Jump to content

DNA transposon

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Monkbot (talk | contribs) at 23:55, 6 December 2020 (Task 18 (cosmetic): eval 34 templates: del empty params (3×); cvt lang vals (1×);). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

DNA transposons are DNA sequences, sometimes referred to "jumping genes", that can move and integrate to different locations within the genome.[1] 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.[2] DNA transposons can move in the DNA of an organism via a single-or double-stranded DNA intermediate.[3] 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.[4] It is important to note that DNA transposons do not randomly insert themselves into the genome, but rather show preference for specific sites.

With regard to movement, DNA transposons can be categorized as autonomous and nonautonomous.[5] Autonomous ones can move on their own, while nonautonomous ones require the presence of another transposable element's gene, transposase, to move. There are three main classifications for movement for DNA transposons: "cut and paste,"[6] "rolling circle" (Helitrons),[7] and "self-synthesizing" (Polintons).[8] These distinct mechanisms of movement allow them to move around the genome of an organism. Since DNA transposons cannot synthesize DNA, they replicate using the host replication machinery. These three main classes are then further broken down into 23 different superfamilies characterized by their structure, sequence, and mechanism of action.[9]

DNA transposons are a cause of gene expression alterations. As newly inserted DNA into active coding sequences, they can disrupt normal protein functions and cause mutations. Class II TEs make up about 3% of the human genome. Today, there are no active DNA transposons in the human genome. Therefore, the elements found in the human genome are called fossils.

Mechanisms of action

Cut and paste

"Cut and Paste" transposable element mechanism of excision and insertion into target site.

Traditionally, DNA transposons move around in the genome by a cut and paste method. The system requires a transposase enzyme that catalyzes the movement of the DNA from its current location in the genome and inserts it in a new location. Transposition requires three DNA sites on the transposon: two at each end of the transposon called terminal inverted repeats and one at the target site. The transposase will bind to the terminal inverted repeats of the transposon and mediate synapsis of the transposon ends. The transposase enzyme then disconnects the element from the flanking DNA of the original donor site and mediates the joining reaction that links the transposon to the new insertion site. The addition of the new DNA into the target site causes short gaps on either side of the inserted segment.[10] Host systems repair these gaps resulting in the target sequence duplication (TSD) that are characteristic of transposition. In many reactions, the transposon is completely excised from the donor site in what is called a "cut and paste"[11] transposition and inserted into the target DNA to form a simple insertion. Occasionally, genetic material not originally in the transposable element gets copied and moved as well.

Helitrons

Rolling circle replication of a circular DNA plasmid.

Helitrons are also a group of eukaryotic class II TEs. Helitrons do not follow the classical "cut and paste" mechanism. Instead, they are hypothesized to move around the genome via a rolling circle like mechanism. This process involves making a nick to a circular strand by an enzyme, which separates the DNA into two single strands. The initiation protein then remains attached to the 5' Phosphate on the nicked strand, exposing the 3' hydroxyl of the complementary strand. This allows a polymerase enzyme to begin replication on the un-nicked strand. Eventually the entire strand is replicated at which point the newly synthesized DNA disassociates and is replicated in parallel with the original template strand.[12] Helitrons encode an unknown protein which is thought to have HUH endonuclease function as well as 5' to 3' helicase activity. This enzyme would make a single stranded cut in the DNA which explains the lack of Target Site Duplications found in Helitrons. Helitrons were also the first class of transposable elements to be discovered computationally and marked a paradigm shift in the way that whole genomes were studied.[13]

Polintons

Self-synthesizing transposition mechanism for Polintons.

Polintons are also a group of eukaryotic class II TEs. As one of the most complex known DNA transposons in eurkaryotes, they make up the genomes of protists, fungi, and animals, such as the entamoeba, soybean rust, and chicken, respectively. They contain genes with homology to viral proteins and which are often found in eukaryotic genomes, like polymerase and retroviral integrase. However, there is no known protein functionally similarly to the viral capsid or envelope proteins. They share their many structural characteristics with linear plasmids, bacteriophages and adenoviruses, which replicate using protein-primed DNA polymerases. Polintons have been proposed to go through a similar self-synthesis by their polymerase. Polintons, 15–20 kb long, encode up to 10 individual proteins. For replication, they utilize a protein-primed DNA polymerase B, retroviral integrase, cysteine protease, and ATPase. First, during host genome replication, a single-stranded extra-chromosomal Polinton element is excised from the host DNA using the integrase, forming a racket-like structure. Second, the Polinton undergoes replication using the DNA polymerase B, with initiation started by a terminal protein, which may encoded in some linear plasmids. Once the double stranded Polinton is generated, the integrase serves to insert it into the host genome. Polintons exhibit high variability between difference species and may tightly regulated, resulting in a low frequency rate in many genomes.[14]

Classification

As of the most recent update in 2015, 23 superfamilies of DNA transposons were recognized and annotated in Repbase, a database of repetitive DNA elements maintained by the Genetic Information Research Institute:[15]

Effects of transposons

Spotting on maize kernels shows activation of DNA transposons.

DNA transposons, like all transposons, are quite impactful with respect to gene expression. A sequence of DNA may insert itself into a previously functional gene and create a mutation. This can happen in three distinct ways: 1. alteration of function, 2. chromosomal rearrangement, and 3. a source of novel genetic material.[16] Since DNA transposons may happen to take parts of genomic sequences with them, exon shuffling may occur. Exon shuffling is the creation of novel gene products due to the new placement of two previously unrelated exons through transposition.[17] Because of their ability to alter DNA expression, transposons have become an important target of research in genetic engineering.

Barbara McClintock was the first to discover the existence of DNA transposons in maize plants at Cold Spring Harbor Laboratory. She was awarded the Nobel Prize in Physiology or Medicine in 1983.

Examples

Maize

Barbara McClintock first discovered and described DNA transposons in Zea mays,[18] during the 1940s; this is an achievement that would earn her the Nobel Prize in 1983. She described the Ac/Ds system where the Ac unit (activator) was autonomous but the Ds genomic unit required the presence of the activator in order to move. This TE is one of the most visually obvious as it was able to cause the maize to change color from yellow to brown/spotted on individual kernels.

Fruit flies

The Mariner/Tc1 transposon, found in many animals but studied in Drosophila was first described by Jacobson and Hartl.[19] Mariner is well known for being able to excise and insert horizontally in to a new organism.[20] Thousands of copies of the TE have been found interspersed in the human genome as well as other animals.

The Hobo transposons in Drosophila have been extensively studied due to their ability to cause gonadal dysgenesis.[21] The insertion and subsequent expression of hobo-like sequences results in the loss of germ cells in the gonads of developing flies.

Bacteria

Bacterial transposons are especially good at facilitating horizontal gene transfer between microbes. Transposition facilitates the transfer and accumulation of antibiotic resistance genes. In bacteria, transposable elements can easily jump between the chromosomal genome and plasmids. In a 1982 study by Devaud et al., a multi-drug resistant strain of Acinetobacter was isolated and examined. Evidence pointed to the transfer of a plasmid in to the bacterium, where the resistance genes were transposed in to the chromosomal genome.[22]

Genetic diversity

Transposons may have an effect on the promotion of genetic diversity of many organisms. DNA transposons can drive the evolution of genomes by promoting the relocation of sections of DNA sequences. As a result, this can alter gene regulatory regions and phenotypes.[23] The discovery of transposons was made by Barbara McClintock who noticed that these elements could actually change the color of the maize plants she was studying, providing quick evidence of one outcome from transposon movement.[24] Another example is the Tol2 DNA transposon in medaka fish that is said to be the result of their variety in pigmentation patterns.[25] These examples show that transposons can greatly influence the process of evolution by rapidly inducing changes in the genome.

Inactivation

All DNA transposons are inactive in the human genome.[26] Inactivated, or silenced, transposons do not result in a phenotypic outcome and do not move around in the genome. Some are inactive because they have mutations that affect their ability to move between chromosomes, while others are capable of moving but remain inactive due to epigenetic defenses, like DNA methylation and chromatin remodeling. For example, chemical modifications of DNA can constrict certain areas of the genome such that transcription enzymes are unable to reach them. RNAi, specifically siRNA and miRNA silencing, is a naturally occurring mechanisms that, in addition to regulating eukaryotic gene expression, prevents transcription of DNA transposons. Another mode of inactivation is overproduction inhibition. When transposase exceeds a threshold concentration, transposon activity is decreased.[27] Since transposase can form inactive or less active monomers that will decrease transposition activity overall, a decrease in the production of transposase will also occur when large copies of those less active those elements increase in the host genome.

Horizontal transfer

Horizontal transfer refers to the movement of DNA information between cells of different organisms. Horizontal transfer can involve the movement of TEs from one organism into the genome of another. The insertion itself allows the TE to become an activated gene in the new host. Horizontal transfer is used by DNA transposons to prevent inactivation and complete loss of the transposon. This inactivation is termed vertical inactivation, meaning that the DNA transposon is inactive and remains as a fossil. This type of transfer is not the most common, but has been seen in the case of the wheat virulence protein ToxA, which was transferred between the different fungal pathogens Parastagonospora nodorum, Pyrenophora tritici-repentis, and Bipolaris sorokiniana.[28] Other examples include transfer between marine crustaceans, insects of different orders, and organisms of different phyla, such as humans and nematodes.[29]

Evolution

Eukaryotic genomes differ in TE content. Recently, a study of the different superfamilies of TEs reveals that there are striking similarities between the groups. It has been hypothesized that many of them are represented in two or more Eukaryotic supergroups. This means that divergence of the transposon superfamilies could even predate the divergence of Eukaryotic supergroups.[30]

V(D)J recombination

V(D)J recombination, although not a DNA TE, is remarkably similar to transposons. V(D)J recombination is the process by which the large variation in antibody binding sites is created. In this mechanism, DNA is recombined in order to create genetic diversity.[31] Because of this, it has been hypothesized that these proteins, particularly Rag1 and Rag2[32] are derived from transposable elements.[33]

Extinction in the human genome

There is evidence suggesting that at least 40 human DNA transposon families were active during mammalian radiation and early primate lineage. Then, there was a pause in transpositional activity during the later portion of primate radiation, with a complete halt in transposon movement in an anthropoid primate ancestor. There is no evidence of any transposable element younger than about 37 million years.[34]

References

  1. ^ "Transposon | genetics". Encyclopedia Britannica. Retrieved 2019-10-28.
  2. ^ Wicker, Thomas; Sabot, François; Hua-Van, Aurélie; Bennetzen, Jeffrey L.; Capy, Pierre; Chalhoub, Boulos; Flavell, Andrew; Leroy, Philippe; Morgante, Michele (2007). "A unified classification system for eukaryotic transposable elements". Nature Reviews Genetics. 8 (12): 973–982. doi:10.1038/nrg2165. PMID 17984973. S2CID 32132898.
  3. ^ Feschotte, Cédric; Pritham, Ellen J. (December 2007). "DNA Transposons and the Evolution of Eukaryotic Genomes". Annual Review of Genetics. 41 (1): 331–368. doi:10.1146/annurev.genet.40.110405.090448. PMC 2167627. PMID 18076328.
  4. ^ Muñoz-López, Martín; García-Pérez, José L. (April 2010). "DNA Transposons: Nature and Applications in Genomics". Current Genomics. 11 (2): 115–128. doi:10.2174/138920210790886871. ISSN 1389-2029. PMC 2874221. PMID 20885819.
  5. ^ "Transposons | Learn Science at Scitable". www.nature.com. Retrieved 2019-10-28.
  6. ^ Craig, Nancy L. (1995-10-13). "Unity in Transposition Reactions". Science. 270 (5234): 253–4. Bibcode:1995Sci...270..253C. doi:10.1126/science.270.5234.253. ISSN 0036-8075. PMID 7569973.
  7. ^ Kapitonov, Vladimir V.; Jurka, Jerzy (2001-07-17). "Rolling-circle transposons in eukaryotes". Proceedings of the National Academy of Sciences of the United States of America. 98 (15): 8714–8719. Bibcode:2001PNAS...98.8714K. doi:10.1073/pnas.151269298. ISSN 0027-8424. PMC 37501. PMID 11447285.
  8. ^ Kapitonov, Vladimir V.; Jurka, Jerzy (2006-03-21). "Self-synthesizing DNA transposons in eukaryotes". Proceedings of the National Academy of Sciences of the United States of America. 103 (12): 4540–4545. Bibcode:2006PNAS..103.4540K. doi:10.1073/pnas.0600833103. ISSN 0027-8424. PMC 1450207. PMID 16537396.
  9. ^ Kapitonov, Vladimir V.; Jurka, Jerzy (2006-03-21). "Self-synthesizing DNA transposons in eukaryotes". Proceedings of the National Academy of Sciences of the United States of America. 103 (12): 4540–4545. Bibcode:2006PNAS..103.4540K. doi:10.1073/pnas.0600833103. ISSN 0027-8424. PMC 1450207. PMID 16537396.
  10. ^ Berg and Howe, Douglas E. and Martha M. (1989). Mobile DNA II. ASM Press. p. 98. ISBN 9781555812096.
  11. ^ Madigan M, Martinko J, eds. (2006). Brock Biolog of Microorganisms (11th ed.). Prentice Hall. ISBN 0-13-144329-1.
  12. ^ "Rolling circle replication - The School of Biomedical Sciences Wiki". teaching.ncl.ac.uk. Retrieved 2019-10-06.
  13. ^ Thomas J, Pritham EJ (August 2015). "Helitrons, the Eukaryotic Rolling-circle Transposable Elements". Microbiology Spectrum. 3 (4): 893–926. doi:10.1128/microbiolspec.MDNA3-0049-2014. ISBN 9781555819200. PMID 26350323.
  14. ^ Kapitonov VV, Jurka J (March 2006). "Self-synthesizing DNA transposons in eukaryotes". Proceedings of the National Academy of Sciences of the United States of America. 103 (12): 4540–5. Bibcode:2006PNAS..103.4540K. doi:10.1073/pnas.0600833103. PMC 1450207. PMID 16537396.
  15. ^ Bao W, Kojima KK, Kohany O (2 June 2015). "Repbase Update, a database of repetitive elements in eukaryotic genomes". Mobile DNA. 6 (1): 11. doi:10.1186/s13100-015-0041-9. PMC 4455052. PMID 26045719.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  16. ^ Feschotte C, Pritham EJ (2007). "DNA transposons and the evolution of eukaryotic genomes". Annual Review of Genetics. 41: 331–68. doi:10.1146/annurev.genet.40.110405.090448. PMC 2167627. PMID 18076328.
  17. ^ Morgante M, Brunner S, Pea G, Fengler K, Zuccolo A, Rafalski A (September 2005). "Gene duplication and exon shuffling by helitron-like transposons generate intraspecies diversity in maize". Nature Genetics. 37 (9): 997–1002. doi:10.1038/ng1615. PMID 16056225. S2CID 10401931.
  18. ^ McClintock, Barbara (1950). "The origin and behavior of mutable loci in maize". Proc Natl Acad Sci U S A. 36 (6): 344–55. Bibcode:1950PNAS...36..344M. doi:10.1073/pnas.36.6.344. PMC 1063197. PMID 15430309.
  19. ^ Jacobson, JW; Medhora, MM; Hartl, DL (Nov 1986). "Molecular structure of a somatically unstable transposable element in Drosophila". Proc Natl Acad Sci U S A. 83 (22): 8684–8. Bibcode:1986PNAS...83.8684J. doi:10.1073/pnas.83.22.8684. PMC 386995. PMID 3022302.
  20. ^ Lohe, AR; Moriyama, EN; Lidholm, DA; Hartl, DL (1995). "Horizontal transmission, vertical inactivation, and stochastic loss of mariner-like transposable elements". Mol. Biol. Evol. 12 (1): 62–72. doi:10.1093/oxfordjournals.molbev.a040191. PMID 7877497.
  21. ^ Deprá, M; Valente, VL; Margis, R; Loreto, EL (2009). "The hobo transposon and hobo-related elements are expressed as developmental genes in Drosophila". Gene. 448 (1): 57–63. doi:10.1016/j.gene.2009.08.012. PMID 19720121.
  22. ^ Devaud, M; Kayser, FH; Bächi, B (Aug 1982). "Transposon-mediated multiple antibiotic resistance in Acinetobacter strains". Antimicrob Agents Chemother. 22 (2): 323–9. doi:10.1128/aac.22.2.323. PMC 183733. PMID 6100428.
  23. ^ "Transposons | Learn Science at Scitable". www.nature.com. Retrieved 2019-11-01.
  24. ^ "Barbara McClintock and the Discovery of Jumping Genes (Transposons) | Learn Science at Scitable". www.nature.com. Retrieved 2019-10-07.
  25. ^ Koga, Akihiko; Iida, Atsuo; Hori, Hiroshi; Shimada, Atsuko; Shima, Akihiro (July 2006). "Vertebrate DNA transposon as a natural mutator: the medaka fish Tol2 element contributes to genetic variation without recognizable traces". Molecular Biology and Evolution. 23 (7): 1414–1419. doi:10.1093/molbev/msl003. ISSN 0737-4038. PMID 16672286.
  26. ^ "Transposons | Learn Science at Scitable". www.nature.com. Retrieved 2019-11-01.
  27. ^ Muñoz-López, Martín; García-Pérez, José L. (April 2010). "DNA Transposons: Nature and Applications in Genomics". Current Genomics. 11 (2): 115–128. doi:10.2174/138920210790886871. ISSN 1389-2029. PMC 2874221. PMID 20885819.
  28. ^ McDonald, Megan C.; Taranto, Adam P.; Hill, Erin; Schwessinger, Benjamin; Liu, Zhaohui; Simpfendorfer, Steven; Milgate, Andrew; Solomon, Peter S. (2019-10-29). "Transposon-Mediated Horizontal Transfer of the Host-Specific Virulence Protein ToxA between Three Fungal Wheat Pathogens". mBio. 10 (5). doi:10.1128/mBio.01515-19. ISSN 2150-7511. PMC 6737239. PMID 31506307.
  29. ^ Muñoz-López, Martín; García-Pérez, José L. (April 2010). "DNA Transposons: Nature and Applications in Genomics". Current Genomics. 11 (2): 115–128. doi:10.2174/138920210790886871. ISSN 1389-2029. PMC 2874221. PMID 20885819.
  30. ^ Feschotte C, Pritham EJ (2007). "DNA transposons and the evolution of eukaryotic genomes". Annual Review of Genetics. 41: 331–68. doi:10.1146/annurev.genet.40.110405.090448. PMC 2167627. PMID 18076328.
  31. ^ Jung D, Alt FW (January 2004). "Unraveling V(D)J recombination; insights into gene regulation". Cell. 116 (2): 299–311. doi:10.1016/S0092-8674(04)00039-X. PMID 14744439. S2CID 16890458.
  32. ^ Bourque G, Burns KH, Gehring M, Gorbunova V, Seluanov A, Hammell M, et al. (November 2018). "Ten things you should know about transposable elements". Genome Biology. 19 (1): 199. doi:10.1186/s13059-018-1577-z. PMC 6240941. PMID 30454069.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  33. ^ Muñoz-López M, García-Pérez JL (April 2010). "DNA transposons: nature and applications in genomics". Current Genomics. 11 (2): 115–28. doi:10.2174/138920210790886871. PMC 2874221. PMID 20885819.
  34. ^ Pace JK, Feschotte C (April 2007). "The evolutionary history of human DNA transposons: evidence for intense activity in the primate lineage". Genome Research. 17 (4): 422–32. doi:10.1101/gr.5826307. PMC 1832089. PMID 17339369.
Retrieved from "https://en.wikipedia.org/w/index.php?title=DNA_transposon&oldid=992765460"