Rapid Evolution of Expression and Regulatory Divergences after Yeast Gene Duplication
Although gene duplication is widely believed to be the major source of genetic novelty, how the expression or regulatory network of duplicate genes evolves remains poorly understood. In this article, we propose an additive expression distance between duplicate genes, so that the evolutionary rate of...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2005-01, Vol.102 (3), p.707-712 |
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description | Although gene duplication is widely believed to be the major source of genetic novelty, how the expression or regulatory network of duplicate genes evolves remains poorly understood. In this article, we propose an additive expression distance between duplicate genes, so that the evolutionary rate of expression divergence after gene duplication can be estimated through phylogenomic analysis. We have analyzed yeast genome sequences, microarrays, and transcriptional regulatory networks, showing a >10-fold increase in the initial rate for both expression and regulatory network evolution after gene duplication but only an ≈20% rate increase in the early stage for protein sequences. Based on the estimated age distribution of yeast duplicate genes, we roughly estimate that the initial rate of expression divergence shortly after gene duplication is 2.9× 10-9per year, whereas the baseline rate for very ancient gene duplication is 0.14× 10-9per year. Relative expression rate tests suggest that the expression of duplicate genes tends to evolve asymmetrically, that is, the expression of one copy evolves rapidly, whereas the other one largely maintains the ancestral expression profile. Our study highlights the crucial role of early rapid evolution after gene/genome duplication for continuously increasing the complexity of the yeast regulatory network. |
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In this article, we propose an additive expression distance between duplicate genes, so that the evolutionary rate of expression divergence after gene duplication can be estimated through phylogenomic analysis. We have analyzed yeast genome sequences, microarrays, and transcriptional regulatory networks, showing a >10-fold increase in the initial rate for both expression and regulatory network evolution after gene duplication but only an ≈20% rate increase in the early stage for protein sequences. Based on the estimated age distribution of yeast duplicate genes, we roughly estimate that the initial rate of expression divergence shortly after gene duplication is 2.9× 10-9per year, whereas the baseline rate for very ancient gene duplication is 0.14× 10-9per year. Relative expression rate tests suggest that the expression of duplicate genes tends to evolve asymmetrically, that is, the expression of one copy evolves rapidly, whereas the other one largely maintains the ancestral expression profile. Our study highlights the crucial role of early rapid evolution after gene/genome duplication for continuously increasing the complexity of the yeast regulatory network.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0409186102</identifier><identifier>PMID: 15647348</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Age distribution ; Arrays ; Biological Sciences ; Divergent evolution ; Duplicate genes ; Evolution ; Evolution, Molecular ; Gene Duplication ; Gene expression ; Gene Expression Regulation - genetics ; Genes ; Genetics ; Kinetics ; Models, Genetic ; P values ; Phylogenetics ; Phylogeny ; Statistical variance ; Yeast ; Yeasts ; Yeasts - cytology ; Yeasts - genetics</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2005-01, Vol.102 (3), p.707-712</ispartof><rights>Copyright 1993/2005 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jan 18, 2005</rights><rights>Copyright © 2005, The National Academy of Sciences 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-9edab86213a92e1233f6b1d30ef11602e4bbc07195bc2db5374e3565839fe59a3</citedby><cites>FETCH-LOGICAL-c588t-9edab86213a92e1233f6b1d30ef11602e4bbc07195bc2db5374e3565839fe59a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/102/3.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3374313$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3374313$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,725,778,782,801,883,27907,27908,53774,53776,58000,58233</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15647348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gu, Xun</creatorcontrib><creatorcontrib>Zhang, Zhongqi</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><creatorcontrib>Tan, Jiazhen</creatorcontrib><title>Rapid Evolution of Expression and Regulatory Divergences after Yeast Gene Duplication</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Although gene duplication is widely believed to be the major source of genetic novelty, how the expression or regulatory network of duplicate genes evolves remains poorly understood. In this article, we propose an additive expression distance between duplicate genes, so that the evolutionary rate of expression divergence after gene duplication can be estimated through phylogenomic analysis. We have analyzed yeast genome sequences, microarrays, and transcriptional regulatory networks, showing a >10-fold increase in the initial rate for both expression and regulatory network evolution after gene duplication but only an ≈20% rate increase in the early stage for protein sequences. Based on the estimated age distribution of yeast duplicate genes, we roughly estimate that the initial rate of expression divergence shortly after gene duplication is 2.9× 10-9per year, whereas the baseline rate for very ancient gene duplication is 0.14× 10-9per year. Relative expression rate tests suggest that the expression of duplicate genes tends to evolve asymmetrically, that is, the expression of one copy evolves rapidly, whereas the other one largely maintains the ancestral expression profile. Our study highlights the crucial role of early rapid evolution after gene/genome duplication for continuously increasing the complexity of the yeast regulatory network.</description><subject>Age distribution</subject><subject>Arrays</subject><subject>Biological Sciences</subject><subject>Divergent evolution</subject><subject>Duplicate genes</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Gene Duplication</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - genetics</subject><subject>Genes</subject><subject>Genetics</subject><subject>Kinetics</subject><subject>Models, Genetic</subject><subject>P values</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Statistical variance</subject><subject>Yeast</subject><subject>Yeasts</subject><subject>Yeasts - cytology</subject><subject>Yeasts - genetics</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EokvhzAWQ1QO3tP6M7QMH1C4FqRJS1R56spxksmSVjYPtrNr_vo521S0IiZPHmt97mpmH0HtKTilR_GwcXDwlghiqS0rYC7SguS5KYchLtCCEqUILJo7QmxjXhBAjNXmNjqgsheJCL9DttRu7Bi-3vp9S5wfsW7y8HwPEOP_c0OBrWE29Sz484ItuC2EFQw0RuzZBwHfgYsKXMAC-mMa-q93s8ha9al0f4d3-PUa335Y359-Lq5-XP86_XhW11DoVBhpX6ZJR7gwDyjhvy4o2nEBLaUkYiKqqiaJGVjVrKsmVAC5LqblpQRrHj9GXne84VRtoahhScL0dQ7dx4cF619k_O0P3y6781kohpWJZ_3mvD_73BDHZTRdr6Hs3gJ-iLRVXmkvxX5CqfH8jZ8eTv8C1n8KQj2AZoSxPrlWGznZQHXyMAdqniSmxc652ztUecs2KT88XPfD7IDPwcQ_MyoMds9wqop4t8M--bae-T3CfMvhhB65jjvyJ5Pn2nHL-CL3ev-k</recordid><startdate>20050118</startdate><enddate>20050118</enddate><creator>Gu, Xun</creator><creator>Zhang, Zhongqi</creator><creator>Huang, Wei</creator><creator>Tan, Jiazhen</creator><general>National Academy of Sciences</general><general>National Acad Sciences</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</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>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20050118</creationdate><title>Rapid Evolution of Expression and Regulatory Divergences after Yeast Gene Duplication</title><author>Gu, Xun ; Zhang, Zhongqi ; Huang, Wei ; Tan, Jiazhen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-9edab86213a92e1233f6b1d30ef11602e4bbc07195bc2db5374e3565839fe59a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age distribution</topic><topic>Arrays</topic><topic>Biological Sciences</topic><topic>Divergent evolution</topic><topic>Duplicate genes</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Gene Duplication</topic><topic>Gene expression</topic><topic>Gene Expression Regulation - genetics</topic><topic>Genes</topic><topic>Genetics</topic><topic>Kinetics</topic><topic>Models, Genetic</topic><topic>P values</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Statistical variance</topic><topic>Yeast</topic><topic>Yeasts</topic><topic>Yeasts - cytology</topic><topic>Yeasts - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Xun</creatorcontrib><creatorcontrib>Zhang, Zhongqi</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><creatorcontrib>Tan, Jiazhen</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Xun</au><au>Zhang, Zhongqi</au><au>Huang, Wei</au><au>Tan, Jiazhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Evolution of Expression and Regulatory Divergences after Yeast Gene Duplication</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2005-01-18</date><risdate>2005</risdate><volume>102</volume><issue>3</issue><spage>707</spage><epage>712</epage><pages>707-712</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Although gene duplication is widely believed to be the major source of genetic novelty, how the expression or regulatory network of duplicate genes evolves remains poorly understood. In this article, we propose an additive expression distance between duplicate genes, so that the evolutionary rate of expression divergence after gene duplication can be estimated through phylogenomic analysis. We have analyzed yeast genome sequences, microarrays, and transcriptional regulatory networks, showing a >10-fold increase in the initial rate for both expression and regulatory network evolution after gene duplication but only an ≈20% rate increase in the early stage for protein sequences. Based on the estimated age distribution of yeast duplicate genes, we roughly estimate that the initial rate of expression divergence shortly after gene duplication is 2.9× 10-9per year, whereas the baseline rate for very ancient gene duplication is 0.14× 10-9per year. 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subjects | Age distribution Arrays Biological Sciences Divergent evolution Duplicate genes Evolution Evolution, Molecular Gene Duplication Gene expression Gene Expression Regulation - genetics Genes Genetics Kinetics Models, Genetic P values Phylogenetics Phylogeny Statistical variance Yeast Yeasts Yeasts - cytology Yeasts - genetics |
title | Rapid Evolution of Expression and Regulatory Divergences after Yeast Gene Duplication |
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