Direct estimation of the mitochondrial DNA mutation rate in Drosophila melanogaster

被引:223
|
作者
Haag-Liautard, Cathy [1 ]
Coffey, Nicole [2 ]
Houle, David [3 ]
Lynch, Michael [2 ]
Charlesworth, Brian [1 ]
Keightley, Peter D. [1 ]
机构
[1] Univ Edinburgh, Sch Biol Sci, Inst Evolutionary Biol, Edinburgh, Midlothian, Scotland
[2] Indiana Univ, Dept Biol, Bloomington, IN USA
[3] Florida State Univ, Dept Biol Sci, Tallahassee, FL 32306 USA
来源
PLOS BIOLOGY | 2008年 / 6卷 / 08期
基金
英国惠康基金; 美国国家卫生研究院; 加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
D O I
10.1371/journal.pbio.0060204
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial DNA (mtDNA) variants are widely used in evolutionary genetics as markers for population history and to estimate divergence times among taxa. Inferences of species history are generally based on phylogenetic comparisons, which assume that molecular evolution is clock-like. Between-species comparisons have also been used to estimate the mutation rate, using sites that are thought to evolve neutrally. We directly estimated the mtDNA mutation rate by scanning the mitochondrial genome of Drosophila melanogaster lines that had undergone approximately 200 generations of spontaneous mutation accumulation (MA). We detected a total of 28 point mutations and eight insertion-deletion (indel) mutations, yielding an estimate for the single-nucleotide mutation rate of 6.2 x 10(-8) per site per fly generation. Most mutations were heteroplasmic within a line, and their frequency distribution suggests that the effective number of mitochondrial genomes transmitted per female per generation is about 30. We observed repeated occurrences of some indel mutations, suggesting that indel mutational hotspots are common. Among the point mutations, there is a large excess of G -> A mutations on the major strand (the sense strand for the majority of mitochondrial genes). These mutations tend to occur at nonsynonymous sites of protein-coding genes, and they are expected to be deleterious, so do not become fixed between species. The overall mtDNA mutation rate per base pair per fly generation in Drosophila is estimated to be about 10x higher than the nuclear mutation rate, but the mitochondrial major strand G -> A mutation rate is about 70x higher than the nuclear rate. Silent sites are substantially more strongly biased towards A and T than nonsynonymous sites, consistent with the extreme mutation bias towards A+T. Strand-asymmetric mutation bias, coupled with selection to maintain specific nonsynonymous bases, therefore provides an explanation for the extreme base composition of the mitochondrial genome of Drosophila.
引用
收藏
页码:1706 / 1714
页数:9
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