Contents 1 Origin of the term 2 Explanation 3 See also 4 References

Origin of the term[edit] Although Muller discussed the advantages of sexual reproduction in his 1932 talk, it does not contain the word "ratchet". Muller first introduced the term "ratchet" in his 1964 paper,[3] and the phrase "Muller's ratchet" was coined by Joe Felsenstein in his 1974 paper, "The Evolutionary Advantage of Recombination".[4]

Explanation[edit] Asexual reproduction compels genomes to be inherited as indivisible blocks so that once the least mutated genomes in an asexual population begin to carry at least one deleterious mutation, no genomes with fewer such mutations can be expected to be found in future generations (except as a result of back mutation). This results in an eventual accumulation of mutations known as genetic load. In theory, the genetic load carried by asexual populations eventually becomes so great that the population goes extinct.[5] In sexual populations, the process of genetic recombination allows the genomes of the progeny to be different from the genomes of the parents. In particular, progeny genomes with fewer mutations can be generated from more highly mutated parental genomes by putting together in progeny genomes mutation-free portions of parental chromosomes. Among protists and prokaryotes there is a plethora of supposedly asexual organisms. More and more are being shown to exchange genetic information through a variety of mechanisms. In contrast, the genomes of mitochondria and chloroplasts do not recombine and would undergo Muller's ratchet were they not as small as they are (see Birdsell and Wills [pp. 93–95]).[6] Indeed, the probability that the least mutated genomes in an asexual population end up carrying at least one (additional) mutation depends heavily on the genomic mutation rate and this increases more or less linearly with the size of the genome (more accurately, with the number of base pairs present in active genes). However, reductions in genome size, especially in parasites and symbionts, can also be caused by direct selection to get rid of genes that have become unnecessary. Therefore, a smaller genome is not a sure indication of the action of Muller's ratchet.[7] In sexually reproducing organisms, non-recombining chromosomes or chromosomal regions such as the mammalian Y chromosome (with the exception of multi-copy sequences which do engage intrachromosomal recombination and gene conversion[5]) should also be subject to the effects of Muller's ratchet. Such non-recombining sequences tend to shrink and evolve quickly. However this fast evolution might also be due to these sequences' inability to repair DNA damage via template-assisted repair which is equivalent to an increase in the mutation rate for these sequences. It is not easy to ascribe cases of genome shrinkage or fast evolution to Muller's ratchet alone. Because Muller's ratchet relies on genetic drift, it turns faster in smaller populations and it is thought to set limits to the maximum size of asexual genomes and to the long-term evolutionary continuity of asexual lineages.[8] However, some asexual lineages are thought to be quite ancient: Bdelloid rotifers, for example, appear to have been asexual for nearly 40 million years.[9] However, rotifers were found to possess a substantial amount of foreign genes from possible horizontal gene transfer events.[10]

See also[edit] Evolution of sexual reproduction Genetic hitchhiking Mutational meltdown Hill-Robertson effect

References[edit] ^ Muller HJ (1932). "Some genetic aspects of sex". American Naturalist. 66 (703): 118–138. doi:10.1086/280418.  (Muller's original 1932 paper) ^ Muller HJ (1964). "The relation of recombination to mutational advance". Mutat Res. 106: 2–9. PMID 14195748.  (original paper as cited by, e.g.: Maynard Smith J; Szathmary E (1997). The major transitions in evolution. Oxford, New York, Tokyo: Oxford University Press.  ; Futuyma DJ (1998). Evolutionary biology (3rd edn ed.). Sunderland, Mass.: Sinauer Associates. ) ^ Muller HJ (1964). "The relation of recombination to mutational advance". Mutat Res. 106: 2–9. PMID 14195748.  ^ Felsenstein J (1974). "The evolutionary advantage of recombination". Genetics. 78 (2): 737–756. PMC 1213231 . PMID 4448362.  ^ a b Freeman, Scott; Herron, Jon C (2007). Evolutionary Analysis, 4th edition. San Francisco: Benjamin Cummings. pp. 308–309. ISBN 0-13-227584-8.  ^ Birdsell JA, Wills C (2003). The evolutionary origin and maintenance of sexual recombination: A review of contemporary models. Evolutionary Biology Series >> Evolutionary Biology, Vol. 33 pp. 27-137. MacIntyre, Ross J.; Clegg, Michael, T (Eds.), Springer. Hardcover ISBN 978-0306472619, ISBN 0306472619 Softcover ISBN 978-1-4419-3385-0. ^ Nancy A. Moran (April 1996). "Accelerated evolution and Muller's ratchet in endosymbiotic bacteria". Proceedings of the National Academy of Sciences USA. 93 (7): 2873–2878. doi:10.1073/pnas.93.7.2873. PMC 39726 . PMID 8610134.  (An article that discusses Muller's ratchet in the context of endosymbiotic bacteria.) ^ Freeman, Scott; Herron, Jon C (2007). Evolutionary Analysis, 4th edition. San Francisco: Benjamin Cummings. p. 309. ISBN 0-13-227584-8.  ^ "Bdelloids: No sex for over 40 million years". TheFreeLibrary. ScienceNews. Retrieved 30 April 2011.  ^ Chiara Boschetti; Adrian Carr; Alastair Cris (November 15, 2012). "Biochemical Diversification through Foreign Gene Expression in Bdelloid Rotifers". PLOS Genetics. doi:10.1371/journal.pgen.1003035.  v t e Extinction Phenomena Background extinction rate Coextinction De-extinction Ecological extinction Extinct in the wild Functional extinction Genetic pollution Lazarus taxon Local extinction Pseudoextinction Models Extinction vortex Causes Genetic erosion Habitat destruction Human overpopulation Muller's ratchet Mutational meltdown Overexploitation Theories & concepts Extinction debt Extinction risk from global warming Extinction threshold Field of Bullets Hypothetical species Latent extinction risk Major extinction events Ordovician–Silurian Late Devonian Permian–Triassic Triassic–Jurassic Cretaceous–Paleogene Holocene Timeline Other extinction events Great Oxygenation End-Ediacaran End-Botomian Dresbachian Cambrian–Ordovician Ireviken Mulde Lau Carboniferous Olson's End-Capitanian Carnian Pluvial Toarcian End-Jurassic or Tithonian Aptian Cenomanian-Turonian Eocene–Oligocene Middle Miocene Pliocene–Pleistocene Quaternary Extinct species Lists of extinct species Lists of extinct animals List of extinct plants IUCN Red List extinct species Organizations International Union for Conservation of Nature IUCN Species Survival Commission Voluntary Human Extinction Movement See also Decline in amphibian populations Human extinction Category     Portal     WikiProject     Commons Retrieved from "" Categories: Population geneticsEvolutionary biology

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