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Illustration of chromosome crossover during genetic recombination

In evolutionary genetics, Muller's ratchet (named after Hermann Joseph Muller, by analogy with a ratchet effect) is a process in which absence of recombination, especially in asexual population, results in accumulation of deleterious mutations (harmful mutations) in an irreversible manner.[1][2] This happens due to the fact that in absence of recombination, offspring cannot contain less mutations than their parents (assuming reverse mutations are rare)[2]. Muller proposed this mechanism as one reason why sexual reproduction may be favored over asexual reproduction, as sexual organism can benefit from recombination. He proposed that selection, to some extent, decreases the mutational load when recombination allows for different combination of mutations[2]. The negative effect of accumulating irreversible deleterious mutations may not be prevalent in organisms, which, while they reproduce asexually, also undergo other forms of recombination. This effect has also been observed in those regions of the genomes of sexual organisms that do not undergo recombination.



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] Also, laboratory experiments have confirmed the existence of ratchet and the consequent extinction of populations in many organisms (under intense drift and when recombinations are not allowed) including RNA viruses, bacteria, and eukaryotes[6][7][8]. In sexual populations, the process of genetic recombination allows the genomes of the offspring to be different from the genomes of the parents. In particular, progeny (offspring) genomes with fewer mutations can be generated from more highly mutated parental genomes by putting together mutation-free portions of parental chromosomes.

Among protists and prokaryotes, a plethora of supposedly asexual organisms exists. 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]).[9] 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.[10]

In sexually reproducing organisms, nonrecombining chromosomes or chromosomal regions such as the mammalian Y chromosome (with the exception of multicopy sequences which do engage intrachromosomal recombination and gene conversion[5]) should also be subject to the effects of Muller's ratchet. Such nonrecombining 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. Ascribing cases of genome shrinkage or fast evolution to Muller's ratchet alone is not easy.

Because Muller's ratchet relies on genetic drift, it turns faster in smaller populations and is thought to set limits to the maximum size of asexual genomes and to the long-term evolutionary continuity of asexual lineages.[11] However, some asexual lineages are thought to be quite ancient; Bdelloid rotifers, for example, appear to have been asexual for nearly 40 million years.[12] However, rotifers were found to possess a substantial number of foreign genes from possible horizontal gene transfer events.[13]


The antiquity of recombination and Muller's ratchet

It has been argued that recombination was an evolutionary development as ancient as life itself.[14] Early RNA replicators capable of recombination may have been the ancestral sexual source from which asexual lineages could periodically emerge.[14] Recombination in the early sexual lineages may have provided a means for coping with genome damage.[15] Muller's ratchet under such ancient conditions would likely have impeded the evolutionary persistence of the asexual lineages that were unable to undergo recombination.[14]

Calculation of the fittest class edit

In 1978 John Haigh used a Wright-Fisher model to analyze the effect of Muller's ratchet in an asexual population.[16] If the ratchet is operating the fittest class (least loaded individulas) is small and prone to extinction by the effect of genetic drift. In his paper Haigh drives the equation that calculates the frequency of individuals carrying   mutations for the population with stationary distribution:

 

 

where,   is the number of individual carrying   mutations,   is the population size,   is the mutation rate and   is the selection coefficient.

Thus, the frequency of the individuals of the fittest class ( ) is:


 


In an asexual population that suffers from ratchet the frequency of fittest individuals would be small, and would go extinct after few generations[16]. This increase the rate of accumulation of deleterious mutation, which ultimately results in the extinction of the population.

The antiquity of recombination and Muller's ratchet edit

It has been argued that recombination was an evolutionary development as ancient as life itself.[14] Early RNA replicators capable of recombination may have been the ancestral sexual source from which asexual lineages could periodically emerge.[14] Recombination in the early sexual lineages may have provided a means for coping with genome damage.[15] Muller's ratchet under such ancient conditions would likely have impeded the evolutionary persistence of the asexual lineages that were unable to undergo recombination.[14]

Muller's ratchet and mutational meltdown edit

Since deleterious mutations are harmful by definition, accumulation of them would result in loss of individuals and a smaller population size. Small populations are more susceptible to the ratchet effect and more deleterious mutations would be fixed as a result of genetic drift. This creates a positive feed-back loop that accelerate the extinction of small asexual populations. This phenomenon has been called mutational meltdown.[17]


Also in vertebrates, Poecilia formosa, seem to defy the ratchet effect (has existed for 500,000 generations). This has been explained by maintenance of genomic diversity through parental introgression and a high level of heterozygosity resulting from the hybrid origin of this species.[18]

See also edit

References edit

  1. ^ Muller HJ (1932). "Some genetic aspects of sex". American Naturalist. 66 (703): 118–138. doi:10.1086/280418. (Muller's original 1932 paper)
  2. ^ a b c 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. {{cite book}}: |edition= has extra text (help))
  3. ^ Muller HJ (1964). "The relation of recombination to mutational advance". Mutat Res. 106: 2–9. PMID 14195748.
  4. ^ Felsenstein J (1974). "The evolutionary advantage of recombination". Genetics. 78 (2): 737–756. PMC 1213231. PMID 4448362.
  5. ^ a b Freeman, Scott; Herron, Jon C (2007). Evolutionary Analysis, 4th edition. San Francisco: Benjamin Cummings. pp. 308–309. ISBN 0-13-227584-8.
  6. ^ Chao, Lin (November 1990). "Fitness of RNA virus decreased by Muller's ratchet". Nature. 348: 454–455.
  7. ^ Andersson, D. I.; Hughes, D. (1996-01-23). "Muller's ratchet decreases fitness of a DNA-based microbe". Proceedings of the National Academy of Sciences. 93 (2): 906–907. doi:10.1073/pnas.93.2.906. ISSN 0027-8424. PMC 40156. PMID 8570657.{{cite journal}}: CS1 maint: PMC format (link)
  8. ^ Zeyl, Clifford; Mizesko, Melissa; Visser, J. Arjan G. M. de (2001). "MUTATIONAL MELTDOWN IN LABORATORY YEAST POPULATIONS". Evolution. 55 (5): 909. doi:10.1554/0014-3820(2001)055[0909:MMILYP]2.0.CO;2. ISSN 0014-3820.
  9. ^ 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.
  10. ^ 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.)
  11. ^ Freeman, Scott; Herron, Jon C (2007). Evolutionary Analysis, 4th edition. San Francisco: Benjamin Cummings. p. 309. ISBN 0-13-227584-8.
  12. ^ "Bdelloids: No sex for over 40 million years". TheFreeLibrary. ScienceNews. Retrieved 30 April 2011.
  13. ^ 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. PMC 3499245.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  14. ^ a b c d e f Lehman N (June 2003). "A case for the extreme antiquity of recombination". J. Mol. Evol. 56 (6): 770–7. doi:10.1007/s00239-003-2454-1. PMID 12911039.
  15. ^ a b Bernstein H, Byerly HC, Hopf FA, Michod RE (October 1984). "Origin of sex". J. Theor. Biol. 110 (3): 323–51. doi:10.1016/s0022-5193(84)80178-2. PMID 6209512.
  16. ^ a b Haigh, John (1978-10-01). "The accumulation of deleterious genes in a population—Muller's Ratchet". Theoretical Population Biology. 14 (2): 251–267. doi:10.1016/0040-5809(78)90027-8. ISSN 0040-5809.
  17. ^ Gabriel, W.; Lynch, M.; Bürger, R. (1993). "Muller's Ratchet and Mutational Meltdowns". Evolution. 47 (6): 1744–1757. doi:10.1111/j.1558-5646.1993.tb01266.x. ISSN 1558-5646.
  18. ^ Warren, Wesley C.; García-Pérez, Raquel; Xu, Sen; Lampert, Kathrin P.; Chalopin, Domitille; Stöck, Matthias; Loewe, Laurence; Lu, Yuan; Kuderna, Lukas; Minx, Patrick; Montague, Michael J. (2018-02-12). "Clonal polymorphism and high heterozygosity in the celibate genome of the Amazon molly". Nature Ecology & Evolution. 2 (4): 669–679. doi:10.1038/s41559-018-0473-y. ISSN 2397-334X.


Category:Population genetics Category:Evolutionary biology

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