Evolutionary consequences of DNA mismatch inhibited repair opportunity.
Author(s) -
Wolfgang Stephan,
Charles H. Langley
Publication year - 1992
Publication title -
genetics.
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
ISSN - 3049-7094
DOI - 10.1093/genetics/132.2.567
Subject(s) - loss of heterozygosity , biology , genetics , homologous recombination , dna , recombination , dna repair , population , natural selection , molecular evolution , negative selection , homologous chromosome , dna mismatch repair , selection (genetic algorithm) , evolutionary biology , allele , gene , genome , demography , sociology , artificial intelligence , computer science
Double strand breaks (DSBs) are often repaired via homologous recombination. Recombinational repair processes are expected to be influenced by nucleotide heterozygosity through mismatch detection systems. Unrepaired DSBs have severe biological consequences and are often lethal. We show that natural selection due to inhibition of recombinational repair associated with polymorphisms could influence their molecular evolution. The main conclusions from this analysis are that, for increasing population size, mismatch detection leads to a limit on average heterozygosity of otherwise selectively neutral polymorphism, an excess of rare variants, and a slowing down of the rate of neutral molecular evolution. The first two results suggest that mismatch detection may account for the surprisingly narrow range of observed average heterozygosities, given the great variation in population size between species.
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