Relative rates of evolution of male-beneficial nuclear compensatory mutations and male-harming Mother's Curse mitochondrial alleles

被引:1
作者
Dapper, Amy L. [1 ,4 ]
Diegel, Amanda E. [2 ]
Wade, Michael J. [3 ]
机构
[1] Mississippi State Univ, Dept Biol Sci, Mississippi State, MS USA
[2] Mississippi State Univ, Dept Math & Stat, Mississippi State, MS USA
[3] Indiana Univ, Dept Biol, Bloomington, IN USA
[4] Mississippi State Univ, Dept Biol Sci, 325 E Lee Blvd, Mississippi State, MS 39762 USA
基金
美国国家科学基金会; 美国农业部;
关键词
models/simulations; molecular evolution; population structure; population genetics; mutations; MULLERS RATCHET; MATERNAL INHERITANCE; POPULATION-GENETICS; CLONAL INTERFERENCE; MULTIPLE PATERNITY; SELECTION; LOAD; FITNESS; GENOME; COMPETITION;
D O I
10.1093/evolut/qpad087
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Mother's Curse alleles represent a significant source of potential male fitness defects. The maternal inheritance of mutations with the pattern of sex-specific fitness effects, s(?) > 0 > s(?), allows Mother's Curse alleles to spread through a population even though they reduce male fitness. Although the mitochondrial genomes of animals contain only a handful of protein-coding genes, mutations in many of these genes have been shown to have a direct effect on male fertility. The evolutionary process of nuclear compensation is hypothesized to counteract the male-limited mitochondrial defects that spread via Mother's Curse. Here we use population genetic models to investigate the evolution of compensatory autosomal nuclear mutations that act to restore the loss of fitness caused by mitochondrial mutation pressures. We derive the rate of male fitness deterioration by Mother's Curse and the rate of restoration by nuclear compensatory evolution. We find that the rate of nuclear gene compensation is many times slower than that of its deterioration by cytoplasmic mutation pressure, resulting in a significant lag in the recovery of male fitness. Thus, the numbers of nuclear genes capable of restoring male mitochondrial fitness defects must be large in order to sustain male fitness in the face of mutation pressures.
引用
收藏
页码:1945 / 1955
页数:11
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