Universal pacemaker of genome evolution
A fundamental observation of comparative genomics is that the distribution of evolution rates across the complete sets of orthologous genes in pairs of related genomes remains virtually unchanged throughout the evolution of life, from bacteria to mammals. The most straightforward explanation for the...
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description | A fundamental observation of comparative genomics is that the distribution of evolution rates across the complete sets of orthologous genes in pairs of related genomes remains virtually unchanged throughout the evolution of life, from bacteria to mammals. The most straightforward explanation for the conservation of this distribution appears to be that the relative evolution rates of all genes remain nearly constant, or in other words, that evolutionary rates of different genes are strongly correlated within each evolving genome. This correlation could be explained by a model that we denoted Universal PaceMaker (UPM) of genome evolution. The UPM model posits that the rate of evolution changes synchronously across genome-wide sets of genes in all evolving lineages. Alternatively, however, the correlation between the evolutionary rates of genes could be a simple consequence of molecular clock (MC). We sought to differentiate between the MC and UPM models by fitting thousands of phylogenetic trees for bacterial and archaeal genes to supertrees that reflect the dominant trend of vertical descent in the evolution of archaea and bacteria and that were constrained according to the two models. The goodness of fit for the UPM model was better than the fit for the MC model, with overwhelming statistical significance, although similarly to the MC, the UPM is strongly overdispersed. Thus, the results of this analysis reveal a universal, genome-wide pacemaker of evolution that could have been in operation throughout the history of life. |
doi_str_mv | 10.1371/journal.pcbi.1002785 |
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The most straightforward explanation for the conservation of this distribution appears to be that the relative evolution rates of all genes remain nearly constant, or in other words, that evolutionary rates of different genes are strongly correlated within each evolving genome. This correlation could be explained by a model that we denoted Universal PaceMaker (UPM) of genome evolution. The UPM model posits that the rate of evolution changes synchronously across genome-wide sets of genes in all evolving lineages. Alternatively, however, the correlation between the evolutionary rates of genes could be a simple consequence of molecular clock (MC). We sought to differentiate between the MC and UPM models by fitting thousands of phylogenetic trees for bacterial and archaeal genes to supertrees that reflect the dominant trend of vertical descent in the evolution of archaea and bacteria and that were constrained according to the two models. The goodness of fit for the UPM model was better than the fit for the MC model, with overwhelming statistical significance, although similarly to the MC, the UPM is strongly overdispersed. Thus, the results of this analysis reveal a universal, genome-wide pacemaker of evolution that could have been in operation throughout the history of life.</description><identifier>ISSN: 1553-7358</identifier><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1002785</identifier><identifier>PMID: 23209393</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Bacteria ; Biology ; Comparative analysis ; Computational Biology ; Evolution ; Evolution, Molecular ; Evolutionary genetics ; Genome, Archaeal - genetics ; Genome, Bacterial - genetics ; Genomes ; Genomics ; Least-Squares Analysis ; Mitochondrial DNA ; Models, Genetic ; Phylogenetics ; Phylogeny ; Studies</subject><ispartof>PLoS computational biology, 2012-11, Vol.8 (11), p.e1002785-e1002785</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Citation: Snir S, Wolf YI, Koonin EV (2012) Universal Pacemaker of Genome Evolution. PLoS Comput Biol 8(11): e1002785. doi:10.1371/journal.pcbi.1002785</rights><rights>2012</rights><rights>2012 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Citation: Snir S, Wolf YI, Koonin EV (2012) Universal Pacemaker of Genome Evolution. 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The goodness of fit for the UPM model was better than the fit for the MC model, with overwhelming statistical significance, although similarly to the MC, the UPM is strongly overdispersed. Thus, the results of this analysis reveal a universal, genome-wide pacemaker of evolution that could have been in operation throughout the history of life.</description><subject>Bacteria</subject><subject>Biology</subject><subject>Comparative analysis</subject><subject>Computational Biology</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Evolutionary genetics</subject><subject>Genome, Archaeal - genetics</subject><subject>Genome, Bacterial - genetics</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Least-Squares Analysis</subject><subject>Mitochondrial DNA</subject><subject>Models, Genetic</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Studies</subject><issn>1553-7358</issn><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqVkk1v1DAQhi0Eou3CP0CwEgfoYRfbY8fJBamqoF2pAgnK2XL8Ebwk8dZOVvTf4-2mVRdxwXOwNX7mHc94EHpF8JKAIB_WYYy9apcbXfslwZiKkj9Bx4RzWAjg5dNH5yN0ktIa43ysiufoiALFFVRwjN796P3WxqTa-UZp26lfNs6Dmze2D52d221ox8GH_gV65lSb7Mtpn6Hrz5-uzy8XV18vVudnVwtdAAwLZlzNhdEFM7WgzKhCc6YrRopSUcoo8Kp2psLCOF0SWxY1UBCM4EppBgZm6M1edtOGJKcSkySQreRMiEys9oQJai030Xcq3sqgvLxzhNhIFQevWystKRxgVeZUlHGlS0ccw0JzXVFMa5q1Pk7ZxrqzRtt-iKo9ED286f1P2YStBJ4bXrEs8H4SiOFmtGmQnU_atq3qbRjzu2lewBnhGX37F_rv6pZ7qlG5AN-7kPPqbMZ2XofeOp_9Z0AoJmz3gzN0ehCQmcH-Hho1piRX37_9B_vlkGV7VseQUrTuoSsEy9383T9f7uZPTvOXw14_7uhD0P3AwR_AItTq</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Snir, Sagi</creator><creator>Wolf, Yuri I</creator><creator>Koonin, Eugene V</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AL</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0N</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20121101</creationdate><title>Universal pacemaker of genome evolution</title><author>Snir, Sagi ; Wolf, Yuri I ; Koonin, Eugene V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c633t-4dfb57dc64db724da6c54c94168a2242359bfd907dfc81e86b32374109ac43d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Bacteria</topic><topic>Biology</topic><topic>Comparative analysis</topic><topic>Computational Biology</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Evolutionary genetics</topic><topic>Genome, Archaeal - genetics</topic><topic>Genome, Bacterial - genetics</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Least-Squares Analysis</topic><topic>Mitochondrial DNA</topic><topic>Models, Genetic</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Snir, Sagi</creatorcontrib><creatorcontrib>Wolf, Yuri I</creatorcontrib><creatorcontrib>Koonin, Eugene V</creatorcontrib><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: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Computing Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Computing Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS computational biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Snir, Sagi</au><au>Wolf, Yuri I</au><au>Koonin, Eugene V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Universal pacemaker of genome evolution</atitle><jtitle>PLoS computational biology</jtitle><addtitle>PLoS Comput Biol</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>8</volume><issue>11</issue><spage>e1002785</spage><epage>e1002785</epage><pages>e1002785-e1002785</pages><issn>1553-7358</issn><issn>1553-734X</issn><eissn>1553-7358</eissn><abstract>A fundamental observation of comparative genomics is that the distribution of evolution rates across the complete sets of orthologous genes in pairs of related genomes remains virtually unchanged throughout the evolution of life, from bacteria to mammals. The most straightforward explanation for the conservation of this distribution appears to be that the relative evolution rates of all genes remain nearly constant, or in other words, that evolutionary rates of different genes are strongly correlated within each evolving genome. This correlation could be explained by a model that we denoted Universal PaceMaker (UPM) of genome evolution. The UPM model posits that the rate of evolution changes synchronously across genome-wide sets of genes in all evolving lineages. Alternatively, however, the correlation between the evolutionary rates of genes could be a simple consequence of molecular clock (MC). We sought to differentiate between the MC and UPM models by fitting thousands of phylogenetic trees for bacterial and archaeal genes to supertrees that reflect the dominant trend of vertical descent in the evolution of archaea and bacteria and that were constrained according to the two models. The goodness of fit for the UPM model was better than the fit for the MC model, with overwhelming statistical significance, although similarly to the MC, the UPM is strongly overdispersed. Thus, the results of this analysis reveal a universal, genome-wide pacemaker of evolution that could have been in operation throughout the history of life.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23209393</pmid><doi>10.1371/journal.pcbi.1002785</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Biology Comparative analysis Computational Biology Evolution Evolution, Molecular Evolutionary genetics Genome, Archaeal - genetics Genome, Bacterial - genetics Genomes Genomics Least-Squares Analysis Mitochondrial DNA Models, Genetic Phylogenetics Phylogeny Studies |
title | Universal pacemaker of genome evolution |
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