typically a few micrometres in length, bacteria were among the first life forms to appear on Earth, and are present in most of its habitats. Bacteria inhabit soil, water, acidic hot springs, radioactive waste, and the deep biosphere of Earth's crust. Bacteria are vital in many stages of the nutrient cycle by recycling nutrients such as the fixation of nitrogen from the atmosphere. The nutrient cycle includes the decomposition of dead bodies; bacteria are responsible for the putrefaction stage in this process. In the biological communities surrounding hydrothermal vents and cold seeps, extremophile bacteria provide the nutrients needed to sustain life by converting dissolved compounds, such as hydrogen sulphide and methane, to energy. Bacteria also live in symbiotic and parasitic relationships with plants and animals. Most bacteria have not been characterised and there are many species that cannot be grown in the laboratory. The study of bacteria is known as bacteriology, a branch of microbiology.

Bactericide

Bactericide

A bactericide or bacteriocide, sometimes abbreviated Bcidal, is a substance which kills bacteria. Bactericides are disinfectants, antiseptics, or antibiotics. However, material surfaces can also have bactericidal properties based solely on their physical surface structure, as for example biomaterials like insect wings.

Virulence

Virulence

Virulence is a pathogen's or microorganism's ability to cause damage to a host.

Temperateness (virology)

Temperateness (virology)

In virology, temperate refers to the ability of some bacteriophages to display a lysogenic life cycle. Many temperate phages can integrate their genomes into their host bacterium's chromosome, together becoming a lysogen as the phage genome becomes a prophage. A temperate phage is also able to undergo a productive, typically lytic life cycle, where the prophage is expressed, replicates the phage genome, and produces phage progeny, which then leave the bacterium. With phage the term virulent is often used as an antonym to temperate, but more strictly a virulent phage is one that has lost its ability to display lysogeny through mutation rather than a phage lineage with no genetic potential to ever display lysogeny.

Bacteriophage

Bacteriophage

A bacteriophage, also known informally as a phage, is a duplodnaviria virus that infects and replicates within bacteria and archaea. The term was derived from "bacteria" and the Greek φαγεῖν, meaning "to devour". Bacteriophages are composed of proteins that encapsulate a DNA or RNA genome, and may have structures that are either simple or elaborate. Their genomes may encode as few as four genes and as many as hundreds of genes. Phages replicate within the bacterium following the injection of their genome into its cytoplasm.

Transformation (genetics)

Transformation (genetics)

In molecular biology and genetics, transformation is the genetic alteration of a cell resulting from the direct uptake and incorporation of exogenous genetic material from its surroundings through the cell membrane(s). For transformation to take place, the recipient bacterium must be in a state of competence, which might occur in nature as a time-limited response to environmental conditions such as starvation and cell density, and may also be induced in a laboratory.

Transduction (genetics)

Transduction (genetics)

Transduction is the process by which foreign DNA is introduced into a cell by a virus or viral vector. An example is the viral transfer of DNA from one bacterium to another and hence an example of horizontal gene transfer. Transduction does not require physical contact between the cell donating the DNA and the cell receiving the DNA, and it is DNase resistant. Transduction is a common tool used by molecular biologists to stably introduce a foreign gene into a host cell's genome.

Bacterial conjugation

Bacterial conjugation

Bacterial conjugation is the transfer of genetic material between bacterial cells by direct cell-to-cell contact or by a bridge-like connection between two cells. This takes place through a pilus. It is a parasexual mode of reproduction in bacteria.

History

Griffith's experiment, reported in 1928 by Frederick Griffith,[21] was the first experiment suggesting that bacteria are capable of transferring genetic information through a process known as transformation.[22][23] Griffith's findings were followed by research in the late 1930s and early 40s that isolated DNA as the material that communicated this genetic information.

Horizontal genetic transfer was then described in Seattle in 1951, in a paper demonstrating that the transfer of a viral gene into Corynebacterium diphtheriae created a virulent strain from a non-virulent strain,[24] also simultaneously solving the riddle of diphtheria (that patients could be infected with the bacteria but not have any symptoms, and then suddenly convert later or never),[25] and giving the first example for the relevance of the lysogenic cycle.[26] Inter-bacterial gene transfer was first described in Japan in a 1959 publication that demonstrated the transfer of antibiotic resistance between different species of bacteria.[27][28] In the mid-1980s, Syvanen[29] postulated that biologically significant lateral gene transfer has existed since the beginning of life on Earth and has been involved in shaping all of evolutionary history.

As Jian, Rivera and Lake (1999) put it: "Increasingly, studies of genes and genomes are indicating that considerable horizontal transfer has occurred between prokaryotes"[30] (see also Lake and Rivera, 2007).[31] The phenomenon appears to have had some significance for unicellular eukaryotes as well. As Bapteste et al. (2005) observe, "additional evidence suggests that gene transfer might also be an important evolutionary mechanism in protist evolution."[32]

Grafting of one plant to another can transfer chloroplasts (organelles in plant cells that conduct photosynthesis), mitochondrial DNA, and the entire cell nucleus containing the genome to potentially make a new species.[33] Some Lepidoptera (e.g. monarch butterflies and silkworms) have been genetically modified by horizontal gene transfer from the wasp bracovirus.[34] Bites from insects in the family Reduviidae (assassin bugs) can, via a parasite, infect humans with the trypanosomal Chagas disease, which can insert its DNA into the human genome.[35] It has been suggested that lateral gene transfer to humans from bacteria may play a role in cancer.[36]

Aaron Richardson and Jeffrey D. Palmer state: "Horizontal gene transfer (HGT) has played a major role in bacterial evolution and is fairly common in certain unicellular eukaryotes. However, the prevalence and importance of HGT in the evolution of multicellular eukaryotes remain unclear."[37]

Due to the increasing amount of evidence suggesting the importance of these phenomena for evolution (see below) molecular biologists such as Peter Gogarten have described horizontal gene transfer as "A New Paradigm for Biology".[38]

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Griffith's experiment

Griffith's experiment

Griffith's experiment, reported in 1928 by Frederick Griffith, was the first experiment suggesting that bacteria are capable of transferring genetic information through a process known as transformation. Griffith's findings were followed by research in the late 1930s and early 40s that isolated DNA as the material that communicated this genetic information.

Frederick Griffith

Frederick Griffith

Frederick Griffith (1877–1941) was a British bacteriologist whose focus was the epidemiology and pathology of bacterial pneumonia. In January 1928 he reported what is now known as Griffith's Experiment, the first widely accepted demonstrations of bacterial transformation, whereby a bacterium distinctly changes its form and function.

Avery–MacLeod–McCarty experiment

Avery–MacLeod–McCarty experiment

The Avery–MacLeod–McCarty experiment was an experimental demonstration, reported in 1944 by Oswald Avery, Colin MacLeod, and Maclyn McCarty, that DNA is the substance that causes bacterial transformation, in an era when it had been widely believed that it was proteins that served the function of carrying genetic information. It was the culmination of research in the 1930s and early 20th century at the Rockefeller Institute for Medical Research to purify and characterize the "transforming principle" responsible for the transformation phenomenon first described in Griffith's experiment of 1928: killed Streptococcus pneumoniae of the virulent strain type III-S, when injected along with living but non-virulent type II-R pneumococci, resulted in a deadly infection of type III-S pneumococci. In their paper "Studies on the Chemical Nature of the Substance Inducing Transformation of Pneumococcal Types: Induction of Transformation by a Desoxyribonucleic Acid Fraction Isolated from Pneumococcus Type III", published in the February 1944 issue of the Journal of Experimental Medicine, Avery and his colleagues suggest that DNA, rather than protein as widely believed at the time, may be the hereditary material of bacteria, and could be analogous to genes and/or viruses in higher organisms.

DNA

DNA

Deoxyribonucleic acid is a polymer composed of two polynucleotide chains that coil around each other to form a double helix. The polymer carries genetic instructions for the development, functioning, growth and reproduction of all known organisms and many viruses. DNA and ribonucleic acid (RNA) are nucleic acids. Alongside proteins, lipids and complex carbohydrates (polysaccharides), nucleic acids are one of the four major types of macromolecules that are essential for all known forms of life.

Corynebacterium diphtheriae

Corynebacterium diphtheriae

Corynebacterium diphtheriae is the pathogenic bacterium that causes diphtheria. It is also known as the Klebs–Löffler bacillus, because it was discovered in 1884 by German bacteriologists Edwin Klebs (1834–1912) and Friedrich Löffler (1852–1915). The bacteria are usually harmless unless they are infected by a bacteriophage that carries a gene that gives rise to a toxin. This toxin causes the disease. Diphtheria is caused by the adhesion and infiltration of the bacteria into the mucosal layers of the body, primarily affecting the respiratory tract and the subsequent release of an endotoxin. The toxin has a localized effect on skin lesions, as well as a metastatic, proteolytic effects on other organ systems in severe infections. Originally a major cause of childhood mortality, diphtheria has been almost entirely eradicated due to the vigorous administration of the diphtheria vaccination in the 1910s.

Diphtheria

Diphtheria

Diphtheria is an infection caused by the bacterium Corynebacterium diphtheriae. Most infections are asymptomatic or have a mild clinical course, but in some outbreaks more than 10% of those diagnosed with the disease may die. Signs and symptoms may vary from mild to severe and usually start two to five days after exposure. Symptoms often come on fairly gradually, beginning with a sore throat and fever. In severe cases, a grey or white patch develops in the throat. This can block the airway and create a barking cough as in croup. The neck may swell in part due to enlarged lymph nodes. A form of diphtheria which involves the skin, eyes or genitals also exists. Complications may include myocarditis, inflammation of nerves, kidney problems, and bleeding problems due to low levels of platelets. Myocarditis may result in an abnormal heart rate and inflammation of the nerves may result in paralysis.

Bacteria

Bacteria

Bacteria are ubiquitous, mostly free-living organisms often consisting of one biological cell. They constitute a large domain of prokaryotic microorganisms. Typically a few micrometres in length, bacteria were among the first life forms to appear on Earth, and are present in most of its habitats. Bacteria inhabit soil, water, acidic hot springs, radioactive waste, and the deep biosphere of Earth's crust. Bacteria are vital in many stages of the nutrient cycle by recycling nutrients such as the fixation of nitrogen from the atmosphere. The nutrient cycle includes the decomposition of dead bodies; bacteria are responsible for the putrefaction stage in this process. In the biological communities surrounding hydrothermal vents and cold seeps, extremophile bacteria provide the nutrients needed to sustain life by converting dissolved compounds, such as hydrogen sulphide and methane, to energy. Bacteria also live in symbiotic and parasitic relationships with plants and animals. Most bacteria have not been characterised and there are many species that cannot be grown in the laboratory. The study of bacteria is known as bacteriology, a branch of microbiology.

Eukaryote

Eukaryote

Eukaryota, whose members are known as eukaryotes, is a diverse domain of organisms whose cells have a nucleus. All animals, plants, fungi, and many unicellular organisms, are eukaryotes. They belong to the group of organisms Eukaryota or Eukarya, which is one of the three domains of life. Bacteria and Archaea make up the other two domains.

Chloroplast

Chloroplast

A chloroplast is a type of membrane-bound organelle known as a plastid that conducts photosynthesis mostly in plant and algal cells. The photosynthetic pigment chlorophyll captures the energy from sunlight, converts it, and stores it in the energy-storage molecules ATP and NADPH while freeing oxygen from water in the cells. The ATP and NADPH is then used to make organic molecules from carbon dioxide in a process known as the Calvin cycle. Chloroplasts carry out a number of other functions, including fatty acid synthesis, amino acid synthesis, and the immune response in plants. The number of chloroplasts per cell varies from one, in unicellular algae, up to 100 in plants like Arabidopsis and wheat.

Cell nucleus

Cell nucleus

The cell nucleus is a membrane-bound organelle found in eukaryotic cells. Eukaryotic cells usually have a single nucleus, but a few cell types, such as mammalian red blood cells, have no nuclei, and a few others including osteoclasts have many. The main structures making up the nucleus are the nuclear envelope, a double membrane that encloses the entire organelle and isolates its contents from the cellular cytoplasm; and the nuclear matrix, a network within the nucleus that adds mechanical support.

Genome

Genome

In the fields of molecular biology and genetics, a genome is all the genetic information of an organism. It consists of nucleotide sequences of DNA. The nuclear genome includes protein-coding genes and non-coding genes, other functional regions of the genome such as regulatory sequences, and often a substantial fraction of 'junk' DNA with no evident function. Almost all eukaryotes have mitochondria and a small mitochondrial genome. Algae and plants also contain chloroplasts with a chloroplast genome.

Lepidoptera

Lepidoptera

Lepidoptera is an order of insects that includes butterflies and moths. About 180,000 species of the Lepidoptera are described, in 126 families and 46 superfamilies, 10 percent of the total described species of living organisms. It is one of the most widespread and widely recognizable insect orders in the world. The Lepidoptera show many variations of the basic body structure that have evolved to gain advantages in lifestyle and distribution. Recent estimates suggest the order may have more species than earlier thought, and is among the four most species-rich orders, along with the Hymenoptera, Diptera, and Coleoptera.

Mechanisms

There are several mechanisms for horizontal gene transfer:[5][39][40]

Horizontal transposon transfer

A transposable element (TE) (also called a transposon or jumping gene) is a mobile segment of DNA that can sometimes pick up a resistance gene and insert it into a plasmid or chromosome, thereby inducing horizontal gene transfer of antibiotic resistance.[41]

Horizontal transposon transfer (HTT) refers to the passage of pieces of DNA that are characterized by their ability to move from one locus to another between genomes by means other than parent-to-offspring inheritance. Horizontal gene transfer has long been thought to be crucial to prokaryotic evolution, but there is a growing amount of data showing that HTT is a common and widespread phenomenon in eukaryote evolution as well.[44] On the transposable element side, spreading between genomes via horizontal transfer may be viewed as a strategy to escape purging due to purifying selection, mutational decay and/or host defense mechanisms.[45]

HTT can occur with any type of transposable elements, but DNA transposons and LTR retroelements are more likely to be capable of HTT because both have a stable, double-stranded DNA intermediate that is thought to be sturdier than the single-stranded RNA intermediate of non-LTR retroelements, which can be highly degradable.[44] Non-autonomous elements may be less likely to transfer horizontally compared to autonomous elements because they do not encode the proteins required for their own mobilization. The structure of these non-autonomous elements generally consists of an intronless gene encoding a transposase protein, and may or may not have a promoter sequence. Those that do not have promoter sequences encoded within the mobile region rely on adjacent host promoters for expression.[44] Horizontal transfer is thought to play an important role in the TE life cycle.[44]

HTT has been shown to occur between species and across continents in both plants[46] and animals (Ivancevic et al. 2013), though some TEs have been shown to more successfully colonize the genomes of certain species over others.[47] Both spatial and taxonomic proximity of species has been proposed to favor HTTs in plants and animals.[46] It is unknown how the density of a population may affect the rate of HTT events within a population, but close proximity due to parasitism and cross contamination due to crowding have been proposed to favor HTT in both plants and animals.[46] Successful transfer of a transposable element requires delivery of DNA from donor to host cell (and to the germ line for multi-cellular organisms), followed by integration into the recipient host genome.[44] Though the actual mechanism for the transportation of TEs from donor cells to host cells is unknown, it is established that naked DNA and RNA can circulate in bodily fluid.[44] Many proposed vectors include arthropods, viruses, freshwater snails (Ivancevic et al. 2013), endosymbiotic bacteria,[45] and intracellular parasitic bacteria.[44] In some cases, even TEs facilitate transport for other TEs.[47]

The arrival of a new TE in a host genome can have detrimental consequences because TE mobility may induce mutation. However, HTT can also be beneficial by introducing new genetic material into a genome and promoting the shuffling of genes and TE domains among hosts, which can be co-opted by the host genome to perform new functions.[47] Moreover, transposition activity increases the TE copy number and generates chromosomal rearrangement hotspots.[48] HTT detection is a difficult task because it is an ongoing phenomenon that is constantly changing in frequency of occurrence and composition of TEs inside host genomes. Furthermore, few species have been analyzed for HTT, making it difficult to establish patterns of HTT events between species. These issues can lead to the underestimation or overestimation of HTT events between ancestral and current eukaryotic species.[48]

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Cell (biology)

Cell (biology)

The cell is the basic structural and functional unit of life forms. Every cell consists of a cytoplasm enclosed within a membrane, and contains many biomolecules such as proteins, DNA and RNA, as well as many small molecules of nutrients and metabolites. The term comes from the Latin word cellula meaning 'small room'.

Gene expression

Gene expression

Gene expression is the process by which information from a gene is used in the synthesis of a functional gene product that enables it to produce end products, protein or non-coding RNA, and ultimately affect a phenotype, as the final effect. These products are often proteins, but in non-protein-coding genes such as transfer RNA (tRNA) and small nuclear RNA (snRNA), the product is a functional non-coding RNA. Gene expression is summarized in the central dogma of molecular biology first formulated by Francis Crick in 1958, further developed in his 1970 article, and expanded by the subsequent discoveries of reverse transcription and RNA replication.

DNA

DNA

Deoxyribonucleic acid is a polymer composed of two polynucleotide chains that coil around each other to form a double helix. The polymer carries genetic instructions for the development, functioning, growth and reproduction of all known organisms and many viruses. DNA and ribonucleic acid (RNA) are nucleic acids. Alongside proteins, lipids and complex carbohydrates (polysaccharides), nucleic acids are one of the four major types of macromolecules that are essential for all known forms of life.

RNA

RNA

Ribonucleic acid (RNA) is a polymeric molecule essential in various biological roles in coding, decoding, regulation and expression of genes. RNA and deoxyribonucleic acid (DNA) are nucleic acids. Along with lipids, proteins, and carbohydrates, nucleic acids constitute one of the four major macromolecules essential for all known forms of life. Like DNA, RNA is assembled as a chain of nucleotides, but unlike DNA, RNA is found in nature as a single strand folded onto itself, rather than a paired double strand. Cellular organisms use messenger RNA (mRNA) to convey genetic information that directs synthesis of specific proteins. Many viruses encode their genetic information using an RNA genome.

Molecular biology

Molecular biology

Molecular biology is the branch of biology that seeks to understand the molecular basis of biological activity in and between cells, including biomolecular synthesis, modification, mechanisms, and interactions. The study of chemical and physical structure of biological macromolecules is known as molecular biology.

Biotechnology

Biotechnology

Biotechnology is the integration of natural sciences and engineering sciences in order to achieve the application of organisms, cells, parts thereof and molecular analogues for products and services. The term biotechnology was first used by Károly Ereky in 1919, meaning the production of products from raw materials with the aid of living organisms.

Bacterial conjugation

Bacterial conjugation

Bacterial conjugation is the transfer of genetic material between bacterial cells by direct cell-to-cell contact or by a bridge-like connection between two cells. This takes place through a pilus. It is a parasexual mode of reproduction in bacteria.

Gene transfer agent

Gene transfer agent

Gene transfer agents (GTAs) are DNA-containing virus-like particles that are produced by some bacteria and archaea and mediate horizontal gene transfer. Different GTA types have originated independently from viruses in several bacterial and archaeal lineages. These cells produce GTA particles containing short segments of the DNA present in the cell. After the particles are released from the producer cell, they can attach to related cells and inject their DNA into the cytoplasm. The DNA can then become part of the recipient cells' genome.

Alphaproteobacteria

Alphaproteobacteria

Alphaproteobacteria is a class of bacteria in the phylum Pseudomonadota. The Magnetococcales and Mariprofundales are considered basal or sister to the Alphaproteobacteria. The Alphaproteobacteria are highly diverse and possess few commonalities, but nevertheless share a common ancestor. Like all Proteobacteria, its members are gram-negative and some of its intracellular parasitic members lack peptidoglycan and are consequently gram variable.

Rhodobacterales

Rhodobacterales

Rhodobacterales are an order of the Alphaproteobacteria.

Eukaryote

Eukaryote

Eukaryota, whose members are known as eukaryotes, is a diverse domain of organisms whose cells have a nucleus. All animals, plants, fungi, and many unicellular organisms, are eukaryotes. They belong to the group of organisms Eukaryota or Eukarya, which is one of the three domains of life. Bacteria and Archaea make up the other two domains.

DNA transposon

DNA transposon

DNA transposons are DNA sequences, sometimes referred to "jumping genes", that can move and integrate to different locations within the genome. They are class II transposable elements (TEs) that move through a DNA intermediate, as opposed to class I TEs, retrotransposons, that move through an RNA intermediate. DNA transposons can move in the DNA of an organism via a single-or double-stranded DNA intermediate. DNA transposons have been found in both prokaryotic and eukaryotic organisms. They can make up a significant portion of an organism's genome, particularly in eukaryotes. In prokaryotes, TE's can facilitate the horizontal transfer of antibiotic resistance or other genes associated with virulence. After replicating and propagating in a host, all transposon copies become inactivated and are lost unless the transposon passes to a genome by starting a new life cycle with horizontal transfer. It is important to note that DNA transposons do not randomly insert themselves into the genome, but rather show preference for specific sites.

Methods of detection

A speciation event produces orthologs of a gene in the two daughter species. A horizontal gene transfer event from one species to another adds a xenolog of the gene to the receiving genome.
A speciation event produces orthologs of a gene in the two daughter species. A horizontal gene transfer event from one species to another adds a xenolog of the gene to the receiving genome.

Horizontal gene transfer is typically inferred using bioinformatics methods, either by identifying atypical sequence signatures ("parametric" methods) or by identifying strong discrepancies between the evolutionary history of particular sequences compared to that of their hosts. The transferred gene (xenolog) found in the receiving species is more closely related to the genes of the donor species than would be expected.

Viruses

The virus called Mimivirus infects amoebae. Another virus, called Sputnik, also infects amoebae, but it cannot reproduce unless mimivirus has already infected the same cell.[49] "Sputnik's genome reveals further insight into its biology. Although 13 of its genes show little similarity to any other known genes, three are closely related to mimivirus and mamavirus genes, perhaps cannibalized by the tiny virus as it packaged up particles sometime in its history. This suggests that the satellite virus could perform horizontal gene transfer between viruses, paralleling the way that bacteriophages ferry genes between bacteria."[50] Horizontal transfer is also seen between geminiviruses and tobacco plants.[51]

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Virus

Virus

A virus is a submicroscopic infectious agent that replicates only inside the living cells of an organism. Viruses infect all life forms, from animals and plants to microorganisms, including bacteria and archaea. Since Dmitri Ivanovsky's 1892 article describing a non-bacterial pathogen infecting tobacco plants and the discovery of the tobacco mosaic virus by Martinus Beijerinck in 1898, more than 9,000 of the millions of virus species have been described in detail. Viruses are found in almost every ecosystem on Earth and are the most numerous type of biological entity. The study of viruses is known as virology, a subspeciality of microbiology.

Mimivirus

Mimivirus

Mimivirus is a genus of giant viruses, in the family Mimiviridae. Amoeba serve as their natural hosts. This genus contains a single identified species named Acanthamoeba polyphaga mimivirus (APMV). It also refers to a group of phylogenetically related large viruses.

Genome

Genome

In the fields of molecular biology and genetics, a genome is all the genetic information of an organism. It consists of nucleotide sequences of DNA. The nuclear genome includes protein-coding genes and non-coding genes, other functional regions of the genome such as regulatory sequences, and often a substantial fraction of 'junk' DNA with no evident function. Almost all eukaryotes have mitochondria and a small mitochondrial genome. Algae and plants also contain chloroplasts with a chloroplast genome.

Mamavirus

Mamavirus

Mamavirus is a large and complex virus in the Group I family Mimiviridae. The virus is exceptionally large, and larger than many bacteria. Mamavirus and other mimiviridae belong to nucleocytoplasmic large DNA virus (NCLDVs) family. Mamavirus can be compared to the similar complex virus mimivirus; mamavirus was so named because it is similar to but larger than mimivirus.

Prokaryotes

Horizontal gene transfer is common among bacteria, even among very distantly related ones. This process is thought to be a significant cause of increased drug resistance[5][52] when one bacterial cell acquires resistance, and the resistance genes are transferred to other species.[53][54] Transposition and horizontal gene transfer, along with strong natural selective forces have led to multi-drug resistant strains of S. aureus and many other pathogenic bacteria.[41] Horizontal gene transfer also plays a role in the spread of virulence factors, such as exotoxins and exoenzymes, amongst bacteria.[5] A prime example concerning the spread of exotoxins is the adaptive evolution of Shiga toxins in E. coli through horizontal gene transfer via transduction with Shigella species of bacteria.[55] Strategies to combat certain bacterial infections by targeting these specific virulence factors and mobile genetic elements have been proposed.[12] For example, horizontally transferred genetic elements play important roles in the virulence of E. coli, Salmonella, Streptococcus and Clostridium perfringens.[5]

In prokaryotes, restriction-modification systems are known to provide immunity against horizontal gene transfer and in stabilizing mobile genetic elements. Genes encoding restriction modification systems have been reported to move between prokaryotic genomes within mobile genetic elements (MGE) such as plasmids, prophages, insertion sequences/transposons, integrative conjugative elements (ICE),[56] and integrons. Still, they are more frequently a chromosomal-encoded barrier to MGE than an MGE-encoded tool for cell infection.[57]

Lateral gene transfer via a mobile genetic element, namely the integrated conjugative element (ICE) Bs1 has been reported for its role in the global DNA damage SOS response of the gram positive Bacillus subtilis.[58] Furthermore, it has been linked with the radiation and desiccation resistance of Bacillus pumilus SAFR-032 spores,[59] isolated from spacecraft cleanroom facilities.[60][61][62]

Transposon insertion elements have been reported to increase the fitness of gram-negative E. coli strains through either major transpositions or genome rearrangements, and increasing mutation rates.[63][64] In a study on the effects of long-term exposure of simulated microgravity on non-pathogenic E. coli, the results showed transposon insertions occur at loci, linked to SOS stress response.[65] When the same E. coli strain was exposed to a combination of simulated microgravity and trace (background) levels of (the broad spectrum) antibiotic (chloramphenicol), the results showed transposon-mediated rearrangements (TMRs), disrupting genes involved in bacterial adhesion, and deleting an entire segment of several genes involved with motility and chemotaxis.[66] Both these studies have implications for microbial growth, adaptation to and antibiotic resistance in real time space conditions.

Horizontal gene transfer is particularly active in bacterial genomes around the production of secondary or specialized metabolites.[67] This is clearly exhibited within certain groups of bacteria including P. aeruginosa and actinomycetales, an order of Actinomycetota. Polyketide synthases (PKSs) and biosynthetic gene clusters provide modular organizations of associated genes making these bacteria well-adapted to acquire and discard helpful modular modifications via HGT. Certain areas of genes known as hotspots further increase the likelihood of horizontally transferred secondary metabolite-producing genes.[68] The promiscuity of enzymes is a reoccurring theme in this particular theatre.

Bacterial transformation

1: Donor bacteria   2: Bacteria who will receive the gene   3: The red portion represents the gene that will be transferred.   Transformation in bacteria happens in a certain environment.
1: Donor bacteria 2: Bacteria who will receive the gene 3: The red portion represents the gene that will be transferred. Transformation in bacteria happens in a certain environment.

Natural transformation is a bacterial adaptation for DNA transfer (HGT) that depends on the expression of numerous bacterial genes whose products are responsible for this process.[69][70] In general, transformation is a complex, energy-requiring developmental process. In order for a bacterium to bind, take up and recombine exogenous DNA into its chromosome, it must become competent, that is, enter a special physiological state. Competence development in Bacillus subtilis requires expression of about 40 genes.[71] The DNA integrated into the host chromosome is usually (but with infrequent exceptions) derived from another bacterium of the same species, and is thus homologous to the resident chromosome. The capacity for natural transformation occurs in at least 67 prokaryotic species.[70] Competence for transformation is typically induced by high cell density and/or nutritional limitation, conditions associated with the stationary phase of bacterial growth. Competence appears to be an adaptation for DNA repair.[72] Transformation in bacteria can be viewed as a primitive sexual process, since it involves interaction of homologous DNA from two individuals to form recombinant DNA that is passed on to succeeding generations. Although transduction is the form of HGT most commonly associated with bacteriophages, certain phages may also be able to promote transformation.[73]

Bacterial conjugation

1: Donor bacteria cell (F+ cell)   2: Bacteria that receives the plasmid (F- cell)   3: Plasmid that will be moved to the other bacteria   4: Pilus.   Conjugation in bacteria using a sex pilus; then the bacteria that received the plasmid can go give it to other bacteria as well.
1: Donor bacteria cell (F+ cell) 2: Bacteria that receives the plasmid (F- cell) 3: Plasmid that will be moved to the other bacteria 4: Pilus. Conjugation in bacteria using a sex pilus; then the bacteria that received the plasmid can go give it to other bacteria as well.

Conjugation in Mycobacterium smegmatis, like conjugation in E. coli, requires stable and extended contact between a donor and a recipient strain, is DNase resistant, and the transferred DNA is incorporated into the recipient chromosome by homologous recombination. However, unlike E. coli high frequency of recombination conjugation (Hfr), mycobacterial conjugation is a type of HGT that is chromosome rather than plasmid based.[74] Furthermore, in contrast to E. coli (Hfr) conjugation, in M. smegmatis all regions of the chromosome are transferred with comparable efficiencies. Substantial blending of the parental genomes was found as a result of conjugation, and this blending was regarded as reminiscent of that seen in the meiotic products of sexual reproduction.[74][75]

Archaeal DNA transfer

The archaeon Sulfolobus solfataricus, when UV irradiated, strongly induces the formation of type IV pili which then facilitates cellular aggregation.[76][77] Exposure to chemical agents that cause DNA damage also induces cellular aggregation.[76] Other physical stressors, such as temperature shift or pH, do not induce aggregation, suggesting that DNA damage is a specific inducer of cellular aggregation.

UV-induced cellular aggregation mediates intercellular chromosomal HGT marker exchange with high frequency,[78] and UV-induced cultures display recombination rates that exceed those of uninduced cultures by as much as three orders of magnitude. S. solfataricus cells aggregate preferentially with other cells of their own species.[78] Frols et al.[76][79] and Ajon et al.[78] suggested that UV-inducible DNA transfer is likely an important mechanism for providing increased repair of damaged DNA via homologous recombination. This process can be regarded as a simple form of sexual interaction.

Another thermophilic species, Sulfolobus acidocaldarius, is able to undergo HGT. S. acidocaldarius can exchange and recombine chromosomal markers at temperatures up to 84 °C.[80] UV exposure induces pili formation and cellular aggregation.[78] Cells with the ability to aggregate have greater survival than mutants lacking pili that are unable to aggregate. The frequency of recombination is increased by DNA damage induced by UV-irradiation[81] and by DNA damaging chemicals.[82]

The ups operon, containing five genes, is highly induced by UV irradiation. The proteins encoded by the ups operon are employed in UV-induced pili assembly and cellular aggregation leading to intercellular DNA exchange and homologous recombination.[83] Since this system increases the fitness of S. acidocaldarius cells after UV exposure, Wolferen et al.[83][84] considered that transfer of DNA likely takes place in order to repair UV-induced DNA damages by homologous recombination.

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Drug resistance

Drug resistance

Drug resistance is the reduction in effectiveness of a medication such as an antimicrobial or an antineoplastic in treating a disease or condition. The term is used in the context of resistance that pathogens or cancers have "acquired", that is, resistance has evolved. Antimicrobial resistance and antineoplastic resistance challenge clinical care and drive research. When an organism is resistant to more than one drug, it is said to be multidrug-resistant.

Exotoxin

Exotoxin

An exotoxin is a toxin secreted by bacteria. An exotoxin can cause damage to the host by destroying cells or disrupting normal cellular metabolism. They are highly potent and can cause major damage to the host. Exotoxins may be secreted, or, similar to endotoxins, may be released during lysis of the cell. Gram negative pathogens may secrete outer membrane vesicles containing lipopolysaccharide endotoxin and some virulence proteins in the bounding membrane along with some other toxins as intra-vesicular contents, thus adding a previously unforeseen dimension to the well-known eukaryote process of membrane vesicle trafficking, which is quite active at the host–pathogen interface.

Exoenzyme

Exoenzyme

An exoenzyme, or extracellular enzyme, is an enzyme that is secreted by a cell and functions outside that cell. Exoenzymes are produced by both prokaryotic and eukaryotic cells and have been shown to be a crucial component of many biological processes. Most often these enzymes are involved in the breakdown of larger macromolecules. The breakdown of these larger macromolecules is critical for allowing their constituents to pass through the cell membrane and enter into the cell. For humans and other complex organisms, this process is best characterized by the digestive system which breaks down solid food via exoenzymes. The small molecules, generated by the exoenzyme activity, enter into cells and are utilized for various cellular functions. Bacteria and fungi also produce exoenzymes to digest nutrients in their environment, and these organisms can be used to conduct laboratory assays to identify the presence and function of such exoenzymes. Some pathogenic species also use exoenzymes as virulence factors to assist in the spread of these disease-causing microorganisms. In addition to the integral roles in biological systems, different classes of microbial exoenzymes have been used by humans since pre-historic times for such diverse purposes as food production, biofuels, textile production and in the paper industry. Another important role that microbial exoenzymes serve is in the natural ecology and bioremediation of terrestrial and marine environments.

Escherichia coli

Escherichia coli

Escherichia coli, also known as E. coli, is a Gram-negative, facultative anaerobic, rod-shaped, coliform bacterium of the genus Escherichia that is commonly found in the lower intestine of warm-blooded organisms. Most E. coli strains are harmless, but some serotypes (EPEC, ETEC etc.) can cause serious food poisoning in their hosts, and are occasionally responsible for food contamination incidents that prompt product recalls. Most strains do not cause disease in humans and are part of the normal microbiota of the gut; such strains are harmless or even beneficial to humans (although these strains tend to be less studied than the pathogenic ones). For example, some strains of E. coli benefit their hosts by producing vitamin K2 or by preventing the colonization of the intestine by pathogenic bacteria. These mutually beneficial relationships between E. coli and humans are a type of mutualistic biological relationship — where both the humans and the E. coli are benefitting each other. E. coli is expelled into the environment within fecal matter. The bacterium grows massively in fresh faecal matter under aerobic conditions for three days, but its numbers decline slowly afterwards.

Clostridium perfringens

Clostridium perfringens

Clostridium perfringens is a Gram-positive, rod-shaped, anaerobic, spore-forming pathogenic bacterium of the genus Clostridium. C. perfringens is ever-present in nature and can be found as a normal component of decaying vegetation, marine sediment, the intestinal tract of humans and other vertebrates, insects, and soil. It has the shortest reported generation time of any organism at 6.3 minutes in thioglycolate medium.

Mobile genetic elements

Mobile genetic elements

Mobile genetic elements (MGEs) sometimes called selfish genetic elements are a type of genetic material that can move around within a genome, or that can be transferred from one species or replicon to another. MGEs are found in all organisms. In humans, approximately 50% of the genome is thought to be MGEs. MGEs play a distinct role in evolution. Gene duplication events can also happen through the mechanism of MGEs. MGEs can also cause mutations in protein coding regions, which alters the protein functions. These mechanisms can also rearrange genes in the host genome generating variation. These mechanism can increase fitness by gaining new or additional functions. An example of MGEs in evolutionary context are that virulence factors and antibiotic resistance genes of MGEs can be transported to share genetic code with neighboring bacteria. However, MGEs can also decrease fitness by introducing disease-causing alleles or mutations. The set of MGEs in an organism is called a mobilome, which is composed of a large number of plasmids, transposons and viruses.

Plasmid

Plasmid

A plasmid is a small, extrachromosomal DNA molecule within a cell that is physically separated from chromosomal DNA and can replicate independently. They are most commonly found as small circular, double-stranded DNA molecules in bacteria; however, plasmids are sometimes present in archaea and eukaryotic organisms. In nature, plasmids often carry genes that benefit the survival of the organism and confer selective advantage such as antibiotic resistance. While chromosomes are large and contain all the essential genetic information for living under normal conditions, plasmids are usually very small and contain only additional genes that may be useful in certain situations or conditions. Artificial plasmids are widely used as vectors in molecular cloning, serving to drive the replication of recombinant DNA sequences within host organisms. In the laboratory, plasmids may be introduced into a cell via transformation. Synthetic plasmids are available for procurement over the internet.

Prophage

Prophage

A prophage is a bacteriophage genome that is integrated into the circular bacterial chromosome or exists as an extrachromosomal plasmid within the bacterial cell. Integration of prophages into the bacterial host is the characteristic step of the lysogenic cycle of temperate phages. Prophages remain latent in the genome through multiple cell divisions until activation by an external factor, such as UV light, leading to production of new phage particles that will lyse the cell and spread. As ubiquitous mobile genetic elements, prophages play important roles in bacterial genetics and evolution, such as in the acquisition of virulence factors.

Integron

Integron

Integrons are genetic mechanisms that allow bacteria to adapt and evolve rapidly through the stockpiling and expression of new genes. These genes are embedded in a specific genetic structure called gene cassette that generally carries one promoterless open reading frame (ORF) together with a recombination site (attC). Integron cassettes are incorporated to the attI site of the integron platform by site-specific recombination reactions mediated by the integrase.

Chloramphenicol

Chloramphenicol

Chloramphenicol is an antibiotic useful for the treatment of a number of bacterial infections. This includes use as an eye ointment to treat conjunctivitis. By mouth or by injection into a vein, it is used to treat meningitis, plague, cholera, and typhoid fever. Its use by mouth or by injection is only recommended when safer antibiotics cannot be used. Monitoring both blood levels of the medication and blood cell levels every two days is recommended during treatment.

Polyketide synthase

Polyketide synthase

Polyketide synthases (PKSs) are a family of multi-domain enzymes or enzyme complexes that produce polyketides, a large class of secondary metabolites, in bacteria, fungi, plants, and a few animal lineages. The biosyntheses of polyketides share striking similarities with fatty acid biosynthesis.

Metabolic gene cluster

Metabolic gene cluster

Metabolic gene clusters or biosynthetic gene clusters are tightly linked sets of mostly non-homologous genes participating in a common, discrete metabolic pathway. The genes are in physical vicinity to each other on the genome, and their expression is often coregulated. Metabolic gene clusters are common features of bacterial and most fungal genomes, and are less often found in other organisms. They are most widely known for producing secondary metabolites, which are the source or basis of most pharmaceutical compounds, natural toxins, and chemical communication and chemical warfare between organisms. Metabolic gene clusters are also involved in nutrient acquisition, toxin degradation, antimicrobial resistance, and vitamin biosynthesis. Given all these properties of metabolic gene clusters, they play a key role in shaping microbial ecosystems, including microbiome-host interactions. Thus several computational genomics tools have been developed to predict metabolic gene clusters.

Eukaryotes

"Sequence comparisons suggest recent horizontal transfer of many genes among diverse species including across the boundaries of phylogenetic 'domains'. Thus determining the phylogenetic history of a species can not be done conclusively by determining evolutionary trees for single genes."[85]

Organelle to nuclear genome

Organelle to organelle

Viruses to plants

  • Plants are capable of receiving genetic information from viruses by horizontal gene transfer.[51]

Bacteria to fungi

Bacteria to plants

  • Agrobacterium, a pathogenic bacterium that causes cells to proliferate as crown galls and proliferating roots is an example of a bacterium that can transfer genes to plants and this plays an important role in plant evolution.[91]

Bacteria to insects

  • HhMAN1 is a gene in the genome of the coffee berry borer (Hypothenemus hampei) that resembles bacterial genes, and is thought to be transferred from bacteria in the beetle's gut.[92][93]
  • oskar is an essential gene for the specification of the germline in Holometabola and its origin is through to be due to a HGT event followed by a fusion with a LOTUS domain.[94]

Bacteria to animals

  • Bdelloid rotifers currently hold the 'record' for HGT in animals with ~8% of their genes from bacterial origins.[95] Tardigrades were thought to break the record with 17.5% HGT, but that finding was an artifact of bacterial contamination.[96]
  • A study found the genomes of 40 animals (including 10 primates, four Caenorhabditis worms, and 12 Drosophila insects) contained genes which the researchers concluded had been transferred from bacteria and fungi by horizontal gene transfer.[97] The researchers estimated that for some nematodes and Drosophila insects these genes had been acquired relatively recently.[98]
  • A bacteriophage-mediated mechanism transfers genes between prokaryotes and eukaryotes.[99] Nuclear localization signals in bacteriophage terminal proteins (TP) prime DNA replication and become covalently linked to the viral genome. The role of virus and bacteriophages in HGT in bacteria, suggests that TP-containing genomes could be a vehicle of inter-kingdom genetic information transference all throughout evolution.[100]

Endosymbiont to insects and nematodes

  • The adzuki bean beetle has acquired genetic material from its (non-beneficial) endosymbiont Wolbachia.[101] New examples have recently been reported demonstrating that Wolbachia bacteria represent an important potential source of genetic material in arthropods and filarial nematodes.[102]
  • The psyllid Pachypsylla venusta has acquired genes from its current endosymbiont Carsonella, and from many of its historical endosymbionts, too.[103]

Plant to plant

Plants to animals

Plant to fungus

  • Gene transfer between plants and fungi has been posited for a number of cases, including rice (Oryza sativa).
  • Evidence of gene transfer from plants was documented in the fungus Colletotrichum.[110]
  • Plant expansin genes were transferred to fungi further enabling the fungi to infect plants.[111]

Plant to bacteria

  • Plant expansin genes were transferred to bacteria further enabling the bacteria to infect plants.[111]

Fungi to insects

Fungi to fungi

  • The toxin α-amanitin is found in numerous, seemingly unrelated genera fungi such as Amanita, Lepiota, and Galerina. Two biosynthetic genes involved in the production of α-amanitin are P450-29 and FMO1. Phylogenetic and genetic analyses of these genes strongly indicate that they were transferred between the genera via horizontal gene transfer.[114]

Animals to animals

Animals to bacteria

  • The strikingly fish-like copper/zinc superoxide dismutase of Photobacterium leiognathi[116] is most easily explained in terms of transfer of a gene from an ancestor of its fish host.

Human to protozoan

Human genome

  • One study identified approximately 100 of humans' approximately 20,000 total genes which likely resulted from horizontal gene transfer,[118] but this number has been challenged by several researchers arguing these candidate genes for HGT are more likely the result of gene loss combined with differences in the rate of evolution.[119]

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Chloroplast

Chloroplast

A chloroplast is a type of membrane-bound organelle known as a plastid that conducts photosynthesis mostly in plant and algal cells. The photosynthetic pigment chlorophyll captures the energy from sunlight, converts it, and stores it in the energy-storage molecules ATP and NADPH while freeing oxygen from water in the cells. The ATP and NADPH is then used to make organic molecules from carbon dioxide in a process known as the Calvin cycle. Chloroplasts carry out a number of other functions, including fatty acid synthesis, amino acid synthesis, and the immune response in plants. The number of chloroplasts per cell varies from one, in unicellular algae, up to 100 in plants like Arabidopsis and wheat.

Endosymbiont

Endosymbiont

An endosymbiont or endobiont is any organism that lives within the body or cells of another organism most often, though not always, in a mutualistic relationship. (The term endosymbiosis is from the Greek: ἔνδον endon "within", σύν syn "together" and βίωσις biosis "living".) Examples are nitrogen-fixing bacteria, which live in the root nodules of legumes, single-cell algae inside reef-building corals and bacterial endosymbionts that provide essential nutrients to insects.

Rafflesiaceae

Rafflesiaceae

The Rafflesiaceae are a family of rare parasitic plants comprising 36 species in 3 genera found in the tropical forests of east and southeast Asia, including Rafflesia arnoldii, which has the largest flowers of all plants. The plants are endoparasites of vines in the genus Tetrastigma (Vitaceae) and lack stems, leaves, roots, and any photosynthetic tissue. They rely entirely on their host plants for both water and nutrients, and only then emerge as flowers from the roots or lower stems of the host plants.

Phaseolus

Phaseolus

Phaseolus is a genus of herbaceous to woody annual and perennial vines in the family Fabaceae containing about 70 plant species, all native to the Americas, primarily Mesoamerica.

Saccharomyces cerevisiae

Saccharomyces cerevisiae

Saccharomyces cerevisiae is a species of yeast. The species has been instrumental in winemaking, baking, and brewing since ancient times. It is believed to have been originally isolated from the skin of grapes. It is one of the most intensively studied eukaryotic model organisms in molecular and cell biology, much like Escherichia coli as the model bacterium. It is the microorganism behind the most common type of fermentation. S. cerevisiae cells are round to ovoid, 5–10 μm in diameter. It reproduces by budding.

HhMAN1

HhMAN1

HhMAN1 is a gene in the genome of Hypothenemus hampei, a.k.a. coffee berry borer, which codes for mannanase, an enzyme used to digest galactomannan, a complex polysaccharide that is found in coffee beans. Because mannanase is not commonly found in similar beetles, and the characteristic of the gene is bacterial, the gene is thought to have originated from bacteria in the beetle's gut, and transposed to the beetle's genome through horizontal gene transfer (HGT). Although horizontal gene transfer from bacteria to eukaryotes have been known to occur, albeit rarely, the HhMAN1 is the first to have a known and beneficial function to the recipient.

Hypothenemus hampei

Hypothenemus hampei

Hypothenemus hampei, the coffee berry borer or coffee borer beetle, is a small beetle native to Africa. It is among the most harmful pests to coffee crops across the world where coffee is cultivated. Spanish common names of the insect include barrenador del café, gorgojo del café, and broca del café.

Oskar (gene)

Oskar (gene)

oskar is a gene required for the development of the Drosophila embryo. It defines the posterior pole during early embryogenesis. Its two isoforms, short and long, play different roles in Drosophila embryonic development. oskar was named after the main character from the Günter Grass novel The Tin Drum, who refuses to grow up.

Tardigrade

Tardigrade

Tardigrades, known colloquially as water bears or moss piglets, are a phylum of eight-legged segmented micro-animals. They were first described by the German zoologist Johann August Ephraim Goeze in 1773, who called them Kleiner Wasserbär. In 1777, the Italian biologist Lazzaro Spallanzani named them Tardigrada, which means "slow steppers".

Caenorhabditis

Caenorhabditis

Caenorhabditis is a genus of nematodes which live in bacteria-rich environments like compost piles, decaying dead animals and rotting fruit. The name comes from Greek: caeno- ; rhabditis = rod-like. In 1900, Maupas initially named the species Rhabditis elegans, Osche placed it in the subgenus Caenorhabditis in 1952, and in 1955, Dougherty raised Caenorhabditis to the status of genus.

Compounds found to promote horizontal gene transfer

Through research into the growing issue of antibiotic resistance[120] certain compounds have been observed to promote horizontal gene transfer.[121][122][123][124] Antibiotics given to bacteria at non-lethal levels have been known to be a cause of antibiotic resistance[124] but emerging research is now showing that certain non-antibiotic pharmaceuticals (ibuprofen, naproxen, gemfibrozil, diclofenac, propranolol, etc.) also have a role in promoting antibiotic resistance through their ability to promote horizontal gene transfer (HGT) of genes responsible for antibiotic resistance. The transfer of antibiotic resistance genes (ARGs) through conjugation is significantly accelerated when donor cells with plasmids and recipient cells are introduced to each other in the presence of one of the pharmaceuticals.[121] Non-antibiotic pharmaceuticals were also found to cause some responses in bacteria similar to those responses to antibiotics, such as increasing expression of the genes lexA, umuC, umuD and soxR involved in the bacteria's SOS response as well as other genes also expressed during exposure to antibiotics.[121] These findings are from 2021 and due to the widespread use of non-antibiotic pharmaceuticals, more research needs to be done in order to further understanding on the issue.[121]

Alongside non-antibiotic pharmaceuticals, other compounds relevant to antibiotic resistance have been tested such as malachite green, ethylbenzene, styrene, 2,4-dichloroaniline, trioxymethylene, o-xylene solutions, p-nitrophenol (PNP), p-aminophenol (PAP), and phenol (PhOH).[122][123] It is a global concern that ARGs have been found in wastewater treatment plants[122] Textile wastewater has been found to contain 3- to 13-fold higher abundance of mobile genetic elements than other samples of wastewater.[122] The cause of this is the organic compounds used for textile dying (o-xylene, ethylbenzene, trioxymethylene, styrene, 2,4-dichloroaniline, and malachite green)[122] raising the frequency of conjugative transfer when bacteria and plasmid (with donor) are introduced in the presence of these molecules.[122] When textile wastewater combines with wastewater from domestic sewage, the ARGs present in wastewater are transferred at a higher rate due to the addition of textile dyeing compounds increasing the occurrence of HGT.

Other organic pollutants commonly found in wastewater have been the subject of similar experiments.[123] A 2021 study used similar methods of  using plasmid in a donor and mixing that with a receptor in the presence of compound in order to test horizontal gene transfer of antibiotic resistance genes but this time in the presence of phenolic compounds.[123] Phenolic compounds are commonly found in wastewater and have been found to change functions and structures of the microbial communities during the wastewater treatment process.[123] Additionally, HGT increases in frequency in the presence of the compounds p-nitrophenol (PNP), p-aminophenol (PAP), and phenol. These compounds result in a 2- to 9-fold increase in HGT (p-nitrophenol being on the lower side of 2-fold increases and p-aminophenol and phenol having a maximum increase of 9-fold).[123] This increase in HGT is on average less than the compounds ibuprofen, naproxen, gemfibrozil, diclofenac, propranolol, o-xylene, ethylbenzene, trioxymethylene, styrene, 2,4-dichloroaniline, and malachite green[121][122] but their increases is still significant.[123] The study that came to this conclusion is similar to the study on horizontal gene transfer and non-antibiotic pharmaceuticals in that it was done in 2021 and leaves room for more research, specifically in the focus of the study which is activated sludge.[123]

Heavy metals have also been found to promote conjugative transfer of antibiotic resistance genes.[124] The paper that led to the discovery of this was done in 2017 during the emerging field of horizontal gene transfer assisting compound research.[124] Metals assist in the spread of antibiotic resistance through both co-resistance as well as cross-resistance mechanisms.[124] In quantities relevant to the environment, Cu(II), Ag(I), Cr(VI), and Zn(II) promote HGT from donor and receptor strains of E. coli.[124] The presence of these metals triggered SOS response from bacterial cells and made the cells more permeable. These are the mechanisms that make even low levels of heavy metal pollution in the environment impact HGT and therefore the spread of ARGs.

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Antimicrobial resistance

Antimicrobial resistance

Antimicrobial resistance (AMR) occurs when microbes evolve mechanisms that protect them from the effects of antimicrobials. All classes of microbes can evolve resistance. Fungi evolve antifungal resistance. Viruses evolve antiviral resistance. Protozoa evolve antiprotozoal resistance, and bacteria evolve antibiotic resistance. Bacteria that are considered extensively drug resistant (XDR) or totally drug-resistant (TDR) are sometimes referred to as a superbug. Although antimicrobial resistance is a naturally-occurring process, it is often the result of improper usage of the drugs and management of the infections.

Ibuprofen

Ibuprofen

Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID) that is used to relieve pain, fever, and inflammation. This includes painful menstrual periods, migraines, and rheumatoid arthritis. It may also be used to close a patent ductus arteriosus in a premature baby. It can be used by mouth or intravenously. It typically begins working within an hour.

Gemfibrozil

Gemfibrozil

Gemfibrozil, sold under the brand name Lopid among others, is a medication used to treat abnormal blood lipid levels. It is generally less preferred than statins. Use is recommended together with dietary changes and exercise. It is unclear if it changes the risk of heart disease. It is taken by mouth.

Diclofenac

Diclofenac

Diclofenac, sold under the brand name Voltaren, among others, is a nonsteroidal anti-inflammatory drug (NSAID) used to treat pain and inflammatory diseases such as gout. It is taken by mouth or rectally in a suppository, used by injection, or applied to the skin. Improvements in pain last for as much as eight hours. It is also available in combination with misoprostol in an effort to decrease stomach problems.

Bacterial conjugation

Bacterial conjugation

Bacterial conjugation is the transfer of genetic material between bacterial cells by direct cell-to-cell contact or by a bridge-like connection between two cells. This takes place through a pilus. It is a parasexual mode of reproduction in bacteria.

Malachite green

Malachite green

Malachite green is an organic compound that is used as a dyestuff and controversially as an antimicrobial in aquaculture. Malachite green is traditionally used as a dye for materials such as silk, leather, and paper. Despite its name the dye is not prepared from the mineral malachite; the name just comes from the similarity of color.

Ethylbenzene

Ethylbenzene

Ethylbenzene is an organic compound with the formula C6H5CH2CH3. It is a highly flammable, colorless liquid with an odor similar to that of gasoline. This monocyclic aromatic hydrocarbon is important in the petrochemical industry as an reaction intermediate in the production of styrene, the precursor to polystyrene, a common plastic material. In 2012, more than 99% of ethylbenzene produced was consumed in the production of styrene.

Dichloroaniline

Dichloroaniline

Dichloroanilines are chemical compounds which consist of an aniline ring substituted with two chlorine atoms and have the molecular formula C6H5Cl2N. There are six isomers, varying in the positions of the chlorine atoms around the ring relative to the amino group. As aniline derivatives, they are named with the amino group in position 1. They are all colorless, although commercial samples can appear colored due to the presence of impurities. Several derivatives are used in the production of dyes and herbicides.

1,3,5-Trioxane

1,3,5-Trioxane

1,3,5-Trioxane, sometimes also called trioxane or trioxin, is a chemical compound with molecular formula C3H6O3. It is a white, highly water-soluble solid with a chloroform-like odor. It is a stable cyclic trimer of formaldehyde, and one of the three trioxane isomers; its molecular backbone consists of a six-membered ring with three carbon atoms alternating with three oxygen atoms.

4-Nitrophenol

4-Nitrophenol

4-Nitrophenol is a phenolic compound that has a nitro group at the opposite position of the hydroxyl group on the benzene ring.

4-Aminophenol

4-Aminophenol

4-Aminophenol (or para-aminophenol or p-aminophenol) is an organic compound with the formula H2NC6H4OH. Typically available as a white powder, it is commonly used as a developer for black-and-white film, marketed under the name Rodinal.

Mobile genetic elements

Mobile genetic elements

Mobile genetic elements (MGEs) sometimes called selfish genetic elements are a type of genetic material that can move around within a genome, or that can be transferred from one species or replicon to another. MGEs are found in all organisms. In humans, approximately 50% of the genome is thought to be MGEs. MGEs play a distinct role in evolution. Gene duplication events can also happen through the mechanism of MGEs. MGEs can also cause mutations in protein coding regions, which alters the protein functions. These mechanisms can also rearrange genes in the host genome generating variation. These mechanism can increase fitness by gaining new or additional functions. An example of MGEs in evolutionary context are that virulence factors and antibiotic resistance genes of MGEs can be transported to share genetic code with neighboring bacteria. However, MGEs can also decrease fitness by introducing disease-causing alleles or mutations. The set of MGEs in an organism is called a mobilome, which is composed of a large number of plasmids, transposons and viruses.

Artificial horizontal gene transfer

Before it is transformed, a bacterium is susceptible to antibiotics. A plasmid can be inserted when the bacteria is under stress, and be incorporated into the bacterial DNA creating antibiotic resistance. When the plasmids are prepared they are inserted into the bacterial cell by either making pores in the plasma membrane with temperature extremes and chemical treatments, or making it semi permeable through the process of electrophoresis, in which electric currents create the holes in the membrane. After conditions return to normal the holes in the membrane close and the plasmids are trapped inside the bacteria where they become part of the genetic material and their genes are expressed by the bacteria.
Before it is transformed, a bacterium is susceptible to antibiotics. A plasmid can be inserted when the bacteria is under stress, and be incorporated into the bacterial DNA creating antibiotic resistance. When the plasmids are prepared they are inserted into the bacterial cell by either making pores in the plasma membrane with temperature extremes and chemical treatments, or making it semi permeable through the process of electrophoresis, in which electric currents create the holes in the membrane. After conditions return to normal the holes in the membrane close and the plasmids are trapped inside the bacteria where they become part of the genetic material and their genes are expressed by the bacteria.

Genetic engineering is essentially horizontal gene transfer, albeit with synthetic expression cassettes. The Sleeping Beauty transposon system[125] (SB) was developed as a synthetic gene transfer agent that was based on the known abilities of Tc1/mariner transposons to invade genomes of extremely diverse species.[126] The SB system has been used to introduce genetic sequences into a wide variety of animal genomes.[127][128]

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Gene therapy

Gene therapy

Gene therapy is a medical field which focuses on the genetic modification of cells to produce a therapeutic effect or the treatment of disease by repairing or reconstructing defective genetic material. The first attempt at modifying human DNA was performed in 1980, by Martin Cline, but the first successful nuclear gene transfer in humans, approved by the National Institutes of Health, was performed in May 1989. The first therapeutic use of gene transfer as well as the first direct insertion of human DNA into the nuclear genome was performed by French Anderson in a trial starting in September 1990. It is thought to be able to cure many genetic disorders or treat them over time.

Genetic engineering

Genetic engineering

Genetic engineering, also called genetic modification or genetic manipulation, is the modification and manipulation of an organism's genes using technology. It is a set of technologies used to change the genetic makeup of cells, including the transfer of genes within and across species boundaries to produce improved or novel organisms. New DNA is obtained by either isolating and copying the genetic material of interest using recombinant DNA methods or by artificially synthesising the DNA. A construct is usually created and used to insert this DNA into the host organism. The first recombinant DNA molecule was made by Paul Berg in 1972 by combining DNA from the monkey virus SV40 with the lambda virus. As well as inserting genes, the process can be used to remove, or "knock out", genes. The new DNA can be inserted randomly, or targeted to a specific part of the genome.

Sleeping Beauty transposon system

Sleeping Beauty transposon system

The Sleeping Beauty transposon system is a synthetic DNA transposon designed to introduce precisely defined DNA sequences into the chromosomes of vertebrate animals for the purposes of introducing new traits and to discover new genes and their functions. It is a Tc1/mariner-type system, with the transposase resurrected from multiple inactive fish sequences.

Tc1/mariner

Tc1/mariner

Tc1/mariner is a class and superfamily of interspersed repeats DNA transposons. The elements of this class are found in all animals, including humans. They can also be found in protists and bacteria.

Importance in evolution

Horizontal gene transfer is a potential confounding factor in inferring phylogenetic trees based on the sequence of one gene.[129] For example, given two distantly related bacteria that have exchanged a gene a phylogenetic tree including those species will show them to be closely related because that gene is the same even though most other genes are dissimilar. For this reason, it is often ideal to use other information to infer robust phylogenies such as the presence or absence of genes or, more commonly, to include as wide a range of genes for phylogenetic analysis as possible.

For example, the most common gene to be used for constructing phylogenetic relationships in prokaryotes is the 16S ribosomal RNA gene since its sequences tend to be conserved among members with close phylogenetic distances, but variable enough that differences can be measured. However, in recent years it has also been argued that 16s rRNA genes can also be horizontally transferred. Although this may be infrequent, the validity of 16s rRNA-constructed phylogenetic trees must be reevaluated.[130]

Biologist Johann Peter Gogarten suggests "the original metaphor of a tree no longer fits the data from recent genome research" therefore "biologists should use the metaphor of a mosaic to describe the different histories combined in individual genomes and use the metaphor of a net to visualize the rich exchange and cooperative effects of HGT among microbes".[38] There exist several methods to infer such phylogenetic networks.

Using single genes as phylogenetic markers, it is difficult to trace organismal phylogeny in the presence of horizontal gene transfer. Combining the simple coalescence model of cladogenesis with rare HGT horizontal gene transfer events suggest there was no single most recent common ancestor that contained all of the genes ancestral to those shared among the three domains of life. Each contemporary molecule has its own history and traces back to an individual molecule cenancestor. However, these molecular ancestors were likely to be present in different organisms at different times."[131]

Challenge to the tree of life

Horizontal gene transfer poses a possible challenge to the concept of the last universal common ancestor (LUCA) at the root of the tree of life first formulated by Carl Woese, which led him to propose the Archaea as a third domain of life.[132] Indeed, it was while examining the new three-domain view of life that horizontal gene transfer arose as a complicating issue: Archaeoglobus fulgidus was seen as an anomaly with respect to a phylogenetic tree based upon the encoding for the enzyme HMGCoA reductase—the organism in question is a definite Archaean, with all the cell lipids and transcription machinery that are expected of an Archaean, but whose HMGCoA genes are of bacterial origin.[132] Scientists are broadly agreed on symbiogenesis, that mitochondria in eukaryotes derived from alpha-proteobacterial cells and that chloroplasts came from ingested cyanobacteria, and other gene transfers may have affected early eukaryotes. (In contrast, multicellular eukaryotes have mechanisms to prevent horizontal gene transfer, including separated germ cells.) If there had been continued and extensive gene transfer, there would be a complex network with many ancestors, instead of a tree of life with sharply delineated lineages leading back to a LUCA.[132][133] However, a LUCA can be identified, so horizontal transfers must have been relatively limited.[134]

Phylogenetic information in HGT

It has been remarked that, despite the complications, the detection of horizontal gene transfers brings valuable phylogenetic and dating information.[135]

The potential of HGT to be used for dating phylogenies has recently been confirmed.[136][137]

The chromosomal organization of horizontal gene transfer

The acquisition of new genes has the potential to disorganize the other genetic elements and hinder the function of the bacterial cell, thus affecting the competitiveness of bacteria. Consequently, bacterial adaptation lies in a conflict between the advantages of acquiring beneficial genes, and the need to maintain the organization of the rest of its genome. Horizontally transferred genes are typically concentrated in only ~1% of the chromosome (in regions called hotspots). This concentration increases with genome size and with the rate of transfer. Hotspots diversify by rapid gene turnover; their chromosomal distribution depends on local contexts (neighboring core genes), and content in mobile genetic elements. Hotspots concentrate most changes in gene repertoires, reduce the trade-off between genome diversification and organization, and should be treasure troves of strain-specific adaptive genes. Most mobile genetic elements and antibiotic resistance genes are in hotspots, but many hotspots lack recognizable mobile genetic elements and exhibit frequent homologous recombination at flanking core genes. Overrepresentation of hotspots with fewer mobile genetic elements in naturally transformable bacteria suggests that homologous recombination and horizontal gene transfer are tightly linked in genome evolution.[138]

Genes

There is evidence for historical horizontal transfer of the following genes:

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Horizontal gene transfer in evolution

Horizontal gene transfer in evolution

Scientists trying to reconstruct evolutionary history have been challenged by the fact that genes can sometimes transfer between distant branches on the tree of life. This movement of genes can occur through horizontal gene transfer (HGT), scrambling the information on which biologists relied to reconstruct the phylogeny of organisms. Conversely, HGT can also help scientists to reconstruct and date the tree of life. Indeed, a gene transfer can be used as a phylogenetic marker, or as the proof of contemporaneity of the donor and recipient organisms, and as a trace of extinct biodiversity.

Phylogenetic tree

Phylogenetic tree

A phylogenetic tree is a branching diagram or a tree showing the evolutionary relationships among various biological species or other entities based upon similarities and differences in their physical or genetic characteristics. All life on Earth is part of a single phylogenetic tree, indicating common ancestry.

Prokaryote

Prokaryote

A prokaryote is a single-celled organism that lacks a nucleus and other membrane-bound organelles. The word prokaryote comes from the Greek πρό and κάρυον. In the two-empire system arising from the work of Édouard Chatton, prokaryotes were classified within the empire Prokaryota. But in the three-domain system, based upon molecular analysis, prokaryotes are divided into two domains: Bacteria and Archaea. Organisms with nuclei are placed in a third domain, Eukaryota. In biological evolution, prokaryotes are deemed to have arisen before eukaryotes.

16S ribosomal RNA

16S ribosomal RNA

16S ribosomal RNA is the RNA component of the 30S subunit of a prokaryotic ribosome. It binds to the Shine-Dalgarno sequence and provides most of the SSU structure.

Johann Peter Gogarten

Johann Peter Gogarten

Johann Peter Gogarten is a German-American biologist studying the early evolution of life. Born in Bad Oeynhausen, Germany, he studied plant physiology and membrane transport with Friedrich-Wilhelm Bentrup in Tübingen and Giessen. In 1987 he moved to the US as a postdoc to work with Lincoln Taiz at UC Santa Cruz. He currently is Distinguished Professor of Molecular and Cell Biology at the University of Connecticut in Storrs, CT.

Phylogenetic network

Phylogenetic network

A phylogenetic network is any graph used to visualize evolutionary relationships between nucleotide sequences, genes, chromosomes, genomes, or species. They are employed when reticulation events such as hybridization, horizontal gene transfer, recombination, or gene duplication and loss are believed to be involved. They differ from phylogenetic trees by the explicit modeling of richly linked networks, by means of the addition of hybrid nodes instead of only tree nodes. Phylogenetic trees are a subset of phylogenetic networks. Phylogenetic networks can be inferred and visualised with software such as SplitsTree, the R-package, phangorn, and, more recently, Dendroscope. A standard format for representing phylogenetic networks is a variant of Newick format which is extended to support networks as well as trees.

Coalescent theory

Coalescent theory

Coalescent theory is a model of how alleles sampled from a population may have originated from a common ancestor. In the simplest case, coalescent theory assumes no recombination, no natural selection, and no gene flow or population structure, meaning that each variant is equally likely to have been passed from one generation to the next. The model looks backward in time, merging alleles into a single ancestral copy according to a random process in coalescence events. Under this model, the expected time between successive coalescence events increases almost exponentially back in time. Variance in the model comes from both the random passing of alleles from one generation to the next, and the random occurrence of mutations in these alleles.

Cladogenesis

Cladogenesis

Cladogenesis is an evolutionary splitting of a parent species into two distinct species, forming a clade.

Most recent common ancestor

Most recent common ancestor

In biology and genetic genealogy, the most recent common ancestor (MRCA), also known as the last common ancestor (LCA) or concestor, of a set of organisms is the most recent individual from which all the organisms of the set are descended. The term is also used in reference to the ancestry of groups of genes (haplotypes) rather than organisms.

Life

Life

Life is a quality that distinguishes matter that has biological processes, such as signaling and self-sustaining processes, from matter that does not, and is defined by the capacity for growth, reaction to stimuli, metabolism, energy transformation, and reproduction. Various forms of life exist, such as plants, animals, fungi, protists, archaea, and bacteria. Biology is the science that studies life.

Molecule

Molecule

A molecule is a group of two or more atoms held together by attractive forces known as chemical bonds; depending on context, the term may or may not include ions which satisfy this criterion. In quantum physics, organic chemistry, and biochemistry, the distinction from ions is dropped and molecule is often used when referring to polyatomic ions.

Last universal common ancestor

Last universal common ancestor

The last universal common ancestor (LUCA) is the most recent population from which all organisms now living on Earth share common descent—the most recent common ancestor of all current life on Earth. This includes all cellular organisms; the origins of viruses are unclear but they share the same genetic code. LUCA probably harboured a variety of viruses. The LUCA is not the first life on Earth, but rather the latest form ancestral to all existing life.

Source: "Horizontal gene transfer", Wikipedia, Wikimedia Foundation, (2023, February 26th), https://en.wikipedia.org/wiki/Horizontal_gene_transfer.

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References
  1. ^ Ochman H, Lawrence JG, Groisman EA (May 2000). "Lateral gene transfer and the nature of bacterial innovation". Nature. 405 (6784): 299–304. Bibcode:2000Natur.405..299O. doi:10.1038/35012500. PMID 10830951. S2CID 85739173.
  2. ^ Dunning Hotopp JC (April 2011). "Horizontal gene transfer between bacteria and animals". Trends in Genetics. 27 (4): 157–63. doi:10.1016/j.tig.2011.01.005. PMC 3068243. PMID 21334091.
  3. ^ Robinson KM, Sieber KB, Dunning Hotopp JC (October 2013). "A review of bacteria-animal lateral gene transfer may inform our understanding of diseases like cancer". PLOS Genetics. 9 (10): e1003877. doi:10.1371/journal.pgen.1003877. PMC 3798261. PMID 24146634.
  4. ^ Keeling PJ, Palmer JD (August 2008). "Horizontal gene transfer in eukaryotic evolution". Nature Reviews. Genetics. 9 (8): 605–18. doi:10.1038/nrg2386. PMID 18591983. S2CID 213613.
  5. ^ a b c d e f Gyles C, Boerlin P (March 2014). "Horizontally transferred genetic elements and their role in pathogenesis of bacterial disease". Veterinary Pathology. 51 (2): 328–40. doi:10.1177/0300985813511131. PMID 24318976. S2CID 206510894.
  6. ^ Vaux F, Trewick SA, Morgan-Richards M (2017). "Speciation through the looking-glass". Biological Journal of the Linnean Society. 120 (2): 480–488. doi:10.1111/bij.12872.
  7. ^ Ochman, H., Lerat, E., & Daubin, V. (2005). Examining bacterial species under the specter of gene transfer and exchange. Proceedings of the National Academy of Sciences, 102(suppl_1), 6595-6599.
  8. ^ Huddleston JR (2014). "Horizontal gene transfer in the human gastrointestinal tract: potential spread of antibiotic resistance genes". Infection and Drug Resistance. 7: 167–176. doi:10.2147/idr.s48820. PMC 4073975. PMID 25018641.
  9. ^ Koonin EV, Makarova KS, Aravind L (2001). "Horizontal gene transfer in prokaryotes: quantification and classification". Annual Review of Microbiology. 55 (1): 709–42. doi:10.1146/annurev.micro.55.1.709. PMC 4781227. PMID 11544372.
  10. ^ Nielsen KM (1998). "Barriers to horizontal gene transfer by natural transformation in soil bacteria". APMIS. 84 (S84): 77–84. doi:10.1111/j.1600-0463.1998.tb05653.x. PMID 9850687. S2CID 26490197.
  11. ^ McGowan C, Fulthorpe R, Wright A, Tiedje JM (October 1998). "Evidence for interspecies gene transfer in the evolution of 2,4-dichlorophenoxyacetic acid degraders". Applied and Environmental Microbiology. 64 (10): 4089–92. Bibcode:1998ApEnM..64.4089M. doi:10.1128/AEM.64.10.4089-4092.1998. PMC 106609. PMID 9758850.
  12. ^ a b Keen EC (December 2012). "Paradigms of pathogenesis: targeting the mobile genetic elements of disease". Frontiers in Cellular and Infection Microbiology. 2: 161. doi:10.3389/fcimb.2012.00161. PMC 3522046. PMID 23248780.
  13. ^ Naik GA, Bhat LN, Chpoade BA, Lynch JM (1994). "Transfer of broad-host-range antibiotic resistance plasmids in soil microcosms". Curr. Microbiol. 28 (4): 209–215. doi:10.1007/BF01575963. S2CID 21015053.
  14. ^ Varga M, Kuntová L, Pantůček R, Mašlaňová I, Růžičková V, Doškař J (July 2012). "Efficient transfer of antibiotic resistance plasmids by transduction within methicillin-resistant Staphylococcus aureus USA300 clone". FEMS Microbiology Letters. 332 (2): 146–52. doi:10.1111/j.1574-6968.2012.02589.x. PMID 22553940.
  15. ^ Varga M, Pantu Ček R, Ru Žičková V, Doškař J (January 2016). "Molecular characterization of a new efficiently transducing bacteriophage identified in meticillin-resistant Staphylococcus aureus". The Journal of General Virology. 97 (1): 258–268. doi:10.1099/jgv.0.000329. PMID 26537974.
  16. ^ Cairns J, Ruokolainen L, Hultman J, Tamminen M, Virta M, Hiltunen T (2018-04-19). "Ecology determines how low antibiotic concentration impacts community composition and horizontal transfer of resistance genes". Communications Biology. 1 (1): 35. doi:10.1038/s42003-018-0041-7. PMC 6123812. PMID 30271921.
  17. ^ Zhou H, Beltrán JF, Brito IL (October 2021). "Functions predict horizontal gene transfer and the emergence of antibiotic resistance". Science Advances. 7 (43): eabj5056. Bibcode:2021SciA....7.5056Z. doi:10.1126/sciadv.abj5056. PMC 8535800. PMID 34678056.
  18. ^ Sieber KB, Bromley RE, Dunning Hotopp JC (September 2017). "Lateral gene transfer between prokaryotes and eukaryotes". Experimental Cell Research. 358 (2): 421–426. doi:10.1016/j.yexcr.2017.02.009. PMC 5550378. PMID 28189637.
  19. ^ Gabaldón T (October 2021). "Origin and Early Evolution of the Eukaryotic Cell". Annual Review of Microbiology. 75 (1): 631–647. doi:10.1146/annurev-micro-090817-062213. PMID 34343017. S2CID 236916203.
  20. ^ Kubyshkin V, Acevedo-Rocha CG, Budisa N (February 2018). "On universal coding events in protein biogenesis". Bio Systems. 164: 16–25. doi:10.1016/j.biosystems.2017.10.004. PMID 29030023.
  21. ^ Griffith F (January 1928). "The Significance of Pneumococcal Types". The Journal of Hygiene. Cambridge University Press. 27 (2): 113–59. doi:10.1017/S0022172400031879. JSTOR 4626734. PMC 2167760. PMID 20474956.
  22. ^ Lorenz MG, Wackernagel W (September 1994). "Bacterial gene transfer by natural genetic transformation in the environment". Microbiological Reviews. 58 (3): 563–602. doi:10.1128/MMBR.58.3.563-602.1994. PMC 372978. PMID 7968924.
  23. ^ Downie AW (November 1972). "Pneumococcal transformation--a backward view. Fourth Griffith Memorial Lecture" (PDF). Journal of General Microbiology. 73 (1): 1–11. doi:10.1099/00221287-73-1-1. PMID 4143929.
  24. ^ Freeman VJ (June 1951). "Studies on the virulence of bacteriophage-infected strains of Corynebacterium diphtheriae". Journal of Bacteriology. 61 (6): 675–88. doi:10.1128/JB.61.6.675-688.1951. PMC 386063. PMID 14850426.
  25. ^ Phillip Marguilies "Epidemics: Deadly diseases throughout history". Rosen, New York. 2005.
  26. ^ André Lwoff (1965). "Interaction among Virus, Cell, and Organism". Nobel Lecture for the Nobel Prize in Physiology or Medicine.
  27. ^ Ochiai K, Yamanaka T, Kimura K, Sawada O (1959). "Inheritance of drug resistance (and its transfer) between Shigella strains and Between Shigella and E. coli strains". Hihon Iji Shimpor (in Japanese). 1861: 34.
  28. ^ Akiba T, Koyama K, Ishiki Y, Kimura S, Fukushima T (April 1960). "On the mechanism of the development of multiple-drug-resistant clones of Shigella". Japanese Journal of Microbiology. 4 (2): 219–27. doi:10.1111/j.1348-0421.1960.tb00170.x. PMID 13681921.
  29. ^ Syvanen M (January 1985). "Cross-species gene transfer; implications for a new theory of evolution" (PDF). Journal of Theoretical Biology. 112 (2): 333–43. Bibcode:1985JThBi.112..333S. doi:10.1016/S0022-5193(85)80291-5. PMID 2984477.
  30. ^ Jain R, Rivera MC, Lake JA (March 1999). "Horizontal gene transfer among genomes: the complexity hypothesis". Proceedings of the National Academy of Sciences of the United States of America. 96 (7): 3801–6. Bibcode:1999PNAS...96.3801J. doi:10.1073/pnas.96.7.3801. PMC 22375. PMID 10097118.
  31. ^ Rivera MC, Lake JA (September 2004). "The ring of life provides evidence for a genome fusion origin of eukaryotes" (PDF). Nature. 431 (7005): 152–5. Bibcode:2004Natur.431..152R. doi:10.1038/nature02848. PMID 15356622. S2CID 4349149. Archived from the original (PDF) on 2007-09-27.
  32. ^ Bapteste E, Susko E, Leigh J, MacLeod D, Charlebois RL, Doolittle WF (May 2005). "Do orthologous gene phylogenies really support tree-thinking?". BMC Evolutionary Biology. 5 (1): 33. doi:10.1186/1471-2148-5-33. PMC 1156881. PMID 15913459.
  33. ^ Le Page M (2016-03-17). "Farmers may have been accidentally making GMOs for millennia". The New Scientist. Retrieved 2016-07-11.
  34. ^ Gasmi L, Boulain H, Gauthier J, Hua-Van A, Musset K, Jakubowska AK, et al. (September 2015). "Recurrent Domestication by Lepidoptera of Genes from Their Parasites Mediated by Bracoviruses". PLOS Genetics. 11 (9): e1005470. doi:10.1371/journal.pgen.1005470. PMC 4574769. PMID 26379286.
  35. ^ Yong E (2010-02-14). "Genes from Chagas parasite can transfer to humans and be passed on to children". National Geographic. Retrieved 2016-07-13.
  36. ^ Riley DR, Sieber KB, Robinson KM, White JR, Ganesan A, Nourbakhsh S, Dunning Hotopp JC (2013). "Bacteria-human somatic cell lateral gene transfer is enriched in cancer samples". PLOS Computational Biology. 9 (6): e1003107. Bibcode:2013PLSCB...9E3107R. doi:10.1371/journal.pcbi.1003107. PMC 3688693. PMID 23840181.
  37. ^ Richardson AO, Palmer JD (2007). "Horizontal gene transfer in plants" (PDF). Journal of Experimental Botany. 58 (1): 1–9. doi:10.1093/jxb/erl148. PMID 17030541. Archived from the original (PDF) on 2007-09-27.
  38. ^ a b Gogarten, Peter (2000). "Horizontal Gene Transfer: A New Paradigm for Biology". Esalen Center for Theory and Research Conference. Archived from the original on 2012-07-21. Retrieved 2007-03-18.
  39. ^ Kenneth Todar. "Bacterial Resistance to Antibiotics". The Microbial World: Lectures in Microbiology, Department of Bacteriology, University of Wisconsin-Madison. Archived from the original on January 15, 2012. Retrieved January 6, 2012.
  40. ^ Stanley Maloy (July 15, 2002). "Horizontal Gene Transfer". San Diego State University. Retrieved January 6, 2012.
  41. ^ a b c d e Stearns, S. C., & Hoekstra, R. F. (2005). Evolution: An introduction (2nd ed.). Oxford, NY: Oxford Univ. Press. pp. 38-40.
  42. ^ Renner SS, Bellot S (2012). "Horizontal Gene Transfer in Eukaryotes: Fungi-to-Plant and Plant-to-Plant Transfers of Organellar DNA". Genomics of Chloroplasts and Mitochondria. Advances in Photosynthesis and Respiration. Vol. 35. Springer Science+Business Media B.V. pp. 223–235. doi:10.1007/978-94-007-2920-9_10. ISBN 978-94-007-2919-3.
  43. ^ Maxmen A (2010). "Virus-like particles speed bacterial evolution". Nature. doi:10.1038/news.2010.507.
  44. ^ a b c d e f g Schaack S, Gilbert C, Feschotte C (September 2010). "Promiscuous DNA: horizontal transfer of transposable elements and why it matters for eukaryotic evolution". Trends in Ecology & Evolution. 25 (9): 537–46. doi:10.1016/j.tree.2010.06.001. PMC 2940939. PMID 20591532.
  45. ^ a b Dupeyron M, Leclercq S, Cerveau N, Bouchon D, Gilbert C (January 2014). "Horizontal transfer of transposons between and within crustaceans and insects". Mobile DNA. 5 (1): 4. doi:10.1186/1759-8753-5-4. PMC 3922705. PMID 24472097.
  46. ^ a b c El Baidouri M, Carpentier MC, Cooke R, Gao D, Lasserre E, Llauro C, et al. (May 2014). "Widespread and frequent horizontal transfers of transposable elements in plants". Genome Research. 24 (5): 831–8. doi:10.1101/gr.164400.113. PMC 4009612. PMID 24518071.
  47. ^ a b c Ivancevic AM, Walsh AM, Kortschak RD, Adelson DL (December 2013). "Jumping the fine LINE between species: horizontal transfer of transposable elements in animals catalyses genome evolution". BioEssays. 35 (12): 1071–82. doi:10.1002/bies.201300072. PMID 24003001. S2CID 6968210.
  48. ^ a b Wallau GL, Ortiz MF, Loreto EL (2012). "Horizontal transposon transfer in eukarya: detection, bias, and perspectives". Genome Biology and Evolution. 4 (8): 689–99. doi:10.1093/gbe/evs055. PMC 3516303. PMID 22798449.
  49. ^ La Scola B, Desnues C, Pagnier I, Robert C, Barrassi L, Fournous G, et al. (September 2008). "The virophage as a unique parasite of the giant mimivirus". Nature. 455 (7209): 100–4. Bibcode:2008Natur.455..100L. doi:10.1038/nature07218. PMID 18690211. S2CID 4422249.
  50. ^ Pearson H (August 2008). "'Virophage' suggests viruses are alive". Nature. 454 (7205): 677. Bibcode:2008Natur.454..677P. doi:10.1038/454677a. PMID 18685665.
  51. ^ a b Bejarano ER, Khashoggi A, Witty M, Lichtenstein C (January 1996). "Integration of multiple repeats of geminiviral DNA into the nuclear genome of tobacco during evolution". Proceedings of the National Academy of Sciences of the United States of America. 93 (2): 759–64. Bibcode:1996PNAS...93..759B. doi:10.1073/pnas.93.2.759. PMC 40128. PMID 8570630.
  52. ^ Barlow M (2009). "What antimicrobial resistance has taught us about horizontal gene transfer". Horizontal Gene Transfer. Methods in Molecular Biology. Vol. 532. pp. 397–411. doi:10.1007/978-1-60327-853-9_23. ISBN 978-1-60327-852-2. PMID 19271198.
  53. ^ Hawkey PM, Jones AM (September 2009). "The changing epidemiology of resistance". The Journal of Antimicrobial Chemotherapy. 64 (Suppl 1): i3-10. doi:10.1093/jac/dkp256. PMID 19675017.
  54. ^ Francino MP, ed. (2012). Horizontal Gene Transfer in Microorganisms. Caister Academic Press. ISBN 978-1-908230-10-2.
  55. ^ Strauch E, Lurz R, Beutin L (December 2001). "Characterization of a Shiga toxin-encoding temperate bacteriophage of Shigella sonnei". Infection and Immunity. 69 (12): 7588–95. doi:10.1128/IAI.69.12.7588-7595.2001. PMC 98851. PMID 11705937.
  56. ^ Johnson CM, Grossman AD (November 2015). "Integrative and Conjugative Elements (ICEs): What They Do and How They Work". Annual Review of Genetics. 42 (1): 577–601. doi:10.1146/annurev-genet-112414-055018. PMC 5180612. PMID 26473380.
  57. ^ Oliveira PH, Touchon M, Rocha EP (September 2014). "The interplay of restriction-modification systems with mobile genetic elements and their prokaryotic hosts". Nucleic Acids Research. 49 (16): 10618–10631. doi:10.1093/nar/gku734. PMC 4176335. PMID 25120263.
  58. ^ Auchtung JM, Lee CA, Garrison KL, Grossman AD (June 2007). "Identification and characterization of the immunity repressor (ImmR) that controls the mobile genetic element ICE Bs1 of Bacillus subtilis". PLOS Genet. 64 (6): 1515–1528. doi:10.1111/j.1365-2958.2007.05748.x. PMC 3320793. PMID 17511812.
  59. ^ Tirumalai MR, Fox GE (September 2013). "An ICEBs1-like element may be associated with the extreme radiation and desiccation resistance of Bacillus pumilus SAFR-032 spores". Extremophiles. 17 (5): 767–774. doi:10.1007/s00792-013-0559-z. PMID 23812891. S2CID 8675124.
  60. ^ Link L, Sawyer J, Venkateswaran K, Nicholson W (February 2004). "Extreme spore UV resistance of Bacillus pumilus isolates obtained from an ultraclean Spacecraft Assembly Facility". Microb Ecol. 47 (2): 159–163. doi:10.1007/s00248-003-1029-4. PMID 14502417. S2CID 13416635.
  61. ^ Newcombe DA, Schuerger AC, Benardini JN, Dickinson D, Tanner R, Venkateswaran K (December 2005). "Survival of spacecraft-associated microorganisms under simulated martian UV irradiation". Appl Environ Microbiol. 71 (12): 8147–8156. Bibcode:2005ApEnM..71.8147N. doi:10.1128/AEM.71.12.8147-8156.2005. PMC 1317311. PMID 16332797.
  62. ^ Kempf MJ, Chen F, Kern R, Venkateswaran K (June 2005). "Recurrent isolation of hydrogen peroxide-resistant spores of Bacillus pumilus from a spacecraft assembly facility". Astrobiology. 5 (3): 391–405. Bibcode:2005AsBio...5..391K. doi:10.1089/ast.2005.5.391. PMID 15941382.
  63. ^ Biel SW, Hartl DL (June 1983). "Evolution of transposons: natural selection for Tn5 in Escherichia coli K12". Genetics. 103 (4): 581–592. doi:10.1093/genetics/103.4.581. PMC 1202041. PMID 6303898.
  64. ^ Chao L, Vargas C, Spear BB, Cox EC (1983). "Transposable elements as mutator genes in evolution". Nature. 303 (5918): 633–635. Bibcode:1983Natur.303..633C. doi:10.1038/303633a0. PMC 1202041. PMID 6303898.
  65. ^ Tirumalai MR, Karouia F, Tran Q, Stepanov VG, Bruce RJ, Ott M, Pierson DL, Fox GE (May 2017). "The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic". NPJ Microgravity. 3 (15): 15. doi:10.1038/s41526-017-0020-1. PMC 5460176. PMID 28649637.
  66. ^ Tirumalai MR, Karouia F, Tran Q, Stepanov VG, Bruce RJ, Ott M, Pierson DL, Fox GE (January 2019). "Evaluation of acquired antibiotic resistance in Escherichia coli exposed to long-term low-shear modeled microgravity and background antibiotic exposure". mBio. 10 (e02637-18). doi:10.1128/mBio.02637-18. PMC 6336426. PMID 30647159.
  67. ^ Ginolhac, A., Jarrin, C., Robe, P., Perrière, G., Vogel, T. M., Simonet, P., & Nalin, R. (2005). Type I polyketide synthases may have evolved through horizontal gene transfer. Journal of Molecular Evolution, 60(6), 716-725.
  68. ^ Gross, H., & Loper, J. E. (2009). Genomics of secondary metabolite production by Pseudomonas spp. Natural product reports, 26(11), 1408-1446.
  69. ^ Chen I, Dubnau D (March 2004). "DNA uptake during bacterial transformation". Nature Reviews. Microbiology. 2 (3): 241–9. doi:10.1038/nrmicro844. PMID 15083159. S2CID 205499369.
  70. ^ a b Johnsborg O, Eldholm V, Håvarstein LS (December 2007). "Natural genetic transformation: prevalence, mechanisms and function". Research in Microbiology. 158 (10): 767–78. doi:10.1016/j.resmic.2007.09.004. PMID 17997281.
  71. ^ Solomon JM, Grossman AD (April 1996). "Who's competent and when: regulation of natural genetic competence in bacteria". Trends in Genetics. 12 (4): 150–5. doi:10.1016/0168-9525(96)10014-7. PMID 8901420.
  72. ^ Michod RE, Bernstein H, Nedelcu AM (May 2008). "Adaptive value of sex in microbial pathogens" (PDF). Infection, Genetics and Evolution. 8 (3): 267–85. doi:10.1016/j.meegid.2008.01.002. PMID 18295550.
  73. ^ Keen EC, Bliskovsky VV, Malagon F, Baker JD, Prince JS, Klaus JS, Adhya SL (January 2017). "Novel "Superspreader" Bacteriophages Promote Horizontal Gene Transfer by Transformation". mBio. 8 (1): e02115-16. doi:10.1128/mBio.02115-16. PMC 5241400. PMID 28096488.
  74. ^ a b Gray TA, Krywy JA, Harold J, Palumbo MJ, Derbyshire KM (July 2013). "Distributive conjugal transfer in mycobacteria generates progeny with meiotic-like genome-wide mosaicism, allowing mapping of a mating identity locus". PLOS Biology. 11 (7): e1001602. doi:10.1371/journal.pbio.1001602. PMC 3706393. PMID 23874149.
  75. ^ Derbyshire KM, Gray TA (2014). "Distributive Conjugal Transfer: New Insights into Horizontal Gene Transfer and Genetic Exchange in Mycobacteria". Microbiology Spectrum. 2 (1): 61–79. doi:10.1128/microbiolspec.MGM2-0022-2013. PMC 4259119. PMID 25505644.
  76. ^ a b c Fröls S, Ajon M, Wagner M, Teichmann D, Zolghadr B, Folea M, et al. (November 2008). "UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation" (PDF). Molecular Microbiology. 70 (4): 938–52. doi:10.1111/j.1365-2958.2008.06459.x. PMID 18990182.
  77. ^ Allers T (November 2011). "Swapping genes to survive - a new role for archaeal type IV pili". Molecular Microbiology. 82 (4): 789–91. doi:10.1111/j.1365-2958.2011.07860.x. PMID 21992544.
  78. ^ a b c d Ajon M, Fröls S, van Wolferen M, Stoecker K, Teichmann D, Driessen AJ, et al. (November 2011). "UV-inducible DNA exchange in hyperthermophilic archaea mediated by type IV pili" (PDF). Molecular Microbiology. 82 (4): 807–17. doi:10.1111/j.1365-2958.2011.07861.x. PMID 21999488.
  79. ^ Fröls S, White MF, Schleper C (February 2009). "Reactions to UV damage in the model archaeon Sulfolobus solfataricus". Biochemical Society Transactions. 37 (Pt 1): 36–41. doi:10.1042/BST0370036. PMID 19143598.
  80. ^ Grogan DW (June 1996). "Exchange of genetic markers at extremely high temperatures in the archaeon Sulfolobus acidocaldarius". Journal of Bacteriology. 178 (11): 3207–11. doi:10.1128/jb.178.11.3207-3211.1996. PMC 178072. PMID 8655500.
  81. ^ Wood ER, Ghané F, Grogan DW (September 1997). "Genetic responses of the thermophilic archaeon Sulfolobus acidocaldarius to short-wavelength UV light". Journal of Bacteriology. 179 (18): 5693–8. doi:10.1128/jb.179.18.5693-5698.1997. PMC 179455. PMID 9294423.
  82. ^ Reilly MS, Grogan DW (February 2002). "Biological effects of DNA damage in the hyperthermophilic archaeon Sulfolobus acidocaldarius". FEMS Microbiology Letters. 208 (1): 29–34. doi:10.1016/s0378-1097(01)00575-4. PMID 11934490.
  83. ^ a b van Wolferen M, Ajon M, Driessen AJ, Albers SV (December 2013). "Molecular analysis of the UV-inducible pili operon from Sulfolobus acidocaldarius". MicrobiologyOpen. 2 (6): 928–37. doi:10.1002/mbo3.128. PMC 3892339. PMID 24106028.
  84. ^ van Wolferen M, Ma X, Albers SV (September 2015). "DNA Processing Proteins Involved in the UV-Induced Stress Response of Sulfolobales". Journal of Bacteriology. 197 (18): 2941–51. doi:10.1128/JB.00344-15. PMC 4542170. PMID 26148716.
  85. ^ Melcher U (2001). "Molecular genetics: Horizontal gene transfer". Stillwater, Oklahoma USA: Oklahoma State University. Archived from the original on 2016-03-04. Retrieved 2015-08-20.
  86. ^ Blanchard JL, Lynch M (July 2000). "Organellar genes: why do they end up in the nucleus?". Trends in Genetics. 16 (7): 315–20. doi:10.1016/S0168-9525(00)02053-9. PMID 10858662. Discusses theories on how mitochondria and chloroplast genes are transferred into the nucleus, and also what steps a gene needs to go through in order to complete this process.
  87. ^ Davis CC, Wurdack KJ (July 2004). "Host-to-parasite gene transfer in flowering plants: phylogenetic evidence from Malpighiales". Science. 305 (5684): 676–8. Bibcode:2004Sci...305..676D. doi:10.1126/science.1100671. PMID 15256617. S2CID 16180594.
  88. ^ Nickrent DL, Blarer A, Qiu YL, Vidal-Russell R, Anderson FE (October 2004). "Phylogenetic inference in Rafflesiales: the influence of rate heterogeneity and horizontal gene transfer". BMC Evolutionary Biology. 4 (1): 40. doi:10.1186/1471-2148-4-40. PMC 528834. PMID 15496229.
  89. ^ Woloszynska M, Bocer T, Mackiewicz P, Janska H (November 2004). "A fragment of chloroplast DNA was transferred horizontally, probably from non-eudicots, to mitochondrial genome of Phaseolus". Plant Molecular Biology. 56 (5): 811–20. doi:10.1007/s11103-004-5183-y. PMID 15803417. S2CID 14198321.
  90. ^ Hall C, Brachat S, Dietrich FS (June 2005). "Contribution of horizontal gene transfer to the evolution of Saccharomyces cerevisiae". Eukaryotic Cell. 4 (6): 1102–15. doi:10.1128/EC.4.6.1102-1115.2005. PMC 1151995. PMID 15947202.
  91. ^ Quispe-Huamanquispe DG, Gheysen G, Kreuze JF (2017). "Agrobacterium T-DNAs". Frontiers in Plant Science. 8: 2015. doi:10.3389/fpls.2017.02015. PMC 5705623. PMID 29225610.
  92. ^ Lee Phillips M (2012). "Bacterial gene helps coffee beetle get its fix". Nature. doi:10.1038/nature.2012.10116. S2CID 211729274.
  93. ^ Acuña R, Padilla BE, Flórez-Ramos CP, Rubio JD, Herrera JC, Benavides P, et al. (March 2012). "Adaptive horizontal transfer of a bacterial gene to an invasive insect pest of coffee". Proceedings of the National Academy of Sciences of the United States of America. 109 (11): 4197–202. Bibcode:2012PNAS..109.4197A. doi:10.1073/pnas.1121190109. PMC 3306691. PMID 22371593.
  94. ^ Blondel L, Jones ET, Extavour GC (Feb 2020). "Bacterial contribution to genesis of the novel germ line determinant oskar". eLife. 24 (9): e45539. doi:10.7554/eLife.45539. PMC 7250577. PMID 32091394.
  95. ^ Traci Watson (15 November 2012). "Bdelloids Surviving on Borrowed DNA". Science/AAAS News.
  96. ^ Koutsovoulos G, Kumar S, Laetsch DR, Stevens L, Daub J, Conlon C, et al. (May 2016). "No evidence for extensive horizontal gene transfer in the genome of the tardigrade Hypsibius dujardini". Proceedings of the National Academy of Sciences of the United States of America. 113 (18): 5053–8. Bibcode:2016PNAS..113.5053K. doi:10.1073/pnas.1600338113. PMC 4983863. PMID 27035985.
  97. ^ Crisp A, Boschetti C, Perry M, Tunnacliffe A, Micklem G (March 2015). "Expression of multiple horizontally acquired genes is a hallmark of both vertebrate and invertebrate genomes". Genome Biology. 16 (1): 50. doi:10.1186/s13059-015-0607-3. PMC 4358723. PMID 25785303.
  98. ^ Madhusoodanan J (2015-03-12). "Horizontal Gene Transfer a Hallmark of Animal Genomes?". The Scientist. Retrieved 2016-07-14.
  99. ^ Daugavet MA, Shabelnikov S, Shumeev A, Shaposhnikova T, Adonin LS, Podgornaya O (2019-01-19). "Features of a novel protein, rusticalin, from the ascidian Styela rustica reveal ancestral horizontal gene transfer event". Mobile DNA. 10 (1): 4. doi:10.1186/s13100-019-0146-7. PMC 6339383. PMID 30675192.
  100. ^ Redrejo-Rodríguez M, Muñoz-Espín D, Holguera I, Mencía M, Salas M (November 2012). "Functional eukaryotic nuclear localization signals are widespread in terminal proteins of bacteriophages". Proceedings of the National Academy of Sciences of the United States of America. 109 (45): 18482–7. Bibcode:2012PNAS..10918482R. doi:10.1073/pnas.1216635109. PMC 3494942. PMID 23091024.
  101. ^ Kondo N, Nikoh N, Ijichi N, Shimada M, Fukatsu T (October 2002). "Genome fragment of Wolbachia endosymbiont transferred to X chromosome of host insect". Proceedings of the National Academy of Sciences of the United States of America. 99 (22): 14280–5. Bibcode:2002PNAS...9914280K. doi:10.1073/pnas.222228199. PMC 137875. PMID 12386340.
  102. ^ Dunning Hotopp JC, Clark ME, Oliveira DC, Foster JM, Fischer P, Muñoz Torres MC, et al. (September 2007). "Widespread lateral gene transfer from intracellular bacteria to multicellular eukaryotes". Science. 317 (5845): 1753–6. Bibcode:2007Sci...317.1753H. doi:10.1126/science.1142490. PMID 17761848. S2CID 10787254.
  103. ^ Sloan, D. B., Nakabachi, A., Richards, S., Qu, J., Murali, S. C., Gibbs, R. A., & Moran, N. A. (2014). Parallel histories of horizontal gene transfer facilitated extreme reduction of endosymbiont genomes in sap-feeding insects. Molecular biology and evolution, 31(4), 857-871.
  104. ^ Yoshida S, Maruyama S, Nozaki H, Shirasu K (May 2010). "Horizontal gene transfer by the parasitic plant Striga hermonthica". Science. 328 (5982): 1128. Bibcode:2010Sci...328.1128Y. doi:10.1126/science.1187145. PMID 20508124. S2CID 39376164.
  105. ^ Carl Zimmer (April 17, 2014). "Plants That Practice Genetic Engineering". New York Times.
  106. ^ Schwartz JA, Curtis NE, Pierce SK (December 2014). "FISH labeling reveals a horizontally transferred algal (Vaucheria litorea) nuclear gene on a sea slug (Elysia chlorotica) chromosome". The Biological Bulletin. 227 (3): 300–12. doi:10.1086/BBLv227n3p300. PMID 25572217. S2CID 21742354.
  107. ^ Rauch C, Vries J, Rommel S, Rose LE, Woehle C, Christa G, et al. (August 2015). "Why It Is Time to Look Beyond Algal Genes in Photosynthetic Slugs". Genome Biology and Evolution. 7 (9): 2602–7. doi:10.1093/gbe/evv173. PMC 4607529. PMID 26319575.
  108. ^ Bhattacharya D, Pelletreau KN, Price DC, Sarver KE, Rumpho ME (August 2013). "Genome analysis of Elysia chlorotica Egg DNA provides no evidence for horizontal gene transfer into the germ line of this Kleptoplastic Mollusc". Molecular Biology and Evolution. 30 (8): 1843–52. doi:10.1093/molbev/mst084. PMC 3708498. PMID 23645554.
  109. ^ Xia, Jixing; Guo, Zhaojiang; Yang, Zezhong; Han, Haolin; Wang, Shaoli; Xu, Haifeng; Yang, Xin; Yang, Fengshan; Wu, Qingjun; Xie, Wen; Zhou, Xuguo; Dermauw, Wannes; Turlings, Ted C.J.; Zhang, Youjun (2021-04-01). "Whitefly hijacks a plant detoxification gene that neutralizes plant toxins" (PDF). Cell. 184 (7): 1693–1705.e17. doi:10.1016/j.cell.2021.02.014. PMID 33770502. S2CID 232359463.
  110. ^ Jaramillo, V. D. A., Vargas, W. A., Sukno, S. A., & Thon, M. R. (2013). New insights into the evolution and structure of Colletotrichum plant-like subtilisins (CPLSs). Communicative & Integrative Biology, 6(6), e59078.
  111. ^ a b Nikolaidis, N., Doran, N., & Cosgrove, D. J. (2014). Plant expansins in bacteria and fungi: evolution by horizontal gene transfer and independent domain fusion. Molecular biology and evolution, 31(2), 376-386.
  112. ^ a b Moran NA, Jarvik T (April 2010). "Lateral transfer of genes from fungi underlies carotenoid production in aphids". Science. 328 (5978): 624–7. Bibcode:2010Sci...328..624M. doi:10.1126/science.1187113. PMID 20431015. S2CID 14785276.
  113. ^ Fukatsu T (April 2010). "Evolution. A fungal past to insect color". Science. 328 (5978): 574–5. Bibcode:2010Sci...328..574F. doi:10.1126/science.1190417. PMID 20431000. S2CID 23686682.
  114. ^ Luo H, Hallen-Adams HE, Lüli Y, Sgambelluri RM, Li X, Smith M, et al. (May 2022). "Genes and evolutionary fates of the amanitin biosynthesis pathway in poisonous mushrooms". Proceedings of the National Academy of Sciences of the United States of America. 119 (20): e2201113119. Bibcode:2022PNAS..11901113L. doi:10.1073/pnas.2201113119. PMC 9171917. PMID 35533275. S2CID 248668772.
  115. ^ Wilcox C (2021-06-09). "DNA Jumps Between Animal Species. No One Knows How Often". Quanta Magazine. Retrieved 2021-06-15.
  116. ^ Martin JP, Fridovich I (June 1981). "Evidence for a natural gene transfer from the ponyfish to its bioluminescent bacterial symbiont Photobacter leiognathi. The close relationship between bacteriocuprein and the copper-zinc superoxide dismutase of teleost fishes". The Journal of Biological Chemistry. 256 (12): 6080–6089. doi:10.1016/S0021-9258(19)69131-3. PMID 6787049.
  117. ^ Bar D (16 February 2011). "Evidence of Massive Horizontal Gene Transfer Between Humans and Plasmodium vivax". Nature Precedings. doi:10.1038/npre.2011.5690.1.
  118. ^ "Human beings' ancestors have routinely stolen genes from other species". The Economist. 14 March 2015. Retrieved 17 March 2015.
  119. ^ Salzberg SL, White O, Peterson J, Eisen JA (June 2001). "Microbial genes in the human genome: lateral transfer or gene loss?". Science. 292 (5523): 1903–6. Bibcode:2001Sci...292.1903S. doi:10.1126/science.1061036. PMID 11358996. S2CID 17016011.
  120. ^ Andersson DI, Hughes D (July 2014). "Microbiological effects of sublethal levels of antibiotics". Nature Reviews. Microbiology. 12 (7): 465–478. doi:10.1038/nrmicro3270. PMID 24861036. S2CID 3351736.
  121. ^ a b c d e Wang Y, Lu J, Zhang S, Li J, Mao L, Yuan Z, et al. (September 2021). "Non-antibiotic pharmaceuticals promote the transmission of multidrug resistance plasmids through intra- and intergenera conjugation". The ISME Journal. 15 (9): 2493–2508. doi:10.1038/s41396-021-00945-7. PMC 8397710. PMID 33692486.
  122. ^ a b c d e f g Jiao YN, Chen H, Gao RX, Zhu YG, Rensing C (October 2017). "Organic compounds stimulate horizontal transfer of antibiotic resistance genes in mixed wastewater treatment systems". Chemosphere. 184: 53–61. Bibcode:2017Chmsp.184...53J. doi:10.1016/j.chemosphere.2017.05.149. PMID 28578196.
  123. ^ a b c d e f g h Ma X, Zhang X, Xia J, Sun H, Zhang X, Ye L (December 2021). "Phenolic compounds promote the horizontal transfer of antibiotic resistance genes in activated sludge". The Science of the Total Environment. 800: 149549. Bibcode:2021ScTEn.800n9549M. doi:10.1016/j.scitotenv.2021.149549. PMID 34392203.
  124. ^ a b c d e f Zhang Y, Gu AZ, Cen T, Li X, He M, Li D, Chen J (June 2018). "Sub-inhibitory concentrations of heavy metals facilitate the horizontal transfer of plasmid-mediated antibiotic resistance genes in water environment". Environmental Pollution. 237: 74–82. doi:10.1016/j.envpol.2018.01.032. PMID 29477117. S2CID 4911120.
  125. ^ Ivics Z, Hackett PB, Plasterk RH, Izsvák Z (November 1997). "Molecular reconstruction of Sleeping Beauty, a Tc1-like transposon from fish, and its transposition in human cells". Cell. 91 (4): 501–510. doi:10.1016/S0092-8674(00)80436-5. PMID 9390559. S2CID 17908472.
  126. ^ Plasterk RH (1996). "The Tc1/mariner transposon family". In Saedler H, Gierl A (eds.). Transposable Elements. Current Topics in Microbiology and Immunology. Vol. 204. pp. 125–143. doi:10.1007/978-3-642-79795-8_6. ISBN 978-3-642-79797-2. PMID 8556864.
  127. ^ Izsvák Z, Ivics Z, Plasterk RH (September 2000). "Sleeping Beauty, a wide host-range transposon vector for genetic transformation in vertebrates". Journal of Molecular Biology. 302 (1): 93–102. doi:10.1006/jmbi.2000.4047. PMID 10964563.
  128. ^ Kurtti TJ, Mattila JT, Herron MJ, Felsheim RF, Baldridge GD, Burkhardt NY, et al. (October 2008). "Transgene expression and silencing in a tick cell line: A model system for functional tick genomics". Insect Biochemistry and Molecular Biology. 38 (10): 963–968. doi:10.1016/j.ibmb.2008.07.008. PMC 2581827. PMID 18722527.
  129. ^ Graham Lawton Why Darwin was wrong about the tree of life New Scientist Magazine issue 2692 21 January 2009 Accessed February 2009
  130. ^ Badger JH, Eisen JA, Ward NL (May 2005). "Genomic analysis of Hyphomonas neptunium contradicts 16S rRNA gene-based phylogenetic analysis: implications for the taxonomy of the orders 'Rhodobacterales' and Caulobacterales". International Journal of Systematic and Evolutionary Microbiology. 55 (Pt 3): 1021–1026. doi:10.1099/ijs.0.63510-0. PMID 15879228.
  131. ^ Zhaxybayeva O, Gogarten JP (April 2004). "Cladogenesis, coalescence and the evolution of the three domains of life". Trends in Genetics. 20 (4): 182–7. doi:10.1016/j.tig.2004.02.004. PMID 15041172.
  132. ^ a b c Doolittle WF (February 2000). "Uprooting the tree of life". Scientific American. 282 (2): 90–5. Bibcode:2000SciAm.282b..90D. doi:10.1038/scientificamerican0200-90. PMID 10710791.
  133. ^ Woese CR (June 2004). "A new biology for a new century". Microbiology and Molecular Biology Reviews. 68 (2): 173–86. doi:10.1128/MMBR.68.2.173-186.2004. PMC 419918. PMID 15187180.
  134. ^ Theobald DL (May 2010). "A formal test of the theory of universal common ancestry". Nature. 465 (7295): 219–22. Bibcode:2010Natur.465..219T. doi:10.1038/nature09014. PMID 20463738. S2CID 4422345.
  135. ^ Huang J, Gogarten JP (2009). "Ancient gene transfer as a tool in phylogenetic reconstruction". Horizontal Gene Transfer. Methods in Molecular Biology. Vol. 532. Humana Press. pp. 127–39. doi:10.1007/978-1-60327-853-9_7. ISBN 9781603278522. PMID 19271182.
  136. ^ Davín AA, Tannier E, Williams TA, Boussau B, Daubin V, Szöllősi GJ (May 2018). "Gene transfers can date the tree of life". Nature Ecology & Evolution. 2 (5): 904–909. doi:10.1038/s41559-018-0525-3. PMC 5912509. PMID 29610471.
  137. ^ Wolfe JM, Fournier GP (May 2018). "Horizontal gene transfer constrains the timing of methanogen evolution". Nature Ecology & Evolution. 2 (5): 897–903. doi:10.1038/s41559-018-0513-7. hdl:1721.1/118329. PMID 29610466. S2CID 4968981.
  138. ^ Oliveira PH, Touchon M, Cury J, Rocha EP (October 2017). "The chromosomal organization of horizontal gene transfer in bacteria". Nature Communications. 8 (1): 841. Bibcode:2017NatCo...8..841O. doi:10.1038/s41467-017-00808-w. PMC 5635113. PMID 29018197.
  139. ^ Bryant DA, Frigaard NU (November 2006). "Prokaryotic photosynthesis and phototrophy illuminated". Trends in Microbiology. 14 (11): 488–96. doi:10.1016/j.tim.2006.09.001. PMID 16997562.
  140. ^ Avrain L, Vernozy-Rozand C, Kempf I (2004). "Evidence for natural horizontal transfer of tetO gene between Campylobacter jejuni strains in chickens". Journal of Applied Microbiology. 97 (1): 134–40. doi:10.1111/j.1365-2672.2004.02306.x. PMID 15186450. S2CID 19184139.
  141. ^ Darkened Forests, Ferns Stole Gene From an Unlikely Source — and Then From Each Other Archived 2016-03-07 at the Wayback Machine by Jennifer Frazer (May 6, 2014). Scientific American.
  142. ^ Li FW, Rothfels CJ, Melkonian M, Villarreal JC, Stevenson DW, Graham SW, et al. (2015). "The origin and evolution of phototropins". Frontiers in Plant Science. 6: 637. doi:10.3389/fpls.2015.00637. PMC 4532919. PMID 26322073.
  143. ^ Wybouw N, Dermauw W, Tirry L, Stevens C, Grbić M, Feyereisen R, Van Leeuwen T (April 2014). "A gene horizontally transferred from bacteria protects arthropods from host plant cyanide poisoning". eLife. 3: e02365. doi:10.7554/eLife.02365. PMC 4011162. PMID 24843024.
  144. ^ Yong E (2011-02-16). "Gonorrhea has picked up human DNA (and that's just the beginning)". National Geographic. Retrieved 2016-07-14.
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