Literature DB >> 12403824

Dobzhansky-Muller incompatibilities in protein evolution.

Alexey S Kondrashov1, Shamil Sunyaev, Fyodor A Kondrashov.   

Abstract

We study fitness landscape in the space of protein sequences by relating sets of human pathogenic missense mutations in 32 proteins to amino acid substitutions that occurred in the course of evolution of these proteins. On average, approximately 10% of deviations of a nonhuman protein from its human ortholog are compensated pathogenic deviations (CPDs), i.e., are caused by an amino acid substitution that, at this site, would be pathogenic to humans. Normal functioning of a CPD-containing protein must be caused by other, compensatory deviations of the nonhuman species from humans. Together, a CPD and the corresponding compensatory deviation form a Dobzhansky-Muller incompatibility that can be visualized as the corner on a fitness ridge. Thus, proteins evolve along fitness ridges which contain only approximately 10 steps between successive corners. The fraction of CPDs among all deviations of a protein from its human ortholog does not increase with the evolutionary distance between the proteins, indicating that substitutions that carry evolving proteins around these corners occur in rapid succession, driven by positive selection. Data on fitness of interspecies hybrids suggest that the compensatory change that makes a CPD fit usually occurs within the same protein. Data on protein structures and on cooccurrence of amino acids at different sites of multiple orthologous proteins often make it possible to provisionally identify the substitution that compensates a particular CPD.

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Year:  2002        PMID: 12403824      PMCID: PMC137512          DOI: 10.1073/pnas.232565499

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  48 in total

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5.  Natural selection and the concept of a protein space.

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Review 10.  The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases.

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  136 in total

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2.  The nearly neutral and selection theories of molecular evolution under the fisher geometrical framework: substitution rate, population size, and complexity.

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Review 3.  Mutational effects and the evolution of new protein functions.

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4.  Sequence space and the ongoing expansion of the protein universe.

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5.  The population genetics of mutations: good, bad and indifferent.

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6.  Lack of evidence for sign epistasis between beneficial mutations in an RNA bacteriophage.

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Journal:  J Mol Evol       Date:  2010-10-12       Impact factor: 2.395

7.  Estimating the genomewide rate of adaptive protein evolution in Drosophila.

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8.  An empirical test of the concomitantly variable codon hypothesis.

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9.  Compensatory epistasis explored by molecular dynamics simulations.

Authors:  Sérgio F Sousa; Luísa Azevedo; Catarina Serrano; Carla S S Teixeira; David N Cooper; João Carneiro; Mónica Lopes-Marques; Peter D Stenson; António Amorim; Maria J Prata
Journal:  Hum Genet       Date:  2021-06-26       Impact factor: 4.132

10.  The evolution of hybrid incompatibilities along a phylogeny.

Authors:  Richard J Wang; Cécile Ané; Bret A Payseur
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