Abstract
AbstractHuman evolutionary genetics gives a chronological framework to interpret the human history. It is based on the molecular clock hypothesis that suppose a straightforward relationship between the mutation rate and the substitution rate with independence of other factors as demography dynamics. Analyzing ancient and modern human complete mitochondrial genomes we show here that, along the time, the substitution rate can be significantly slower or faster than the average germline mutation rate confirming a time dependence effect mainly attributable to changes in the effective population size of the human populations, with an exponential growth in recent times. We also detect that transient polymorphisms play a slowdown role in the evolutionary rate deduced from haplogroup intraspecific trees. Finally, we propose the use of the most divergent lineages within haplogroups as a practical approach to correct these molecular clock mismatches.
Publisher
Springer Science and Business Media LLC
Reference54 articles.
1. Zuckerkandl, E. & Pauling, L. Evolving Genes and Proteins 97–166 (Elsevier, Amsterdam, 1965).
2. Arenas, M. Trends in substitution models of molecular evolution. Front. Genet. 6, 319 (2015).
3. Ho, S. Y. W., Phillips, M. J., Cooper, A. & Drummond, A. J. Time dependency of molecular rate estimates and systematic overestimation of recent divergence times. Choos. Appropr. Subst. Models Phylogenet. Anal. Protein-Coding Seq. 22, 1561–1568 (2005).
4. Henn, B. M., Gignoux, C. R., Feldman, M. W. & Mountain, J. L. Characterizing the time dependency of human mitochondrial DNA mutation rate estimates. Mol. Biol. Evol. 26, 217–230 (2009).
5. Leonardi, M. et al. Evolutionary patterns and processes: Lessons from ancient DNA. Syst. Biol. 66, e1–e29 (2017).
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