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Old but not (so) degenerated--slow evolution of largely homomorphic sex chromosomes in ratites
Degeneration of the nonrecombining chromosome is a common feature of sex chromosome evolution, readily evident by the presence of a pair of largely heteromorphic chromosomes, like in eutherian mammals and birds. However, in ratites (order Palaeognathae, including, e.g., ostrich), the Z and W chromos...
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Published in: | Molecular biology and evolution 2014-06, Vol.31 (6), p.1444-1453 |
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description | Degeneration of the nonrecombining chromosome is a common feature of sex chromosome evolution, readily evident by the presence of a pair of largely heteromorphic chromosomes, like in eutherian mammals and birds. However, in ratites (order Palaeognathae, including, e.g., ostrich), the Z and W chromosomes are similar in size and largely undifferentiated, despite avian sex chromosome evolution was initiated > 130 Ma. To better understand what may limit sex chromosome evolution, we performed ostrich transcriptome sequencing and studied genes from the nonrecombining region of the W chromosome. Fourteen gametologous gene pairs present on the W chromosome and Z chromosome were identified, with synonymous sequence divergence of 0.027-0.177. The location of these genes on the Z chromosome was consistent with a sequential increase in divergence, starting 110-157 and ending 24-30 Ma. On the basis of the occurrence of Z-linked genes hemizygous in females, we estimate that about one-third of the Z chromosome does not recombine with the W chromosome in female meiosis. Pairwise d(N)/d(S) between gametologs decreased with age, suggesting strong evolutionary constraint in old gametologs. Lineage-specific d(N)/d(S) was consistently higher in W-linked genes, in accordance with the lower efficacy of selection expected in nonrecombining chromosomes. A higher ratio of GC > AT:AT > GC substitutions in W-linked genes supports a role for GC-biased gene conversion in differentially driving base composition on the two sex chromosomes. A male-to-female (M:F) expression ratio of close to one for recombining genes and close to two for Z-linked genes lacking a W copy show that dosage compensation is essentially absent. Some gametologous genes have retained active expression of the W copy in females (giving a M:F ratio of 1 for the gametologous gene pair), whereas for others W expression has become severely reduced resulting in a M:F ratio of close to 2. These observations resemble the patterns of sex chromosome evolution seen in other avian and mammalian lineages, suggesting similar underlying evolutionary processes, although the rate of sex chromosome differentiation has been atypically low. Lack of dosage compensation may be a factor hindering sex chromosome evolution in this lineage. |
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However, in ratites (order Palaeognathae, including, e.g., ostrich), the Z and W chromosomes are similar in size and largely undifferentiated, despite avian sex chromosome evolution was initiated > 130 Ma. To better understand what may limit sex chromosome evolution, we performed ostrich transcriptome sequencing and studied genes from the nonrecombining region of the W chromosome. Fourteen gametologous gene pairs present on the W chromosome and Z chromosome were identified, with synonymous sequence divergence of 0.027-0.177. The location of these genes on the Z chromosome was consistent with a sequential increase in divergence, starting 110-157 and ending 24-30 Ma. On the basis of the occurrence of Z-linked genes hemizygous in females, we estimate that about one-third of the Z chromosome does not recombine with the W chromosome in female meiosis. Pairwise d(N)/d(S) between gametologs decreased with age, suggesting strong evolutionary constraint in old gametologs. Lineage-specific d(N)/d(S) was consistently higher in W-linked genes, in accordance with the lower efficacy of selection expected in nonrecombining chromosomes. A higher ratio of GC > AT:AT > GC substitutions in W-linked genes supports a role for GC-biased gene conversion in differentially driving base composition on the two sex chromosomes. A male-to-female (M:F) expression ratio of close to one for recombining genes and close to two for Z-linked genes lacking a W copy show that dosage compensation is essentially absent. Some gametologous genes have retained active expression of the W copy in females (giving a M:F ratio of 1 for the gametologous gene pair), whereas for others W expression has become severely reduced resulting in a M:F ratio of close to 2. These observations resemble the patterns of sex chromosome evolution seen in other avian and mammalian lineages, suggesting similar underlying evolutionary processes, although the rate of sex chromosome differentiation has been atypically low. Lack of dosage compensation may be a factor hindering sex chromosome evolution in this lineage.</description><identifier>ISSN: 0737-4038</identifier><identifier>ISSN: 1537-1719</identifier><identifier>EISSN: 1537-1719</identifier><identifier>DOI: 10.1093/molbev/msu101</identifier><identifier>PMID: 24618361</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Base Composition ; biased gene conversion ; Birds ; Chromosomes ; Compensation ; Dosage Compensation, Genetic ; Evolution ; Evolution, Molecular ; evolutionary strata ; Female ; gametologs ; Gender ; Gene Conversion ; Genes ; Male ; Mammals ; Molecular Sequence Data ; nonrecombining chromosome ; Recombination, Genetic ; Sequence Analysis, RNA ; Sex Chromosomes ; Struthioniformes - genetics ; Transcriptome ; W chromosome ; Z chromosome</subject><ispartof>Molecular biology and evolution, 2014-06, Vol.31 (6), p.1444-1453</ispartof><rights>The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>Copyright Oxford Publishing Limited(England) Jun 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-964348ce3307933f1e08a26b6e5e7b96f2638594d7f29951cbc75a86bf49755b3</citedby><cites>FETCH-LOGICAL-c430t-964348ce3307933f1e08a26b6e5e7b96f2638594d7f29951cbc75a86bf49755b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24618361$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-228463$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Yazdi, Homa Papoli</creatorcontrib><creatorcontrib>Ellegren, Hans</creatorcontrib><title>Old but not (so) degenerated--slow evolution of largely homomorphic sex chromosomes in ratites</title><title>Molecular biology and evolution</title><addtitle>Mol Biol Evol</addtitle><description>Degeneration of the nonrecombining chromosome is a common feature of sex chromosome evolution, readily evident by the presence of a pair of largely heteromorphic chromosomes, like in eutherian mammals and birds. However, in ratites (order Palaeognathae, including, e.g., ostrich), the Z and W chromosomes are similar in size and largely undifferentiated, despite avian sex chromosome evolution was initiated > 130 Ma. To better understand what may limit sex chromosome evolution, we performed ostrich transcriptome sequencing and studied genes from the nonrecombining region of the W chromosome. Fourteen gametologous gene pairs present on the W chromosome and Z chromosome were identified, with synonymous sequence divergence of 0.027-0.177. The location of these genes on the Z chromosome was consistent with a sequential increase in divergence, starting 110-157 and ending 24-30 Ma. On the basis of the occurrence of Z-linked genes hemizygous in females, we estimate that about one-third of the Z chromosome does not recombine with the W chromosome in female meiosis. Pairwise d(N)/d(S) between gametologs decreased with age, suggesting strong evolutionary constraint in old gametologs. Lineage-specific d(N)/d(S) was consistently higher in W-linked genes, in accordance with the lower efficacy of selection expected in nonrecombining chromosomes. A higher ratio of GC > AT:AT > GC substitutions in W-linked genes supports a role for GC-biased gene conversion in differentially driving base composition on the two sex chromosomes. A male-to-female (M:F) expression ratio of close to one for recombining genes and close to two for Z-linked genes lacking a W copy show that dosage compensation is essentially absent. Some gametologous genes have retained active expression of the W copy in females (giving a M:F ratio of 1 for the gametologous gene pair), whereas for others W expression has become severely reduced resulting in a M:F ratio of close to 2. These observations resemble the patterns of sex chromosome evolution seen in other avian and mammalian lineages, suggesting similar underlying evolutionary processes, although the rate of sex chromosome differentiation has been atypically low. Lack of dosage compensation may be a factor hindering sex chromosome evolution in this lineage.</description><subject>Animals</subject><subject>Base Composition</subject><subject>biased gene conversion</subject><subject>Birds</subject><subject>Chromosomes</subject><subject>Compensation</subject><subject>Dosage Compensation, Genetic</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>evolutionary strata</subject><subject>Female</subject><subject>gametologs</subject><subject>Gender</subject><subject>Gene Conversion</subject><subject>Genes</subject><subject>Male</subject><subject>Mammals</subject><subject>Molecular Sequence Data</subject><subject>nonrecombining chromosome</subject><subject>Recombination, Genetic</subject><subject>Sequence Analysis, RNA</subject><subject>Sex Chromosomes</subject><subject>Struthioniformes - genetics</subject><subject>Transcriptome</subject><subject>W chromosome</subject><subject>Z chromosome</subject><issn>0737-4038</issn><issn>1537-1719</issn><issn>1537-1719</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0U1vFSEUBmBiNPZaXbo1JG5q4ljO8DGwbFq1Jk26aV1Khpkz907DDFcY-vHvpZnahSthASQPbyAvIe-BfQFm-PEUvMPb4yllYPCCbEDypoIGzEuyYU3ZC8b1AXmT0g1jIIRSr8lBLRRormBDfl36nrq80Dks9CiFT7THLc4Y2wX7qko-3FG8DT4vY5hpGKhv4xb9A92Fqcy4340dTXhPu10s5xQmTHScabk_LpjekldD6xO-e1oPyfW3r1en59XF5fcfpycXVSc4WyqjBBe6Q85ZYzgfAJlua-UUSmycUUOtuJZG9M1QGyOhc10jW63cIEwjpeOH5POam-5wn53dx3Fq44MN7WjPxp8nNsStzdnWtRaKF3608n0MvzOmxU5j6tD7dsaQkwUpQQkB2vwHrXUZYHShH_-hNyHHufy7KC6A10I-Blar6mJIKeLw_Fhg9rFSu1Zq10qL__CUmt2E_bP-2yH_A9GRnYE</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Yazdi, Homa Papoli</creator><creator>Ellegren, Hans</creator><general>Oxford University Press</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>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope></search><sort><creationdate>20140601</creationdate><title>Old but not (so) degenerated--slow evolution of largely homomorphic sex chromosomes in ratites</title><author>Yazdi, Homa Papoli ; Ellegren, Hans</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-964348ce3307933f1e08a26b6e5e7b96f2638594d7f29951cbc75a86bf49755b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Base Composition</topic><topic>biased gene conversion</topic><topic>Birds</topic><topic>Chromosomes</topic><topic>Compensation</topic><topic>Dosage Compensation, Genetic</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>evolutionary strata</topic><topic>Female</topic><topic>gametologs</topic><topic>Gender</topic><topic>Gene Conversion</topic><topic>Genes</topic><topic>Male</topic><topic>Mammals</topic><topic>Molecular Sequence Data</topic><topic>nonrecombining chromosome</topic><topic>Recombination, Genetic</topic><topic>Sequence Analysis, RNA</topic><topic>Sex Chromosomes</topic><topic>Struthioniformes - genetics</topic><topic>Transcriptome</topic><topic>W chromosome</topic><topic>Z chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yazdi, Homa Papoli</creatorcontrib><creatorcontrib>Ellegren, Hans</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>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Molecular biology and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yazdi, Homa Papoli</au><au>Ellegren, Hans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Old but not (so) degenerated--slow evolution of largely homomorphic sex chromosomes in ratites</atitle><jtitle>Molecular biology and evolution</jtitle><addtitle>Mol Biol Evol</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>31</volume><issue>6</issue><spage>1444</spage><epage>1453</epage><pages>1444-1453</pages><issn>0737-4038</issn><issn>1537-1719</issn><eissn>1537-1719</eissn><abstract>Degeneration of the nonrecombining chromosome is a common feature of sex chromosome evolution, readily evident by the presence of a pair of largely heteromorphic chromosomes, like in eutherian mammals and birds. However, in ratites (order Palaeognathae, including, e.g., ostrich), the Z and W chromosomes are similar in size and largely undifferentiated, despite avian sex chromosome evolution was initiated > 130 Ma. To better understand what may limit sex chromosome evolution, we performed ostrich transcriptome sequencing and studied genes from the nonrecombining region of the W chromosome. Fourteen gametologous gene pairs present on the W chromosome and Z chromosome were identified, with synonymous sequence divergence of 0.027-0.177. The location of these genes on the Z chromosome was consistent with a sequential increase in divergence, starting 110-157 and ending 24-30 Ma. On the basis of the occurrence of Z-linked genes hemizygous in females, we estimate that about one-third of the Z chromosome does not recombine with the W chromosome in female meiosis. Pairwise d(N)/d(S) between gametologs decreased with age, suggesting strong evolutionary constraint in old gametologs. Lineage-specific d(N)/d(S) was consistently higher in W-linked genes, in accordance with the lower efficacy of selection expected in nonrecombining chromosomes. A higher ratio of GC > AT:AT > GC substitutions in W-linked genes supports a role for GC-biased gene conversion in differentially driving base composition on the two sex chromosomes. A male-to-female (M:F) expression ratio of close to one for recombining genes and close to two for Z-linked genes lacking a W copy show that dosage compensation is essentially absent. Some gametologous genes have retained active expression of the W copy in females (giving a M:F ratio of 1 for the gametologous gene pair), whereas for others W expression has become severely reduced resulting in a M:F ratio of close to 2. These observations resemble the patterns of sex chromosome evolution seen in other avian and mammalian lineages, suggesting similar underlying evolutionary processes, although the rate of sex chromosome differentiation has been atypically low. Lack of dosage compensation may be a factor hindering sex chromosome evolution in this lineage.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>24618361</pmid><doi>10.1093/molbev/msu101</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Base Composition biased gene conversion Birds Chromosomes Compensation Dosage Compensation, Genetic Evolution Evolution, Molecular evolutionary strata Female gametologs Gender Gene Conversion Genes Male Mammals Molecular Sequence Data nonrecombining chromosome Recombination, Genetic Sequence Analysis, RNA Sex Chromosomes Struthioniformes - genetics Transcriptome W chromosome Z chromosome |
title | Old but not (so) degenerated--slow evolution of largely homomorphic sex chromosomes in ratites |
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