Dobzhansky-Muller incompatibilities in protein evolution

被引:226
作者
Kondrashov, AS
Sunyaev, S
Kondrashov, FA [1 ]
机构
[1] NIH, Natl Ctr Biotechnol Informat, Bethesda, MD 20894 USA
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
D O I
10.1073/pnas.232565499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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, approximate to10% 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 approximate to10 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.
引用
收藏
页码:14878 / 14883
页数:6
相关论文
共 54 条
[1]   Detection of conserved physico-chemical characteristics of proteins by analyzing clusters of positions with co-ordinated substitutions [J].
Afonnikov, DA ;
Oshchepkov, DY ;
Kolchanov, NA .
BIOINFORMATICS, 2001, 17 (11) :1035-1046
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]  
[Anonymous], 6TH P INT C GEN
[5]   Analysis of suppressor mutation reveals long distance interactions in the bc1 complex of Saccharomyces cerevisiae [J].
Brasseur, G ;
Di Rago, JP ;
Slonimski, PP ;
Lemesle-Meunier, D .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2001, 1506 (02) :89-102
[6]  
Chen RD, 1996, PROTEIN SCI, V5, P287
[7]   RNA secondary structure and compensatory evolution [J].
Chen, Y ;
Carlini, DB ;
Baines, JF ;
Parsch, J ;
Braverman, JM ;
Tanda, S ;
Stephan, W .
GENES & GENETIC SYSTEMS, 1999, 74 (06) :271-286
[8]   The evolutionary genetics of speciation [J].
Coyne, JA ;
Orr, HA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1998, 353 (1366) :287-305
[9]   Intragenic suppressors of Hsp70 mutants: Interplay between the ATPase- and peptide-binding domains [J].
Davis, JE ;
Voisine, C ;
Craig, EA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9269-9276
[10]   Progress in predicting inter-residue contacts of proteins with neural networks and correlated mutations [J].
Fariselli, P ;
Olmea, O ;
Valencia, A ;
Casadio, R .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2001, :157-162