Epistasis as the primary factor in molecular evolution
A comparison of more than 1,000 orthologues of diverse proteins shows that the rate of amino-acid substitution in recent evolution is an order of magnitude lower than that expected in the absence of epistasis, indicating that epistasis is pervasive throughout protein evolution. Epistasis in protein...
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description | A comparison of more than 1,000 orthologues of diverse proteins shows that the rate of amino-acid substitution in recent evolution is an order of magnitude lower than that expected in the absence of epistasis, indicating that epistasis is pervasive throughout protein evolution.
Epistasis in protein evolution
In this paper, Fyodor Kondrashov and colleagues provide a quantitative estimate of the fraction of amino-acid substitutions in evolution that have been influenced by epistasis — instances in which substitutions that are accepted in one genetic background genotype are deleterious in another. A comparison of more than one thousand orthologues of selected organelle and nuclear genes reveals a rate of amino-acid substitution in recent evolution that is 20 times slower than the rate of neutral evolution — an order of magnitude slower than that expected in the absence of epistasis. These results suggest that most amino-acid substitutions have different fitness effects in different species, and that epistasis provides the primary conceptual framework to describe the mode and tempo of long-term protein evolution.
The main forces directing long-term molecular evolution remain obscure. A sizable fraction of amino-acid substitutions seem to be fixed by positive selection
1
,
2
,
3
,
4
, but it is unclear to what degree long-term protein evolution is constrained by epistasis, that is, instances when substitutions that are accepted in one genotype are deleterious in another. Here we obtain a quantitative estimate of the prevalence of epistasis in long-term protein evolution by relating data on amino-acid usage in 14 organelle proteins and 2 nuclear-encoded proteins to their rates of short-term evolution. We studied multiple alignments of at least 1,000 orthologues for each of these 16 proteins from species from a diverse phylogenetic background and found that an average site contained approximately eight different amino acids. Thus, without epistasis an average site should accept two-fifths of all possible amino acids, and the average rate of amino-acid substitutions should therefore be about three-fifths lower than the rate of neutral evolution. However, we found that the measured rate of amino-acid substitution in recent evolution is 20 times lower than the rate of neutral evolution and an order of magnitude lower than that expected in the absence of epistasis. These data indicate that epistasis is pervasive throughout protein evolution: about 90 per cent of all |
doi_str_mv | 10.1038/nature11510 |
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Epistasis in protein evolution
In this paper, Fyodor Kondrashov and colleagues provide a quantitative estimate of the fraction of amino-acid substitutions in evolution that have been influenced by epistasis — instances in which substitutions that are accepted in one genetic background genotype are deleterious in another. A comparison of more than one thousand orthologues of selected organelle and nuclear genes reveals a rate of amino-acid substitution in recent evolution that is 20 times slower than the rate of neutral evolution — an order of magnitude slower than that expected in the absence of epistasis. These results suggest that most amino-acid substitutions have different fitness effects in different species, and that epistasis provides the primary conceptual framework to describe the mode and tempo of long-term protein evolution.
The main forces directing long-term molecular evolution remain obscure. A sizable fraction of amino-acid substitutions seem to be fixed by positive selection
1
,
2
,
3
,
4
, but it is unclear to what degree long-term protein evolution is constrained by epistasis, that is, instances when substitutions that are accepted in one genotype are deleterious in another. Here we obtain a quantitative estimate of the prevalence of epistasis in long-term protein evolution by relating data on amino-acid usage in 14 organelle proteins and 2 nuclear-encoded proteins to their rates of short-term evolution. We studied multiple alignments of at least 1,000 orthologues for each of these 16 proteins from species from a diverse phylogenetic background and found that an average site contained approximately eight different amino acids. Thus, without epistasis an average site should accept two-fifths of all possible amino acids, and the average rate of amino-acid substitutions should therefore be about three-fifths lower than the rate of neutral evolution. However, we found that the measured rate of amino-acid substitution in recent evolution is 20 times lower than the rate of neutral evolution and an order of magnitude lower than that expected in the absence of epistasis. These data indicate that epistasis is pervasive throughout protein evolution: about 90 per cent of all amino-acid substitutions have a neutral or beneficial impact only in the genetic backgrounds in which they occur, and must therefore be deleterious in a different background of other species. Our findings show that most amino-acid substitutions have different fitness effects in different species and that epistasis provides the primary conceptual framework to describe the tempo and mode of long-term protein evolution.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature11510</identifier><identifier>PMID: 23064225</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/181/735 ; 631/208/191/1471 ; Amino Acid Substitution - genetics ; Amino acids ; Animals ; Biological and medical sciences ; Biological evolution ; Cell Nucleus - genetics ; Computational Biology ; Epistasis, Genetic - genetics ; Evolution, Molecular ; Fundamental and applied biological sciences. Psychology ; Genetic epistasis ; Genetic Fitness ; Genetics of eukaryotes. Biological and molecular evolution ; Genotype ; Humanities and Social Sciences ; letter ; Models, Genetic ; Molecular evolution ; multidisciplinary ; Mutation ; Organelles - genetics ; Phylogeny ; Properties ; Proteins - chemistry ; Proteins - genetics ; Science ; Sequence Alignment ; Species Specificity</subject><ispartof>Nature (London), 2012-10, Vol.490 (7421), p.535-538</ispartof><rights>Springer Nature Limited 2012</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2012 Nature Publishing Group</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c624t-d8dcefd767a38072fd41cec50ac827318301ff3e5507693fd05f111a5af42a0f3</citedby><cites>FETCH-LOGICAL-c624t-d8dcefd767a38072fd41cec50ac827318301ff3e5507693fd05f111a5af42a0f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature11510$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature11510$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26460554$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23064225$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Breen, Michael S.</creatorcontrib><creatorcontrib>Kemena, Carsten</creatorcontrib><creatorcontrib>Vlasov, Peter K.</creatorcontrib><creatorcontrib>Notredame, Cedric</creatorcontrib><creatorcontrib>Kondrashov, Fyodor A.</creatorcontrib><title>Epistasis as the primary factor in molecular evolution</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>A comparison of more than 1,000 orthologues of diverse proteins shows that the rate of amino-acid substitution in recent evolution is an order of magnitude lower than that expected in the absence of epistasis, indicating that epistasis is pervasive throughout protein evolution.
Epistasis in protein evolution
In this paper, Fyodor Kondrashov and colleagues provide a quantitative estimate of the fraction of amino-acid substitutions in evolution that have been influenced by epistasis — instances in which substitutions that are accepted in one genetic background genotype are deleterious in another. A comparison of more than one thousand orthologues of selected organelle and nuclear genes reveals a rate of amino-acid substitution in recent evolution that is 20 times slower than the rate of neutral evolution — an order of magnitude slower than that expected in the absence of epistasis. These results suggest that most amino-acid substitutions have different fitness effects in different species, and that epistasis provides the primary conceptual framework to describe the mode and tempo of long-term protein evolution.
The main forces directing long-term molecular evolution remain obscure. A sizable fraction of amino-acid substitutions seem to be fixed by positive selection
1
,
2
,
3
,
4
, but it is unclear to what degree long-term protein evolution is constrained by epistasis, that is, instances when substitutions that are accepted in one genotype are deleterious in another. Here we obtain a quantitative estimate of the prevalence of epistasis in long-term protein evolution by relating data on amino-acid usage in 14 organelle proteins and 2 nuclear-encoded proteins to their rates of short-term evolution. We studied multiple alignments of at least 1,000 orthologues for each of these 16 proteins from species from a diverse phylogenetic background and found that an average site contained approximately eight different amino acids. Thus, without epistasis an average site should accept two-fifths of all possible amino acids, and the average rate of amino-acid substitutions should therefore be about three-fifths lower than the rate of neutral evolution. However, we found that the measured rate of amino-acid substitution in recent evolution is 20 times lower than the rate of neutral evolution and an order of magnitude lower than that expected in the absence of epistasis. These data indicate that epistasis is pervasive throughout protein evolution: about 90 per cent of all amino-acid substitutions have a neutral or beneficial impact only in the genetic backgrounds in which they occur, and must therefore be deleterious in a different background of other species. Our findings show that most amino-acid substitutions have different fitness effects in different species and that epistasis provides the primary conceptual framework to describe the tempo and mode of long-term protein evolution.</description><subject>631/181/735</subject><subject>631/208/191/1471</subject><subject>Amino Acid Substitution - genetics</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological evolution</subject><subject>Cell Nucleus - genetics</subject><subject>Computational Biology</subject><subject>Epistasis, Genetic - genetics</subject><subject>Evolution, Molecular</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic epistasis</subject><subject>Genetic Fitness</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Genotype</subject><subject>Humanities and Social Sciences</subject><subject>letter</subject><subject>Models, Genetic</subject><subject>Molecular evolution</subject><subject>multidisciplinary</subject><subject>Mutation</subject><subject>Organelles - genetics</subject><subject>Phylogeny</subject><subject>Properties</subject><subject>Proteins - chemistry</subject><subject>Proteins - genetics</subject><subject>Science</subject><subject>Sequence Alignment</subject><subject>Species Specificity</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10k2LFDEQBuAgijuunrxLo3gQ7bWSzpfHYVh1YVHQFY-hTCdjlu70mKRF_72RGXUHWnIIJE-qCG8R8pDCGYVOv4xY5uQoFRRukRXlSrZcanWbrACYbkF38oTcy_kaAARV_C45YR1IzphYEXm-C7lgDrnB3JSvrtmlMGL62Xi0ZUpNiM04Dc7OA6bGfZ-GuYQp3id3PA7ZPTjsp-TT6_Orzdv28v2bi836srWS8dL2urfO90oq7DQo5ntOrbMC0GqmOqo7oN53TghQ8lXnexCeUooCPWcIvjslT_Z1tzg4E6KfSkI7hmzNuv5BCSU1q6pdUFsXXcJhis6HenzkHy94uwvfzE10toDq6t0Y7GLVZ0cPqinuR9ninLO5-Pjh2D7_v11ffd68W9Q2TTkn580hJEPB_J4Bc2MGqn6017v5y-j6v_ZP6BU8PQDMFgefMNqQ_znJJQjBq3uxd7lexa1L5nqaU6x5L_b9BZJixDQ</recordid><startdate>20121025</startdate><enddate>20121025</enddate><creator>Breen, Michael S.</creator><creator>Kemena, Carsten</creator><creator>Vlasov, Peter K.</creator><creator>Notredame, Cedric</creator><creator>Kondrashov, Fyodor A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ATWCN</scope></search><sort><creationdate>20121025</creationdate><title>Epistasis as the primary factor in molecular evolution</title><author>Breen, Michael S. ; Kemena, Carsten ; Vlasov, Peter K. ; Notredame, Cedric ; Kondrashov, Fyodor A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c624t-d8dcefd767a38072fd41cec50ac827318301ff3e5507693fd05f111a5af42a0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>631/181/735</topic><topic>631/208/191/1471</topic><topic>Amino Acid Substitution - genetics</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological evolution</topic><topic>Cell Nucleus - genetics</topic><topic>Computational Biology</topic><topic>Epistasis, Genetic - genetics</topic><topic>Evolution, Molecular</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic epistasis</topic><topic>Genetic Fitness</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Genotype</topic><topic>Humanities and Social Sciences</topic><topic>letter</topic><topic>Models, Genetic</topic><topic>Molecular evolution</topic><topic>multidisciplinary</topic><topic>Mutation</topic><topic>Organelles - genetics</topic><topic>Phylogeny</topic><topic>Properties</topic><topic>Proteins - chemistry</topic><topic>Proteins - genetics</topic><topic>Science</topic><topic>Sequence Alignment</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Breen, Michael S.</creatorcontrib><creatorcontrib>Kemena, Carsten</creatorcontrib><creatorcontrib>Vlasov, Peter K.</creatorcontrib><creatorcontrib>Notredame, Cedric</creatorcontrib><creatorcontrib>Kondrashov, Fyodor A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Middle School</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Breen, Michael S.</au><au>Kemena, Carsten</au><au>Vlasov, Peter K.</au><au>Notredame, Cedric</au><au>Kondrashov, Fyodor A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epistasis as the primary factor in molecular evolution</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2012-10-25</date><risdate>2012</risdate><volume>490</volume><issue>7421</issue><spage>535</spage><epage>538</epage><pages>535-538</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>A comparison of more than 1,000 orthologues of diverse proteins shows that the rate of amino-acid substitution in recent evolution is an order of magnitude lower than that expected in the absence of epistasis, indicating that epistasis is pervasive throughout protein evolution.
Epistasis in protein evolution
In this paper, Fyodor Kondrashov and colleagues provide a quantitative estimate of the fraction of amino-acid substitutions in evolution that have been influenced by epistasis — instances in which substitutions that are accepted in one genetic background genotype are deleterious in another. A comparison of more than one thousand orthologues of selected organelle and nuclear genes reveals a rate of amino-acid substitution in recent evolution that is 20 times slower than the rate of neutral evolution — an order of magnitude slower than that expected in the absence of epistasis. These results suggest that most amino-acid substitutions have different fitness effects in different species, and that epistasis provides the primary conceptual framework to describe the mode and tempo of long-term protein evolution.
The main forces directing long-term molecular evolution remain obscure. A sizable fraction of amino-acid substitutions seem to be fixed by positive selection
1
,
2
,
3
,
4
, but it is unclear to what degree long-term protein evolution is constrained by epistasis, that is, instances when substitutions that are accepted in one genotype are deleterious in another. Here we obtain a quantitative estimate of the prevalence of epistasis in long-term protein evolution by relating data on amino-acid usage in 14 organelle proteins and 2 nuclear-encoded proteins to their rates of short-term evolution. We studied multiple alignments of at least 1,000 orthologues for each of these 16 proteins from species from a diverse phylogenetic background and found that an average site contained approximately eight different amino acids. Thus, without epistasis an average site should accept two-fifths of all possible amino acids, and the average rate of amino-acid substitutions should therefore be about three-fifths lower than the rate of neutral evolution. However, we found that the measured rate of amino-acid substitution in recent evolution is 20 times lower than the rate of neutral evolution and an order of magnitude lower than that expected in the absence of epistasis. These data indicate that epistasis is pervasive throughout protein evolution: about 90 per cent of all amino-acid substitutions have a neutral or beneficial impact only in the genetic backgrounds in which they occur, and must therefore be deleterious in a different background of other species. Our findings show that most amino-acid substitutions have different fitness effects in different species and that epistasis provides the primary conceptual framework to describe the tempo and mode of long-term protein evolution.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23064225</pmid><doi>10.1038/nature11510</doi><tpages>4</tpages></addata></record> |
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subjects | 631/181/735 631/208/191/1471 Amino Acid Substitution - genetics Amino acids Animals Biological and medical sciences Biological evolution Cell Nucleus - genetics Computational Biology Epistasis, Genetic - genetics Evolution, Molecular Fundamental and applied biological sciences. Psychology Genetic epistasis Genetic Fitness Genetics of eukaryotes. Biological and molecular evolution Genotype Humanities and Social Sciences letter Models, Genetic Molecular evolution multidisciplinary Mutation Organelles - genetics Phylogeny Properties Proteins - chemistry Proteins - genetics Science Sequence Alignment Species Specificity |
title | Epistasis as the primary factor in molecular evolution |
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