In evolutionary genetics, Muller's ratchet (named after Hermann Joseph Muller, by analogy with a ratchet effect) is a process by which the genomes of an asexual population accumulate deleterious mutations (harmful mutations) in an irreversible manner. Muller proposed this mechanism as one reason why sexual reproduction may be favored over asexual reproduction. 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.
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, and the phrase "Muller's ratchet" was coined by Joe Felsenstein in his 1974 paper, "The Evolutionary Advantage of Recombination".
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. 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]). 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.
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) 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. However, some asexual lineages are thought to be quite ancient; Bdelloid rotifers, for example, appear to have been asexual for nearly 40 million years. However, rotifers were found to possess a substantial number of foreign genes from possible horizontal gene transfer events.
It has been argued that recombination was an evolutionary development as ancient as life itself. Early RNA replicators capable of recombination may have been the ancestral sexual source from which asexual lineages could periodically emerge. Recombination in the early sexual lineages may have provided a means for coping with genome damage. Muller's ratchet under such ancient conditions would likely have impeded the evolutionary persistence of the asexual lineages that were unable to undergo recombination.