Strong purifying selection in transmission of mammalian mitochondrial DNA

被引:391
作者
Stewart, James Bruce [1 ]
Freyer, Christoph [1 ]
Elson, Joanna L. [2 ]
Wredenberg, Anna [1 ]
Cansu, Zekiye [1 ]
Trifunovic, Aleksandra [1 ]
Larsson, Nils-Goeran [1 ]
机构
[1] Karolinska Inst, Dept Lab Med, Stockholm, Sweden
[2] Newcastle Univ, Sch Med, Mitochondrial Res Grp, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国医学研究理事会;
关键词
D O I
10.1371/journal.pbio.0060010
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
There is an intense debate concerning whether selection or demographics has been most important in shaping the sequence variation observed in modern human mitochondrial DNA (mtDNA). Purifying selection is thought to be important in shaping mtDNA sequence evolution, but the strength of this selection has been debated, mainly due to the threshold effect of pathogenic mtDNA mutations and an observed excess of new mtDNA mutations in human population data. We experimentally addressed this issue by studying the maternal transmission of random mtDNA mutations in mtDNA mutator mice expressing a proofreading-deficient mitochondrial DNA polymerase. We report a rapid and strong elimination of nonsynonymous changes in protein-coding genes; the hallmark of purifying selection. There are striking similarities between the mutational patterns in our experimental mouse system and human mtDNA polymorphisms. These data show strong purifying selection against mutations within mtDNA protein-coding genes. To our knowledge, our study presents the first direct experimental observations of the fate of random mtDNA mutations in the mammalian germ line and demonstrates the importance of purifying selection in shaping mitochondrial sequence diversity.
引用
收藏
页码:63 / 71
页数:9
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