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Modeling protein evolution with several amino acid replacement matrices depending on site rates
Most protein substitution models use a single amino acid replacement matrix summarizing the biochemical properties of amino acids. However, site evolution is highly heterogeneous and depends on many factors that influence the substitution patterns. In this paper, we investigate the use of different...
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Published in: | Molecular biology and evolution 2012-10, Vol.29 (10), p.2921-2936 |
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description | Most protein substitution models use a single amino acid replacement matrix summarizing the biochemical properties of amino acids. However, site evolution is highly heterogeneous and depends on many factors that influence the substitution patterns. In this paper, we investigate the use of different substitution matrices for different site evolutionary rates. Indeed, the variability of evolutionary rates corresponds to one of the most apparent heterogeneity factors among sites, and there is no reason to assume that the substitution patterns remain identical regardless of the evolutionary rate. We first introduce LG4M, which is composed of four matrices, each corresponding to one discrete gamma rate category (of four). These matrices differ in their amino acid equilibrium distributions and in their exchangeabilities, contrary to the standard gamma model where only the global rate differs from one category to another. Next, we present LG4X, which also uses four different matrices, but leaves aside the gamma distribution and follows a distribution-free scheme for the site rates. All these matrices are estimated from a very large alignment database, and our two models are tested using a large sample of independent alignments. Detailed analysis of resulting matrices and models shows the complexity of amino acid substitutions and the advantage of flexible models such as LG4M and LG4X. Both significantly outperform single-matrix models, providing gains of dozens to hundreds of log-likelihood units for most data sets. LG4X obtains substantial gains compared with LG4M, thanks to its distribution-free scheme for site rates. Since LG4M and LG4X display such advantages but require the same memory space and have comparable running times to standard models, we believe that LG4M and LG4X are relevant alternatives to single replacement matrices. Our models, data, and software are available from http://www.atgc-montpellier.fr/models/lg4x. |
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However, site evolution is highly heterogeneous and depends on many factors that influence the substitution patterns. In this paper, we investigate the use of different substitution matrices for different site evolutionary rates. Indeed, the variability of evolutionary rates corresponds to one of the most apparent heterogeneity factors among sites, and there is no reason to assume that the substitution patterns remain identical regardless of the evolutionary rate. We first introduce LG4M, which is composed of four matrices, each corresponding to one discrete gamma rate category (of four). These matrices differ in their amino acid equilibrium distributions and in their exchangeabilities, contrary to the standard gamma model where only the global rate differs from one category to another. Next, we present LG4X, which also uses four different matrices, but leaves aside the gamma distribution and follows a distribution-free scheme for the site rates. All these matrices are estimated from a very large alignment database, and our two models are tested using a large sample of independent alignments. Detailed analysis of resulting matrices and models shows the complexity of amino acid substitutions and the advantage of flexible models such as LG4M and LG4X. Both significantly outperform single-matrix models, providing gains of dozens to hundreds of log-likelihood units for most data sets. LG4X obtains substantial gains compared with LG4M, thanks to its distribution-free scheme for site rates. Since LG4M and LG4X display such advantages but require the same memory space and have comparable running times to standard models, we believe that LG4M and LG4X are relevant alternatives to single replacement matrices. Our models, data, and software are available from http://www.atgc-montpellier.fr/models/lg4x.</description><identifier>ISSN: 0737-4038</identifier><identifier>EISSN: 1537-1719</identifier><identifier>DOI: 10.1093/molbev/mss112</identifier><identifier>PMID: 22491036</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Algorithms ; Amino Acid Substitution - genetics ; Amino acids ; Biodiversity ; Bioinformatics ; Computer Science ; Databases, Protein ; Evolution & development ; Evolution, Molecular ; Heterogeneity ; Life Sciences ; Likelihood Functions ; Models, Genetic ; Molecular biology ; Mutation Rate ; Populations and Evolution ; Proteins ; Proteins - genetics ; Quantitative Methods ; Time Factors</subject><ispartof>Molecular biology and evolution, 2012-10, Vol.29 (10), p.2921-2936</ispartof><rights>Copyright Oxford Publishing Limited(England) Oct 2012</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-58493f66f9eb19a1ca430497dca3024f70f2c59c570307fe07353940f1d411553</citedby><cites>FETCH-LOGICAL-c396t-58493f66f9eb19a1ca430497dca3024f70f2c59c570307fe07353940f1d411553</cites><orcidid>0000-0002-3715-210X ; 0000-0002-9412-9723</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22491036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal-lirmm.ccsd.cnrs.fr/lirmm-00715443$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Le, Si Quang</creatorcontrib><creatorcontrib>Dang, Cuong Cao</creatorcontrib><creatorcontrib>Gascuel, Olivier</creatorcontrib><title>Modeling protein evolution with several amino acid replacement matrices depending on site rates</title><title>Molecular biology and evolution</title><addtitle>Mol Biol Evol</addtitle><description>Most protein substitution models use a single amino acid replacement matrix summarizing the biochemical properties of amino acids. However, site evolution is highly heterogeneous and depends on many factors that influence the substitution patterns. In this paper, we investigate the use of different substitution matrices for different site evolutionary rates. Indeed, the variability of evolutionary rates corresponds to one of the most apparent heterogeneity factors among sites, and there is no reason to assume that the substitution patterns remain identical regardless of the evolutionary rate. We first introduce LG4M, which is composed of four matrices, each corresponding to one discrete gamma rate category (of four). These matrices differ in their amino acid equilibrium distributions and in their exchangeabilities, contrary to the standard gamma model where only the global rate differs from one category to another. Next, we present LG4X, which also uses four different matrices, but leaves aside the gamma distribution and follows a distribution-free scheme for the site rates. All these matrices are estimated from a very large alignment database, and our two models are tested using a large sample of independent alignments. Detailed analysis of resulting matrices and models shows the complexity of amino acid substitutions and the advantage of flexible models such as LG4M and LG4X. Both significantly outperform single-matrix models, providing gains of dozens to hundreds of log-likelihood units for most data sets. LG4X obtains substantial gains compared with LG4M, thanks to its distribution-free scheme for site rates. Since LG4M and LG4X display such advantages but require the same memory space and have comparable running times to standard models, we believe that LG4M and LG4X are relevant alternatives to single replacement matrices. Our models, data, and software are available from http://www.atgc-montpellier.fr/models/lg4x.</description><subject>Algorithms</subject><subject>Amino Acid Substitution - genetics</subject><subject>Amino acids</subject><subject>Biodiversity</subject><subject>Bioinformatics</subject><subject>Computer Science</subject><subject>Databases, Protein</subject><subject>Evolution & development</subject><subject>Evolution, Molecular</subject><subject>Heterogeneity</subject><subject>Life Sciences</subject><subject>Likelihood Functions</subject><subject>Models, Genetic</subject><subject>Molecular biology</subject><subject>Mutation Rate</subject><subject>Populations and Evolution</subject><subject>Proteins</subject><subject>Proteins - genetics</subject><subject>Quantitative Methods</subject><subject>Time Factors</subject><issn>0737-4038</issn><issn>1537-1719</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpdkT1vFDEQhi0EIpdASYss0SBFS2bW3g-XUUQSpENpQm35vLPEkb0-bO9F_Hv22JCCylM8845fPYx9QPiCoMRFiH5Hh4uQM2L9im2wEV2FHarXbAPdMksQ_Qk7zfkRAKVs27fspK6lQhDthunvcSDvpp98n2IhN3E6RD8XFyf-5MoDz3SgZDw3wU2RG-sGnmjvjaVAU-HBlOQsZT7QnqbhGLRsZleIJ1Mov2NvRuMzvX9-z9iP66_3V7fV9u7m29XltrJCtaVqeqnE2Lajoh0qg9ZIAVJ1gzUCajl2MNa2UbbpQEA30tKsEUrCiINEbBpxxs7X3Afj9T65YNJvHY3Tt5db7V0KQQN02EgpDrjQn1d6Kf1rplx0cNmS92aiOGeN0EPf10qJBf30H_oY5zQtXf5SnQJRH89XK2VTzDnR-PIHBH30pFdPevW08B-fU-ddoOGF_idG_AG5TI8r</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Le, Si Quang</creator><creator>Dang, Cuong Cao</creator><creator>Gascuel, Olivier</creator><general>Oxford University Press</general><general>Oxford University Press (OUP)</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-3715-210X</orcidid><orcidid>https://orcid.org/0000-0002-9412-9723</orcidid></search><sort><creationdate>20121001</creationdate><title>Modeling protein evolution with several amino acid replacement matrices depending on site rates</title><author>Le, Si Quang ; Dang, Cuong Cao ; Gascuel, Olivier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-58493f66f9eb19a1ca430497dca3024f70f2c59c570307fe07353940f1d411553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Algorithms</topic><topic>Amino Acid Substitution - genetics</topic><topic>Amino acids</topic><topic>Biodiversity</topic><topic>Bioinformatics</topic><topic>Computer Science</topic><topic>Databases, Protein</topic><topic>Evolution & development</topic><topic>Evolution, Molecular</topic><topic>Heterogeneity</topic><topic>Life Sciences</topic><topic>Likelihood Functions</topic><topic>Models, Genetic</topic><topic>Molecular biology</topic><topic>Mutation Rate</topic><topic>Populations and Evolution</topic><topic>Proteins</topic><topic>Proteins - genetics</topic><topic>Quantitative Methods</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le, Si Quang</creatorcontrib><creatorcontrib>Dang, Cuong Cao</creatorcontrib><creatorcontrib>Gascuel, Olivier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Molecular biology and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le, Si Quang</au><au>Dang, Cuong Cao</au><au>Gascuel, Olivier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modeling protein evolution with several amino acid replacement matrices depending on site rates</atitle><jtitle>Molecular biology and evolution</jtitle><addtitle>Mol Biol Evol</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>29</volume><issue>10</issue><spage>2921</spage><epage>2936</epage><pages>2921-2936</pages><issn>0737-4038</issn><eissn>1537-1719</eissn><abstract>Most protein substitution models use a single amino acid replacement matrix summarizing the biochemical properties of amino acids. However, site evolution is highly heterogeneous and depends on many factors that influence the substitution patterns. In this paper, we investigate the use of different substitution matrices for different site evolutionary rates. Indeed, the variability of evolutionary rates corresponds to one of the most apparent heterogeneity factors among sites, and there is no reason to assume that the substitution patterns remain identical regardless of the evolutionary rate. We first introduce LG4M, which is composed of four matrices, each corresponding to one discrete gamma rate category (of four). These matrices differ in their amino acid equilibrium distributions and in their exchangeabilities, contrary to the standard gamma model where only the global rate differs from one category to another. Next, we present LG4X, which also uses four different matrices, but leaves aside the gamma distribution and follows a distribution-free scheme for the site rates. All these matrices are estimated from a very large alignment database, and our two models are tested using a large sample of independent alignments. Detailed analysis of resulting matrices and models shows the complexity of amino acid substitutions and the advantage of flexible models such as LG4M and LG4X. Both significantly outperform single-matrix models, providing gains of dozens to hundreds of log-likelihood units for most data sets. LG4X obtains substantial gains compared with LG4M, thanks to its distribution-free scheme for site rates. Since LG4M and LG4X display such advantages but require the same memory space and have comparable running times to standard models, we believe that LG4M and LG4X are relevant alternatives to single replacement matrices. Our models, data, and software are available from http://www.atgc-montpellier.fr/models/lg4x.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>22491036</pmid><doi>10.1093/molbev/mss112</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-3715-210X</orcidid><orcidid>https://orcid.org/0000-0002-9412-9723</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Amino Acid Substitution - genetics Amino acids Biodiversity Bioinformatics Computer Science Databases, Protein Evolution & development Evolution, Molecular Heterogeneity Life Sciences Likelihood Functions Models, Genetic Molecular biology Mutation Rate Populations and Evolution Proteins Proteins - genetics Quantitative Methods Time Factors |
title | Modeling protein evolution with several amino acid replacement matrices depending on site rates |
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