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1: Proc Natl Acad Sci U S A. 2007 Aug 14;104(33):13390-5. Epub 2007 Aug 6.
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Accumulation of slightly deleterious mutations in mitochondrial protein-coding genes of large versus small mammals.

Popadin K, Polishchuk LV, Mamirova L, Knorre D, Gunbin K.

Departments of Genetics, Biological Faculty of M.V. Lomonosov Moscow State University, Vorobyevy Gory 1-12, Moscow 119992, Russia. konstantinpopadin@gmail.com

After the effective size of a population, N(e), declines, some slightly deleterious amino acid replacements which were initially suppressed by purifying selection become effectively neutral and can reach fixation. Here we investigate this phenomenon for a set of all 13 mitochondrial protein-coding genes from 110 mammalian species. By using body mass as a proxy for N(e), we show that large mammals (i.e., those with low N(e)) as compared with small ones (in our sample these are, on average, 369.5 kg and 275 g, respectively) have a 43% higher rate of accumulation of nonsynonymous nucleotide substitutions relative to synonymous substitutions, and an 8-40% higher rate of accumulation of radical amino acid substitutions relative to conservative substitutions, depending on the type of amino acid classification. These higher rates result in a 6% greater amino acid dissimilarity between modern species and their most recent reconstructed ancestors in large versus small mammals. Because nonsynonymous substitutions are likely to be more harmful than synonymous substitutions, and radical amino acid substitutions are likely to be more harmful than conservative ones, our results suggest that large mammals experience less efficient purifying selection than small mammals. Furthermore, because in the course of mammalian evolution body size tends to increase and, consequently, N(e) tends to decline, evolution of mammals toward large body size may involve accumulation of slightly deleterious mutations in mitochondrial protein-coding genes, which may contribute to decline or extinction of large mammals.

Publication Types:
PMID: 17679693 [PubMed - indexed for MEDLINE]

PMCID: PMC1948928