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Confirmatory Results

Parallel evolution of metazoan mitochondrial proteins

Galya V. Klink, Georgii A. Bazykin
doi: https://doi.org/10.1101/047274
Galya V. Klink
1Institute for Information Transmission Problems (Kharkevich Institute) of the Russian Academy of Sciences, Moscow 127051, Russia
3Faculty of Bioengineering and Bioinformatics and Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119234, Russia
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Georgii A. Bazykin
1Institute for Information Transmission Problems (Kharkevich Institute) of the Russian Academy of Sciences, Moscow 127051, Russia
2Pirogov Russian National Research Medical University, Moscow 117997, Russia
3Faculty of Bioengineering and Bioinformatics and Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119234, Russia
4Skolkovo Institute of Science and Technology, Skolkovo, 143025, Russia
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  • For correspondence: gbazykin@iitp.ru
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Abstract

Amino acid propensities at amino acid sites change with time due to epistatic interactions or changing environment, affecting the probabilities of fixation of different amino acids. Such changes should lead to an increased rate of homoplasies (reversals, parallelisms, and convergences) at closely related species. Here, we reconstruct the phylogeny of twelve mitochondrial proteins from several thousand metazoan species, and measure the phylogenetic distances between branches at which either different alleles originated due to divergent substitutions, or the same allele originated repeatedly due to homoplasies. The mean phylogenetic distance between parallel substitutions is ~20% lower than the mean phylogenetic distance between divergent substitutions, indicating that a variant fixed in a species is more likely to be deleterious in more phylogenetically remote species, compared to a more closely related species. These findings are robust to artefacts of phylogenetic reconstruction or of pooling of sites from different conservation classes or functional groups, and show that single-position fitness landscapes change at rates similar to rates of amino acid changes.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted April 08, 2016.
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Parallel evolution of metazoan mitochondrial proteins
Galya V. Klink, Georgii A. Bazykin
bioRxiv 047274; doi: https://doi.org/10.1101/047274
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Parallel evolution of metazoan mitochondrial proteins
Galya V. Klink, Georgii A. Bazykin
bioRxiv 047274; doi: https://doi.org/10.1101/047274

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