Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven
Mammalian evolution is believed to be male driven because the greater number of germ cell divisions per generation in males increases the opportunity for errors in DNA replication. Since the Y Chromosome (Chr) replicates exclusively in males, its genes should also evolve faster than X or autosomal g...
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description | Mammalian evolution is believed to be male driven because the greater number of germ cell divisions per generation in males increases the opportunity for errors in DNA replication. Since the Y Chromosome (Chr) replicates exclusively in males, its genes should also evolve faster than X or autosomal genes. In addition, estimating the overall male-to-female mutation ratio (αₘ) is of great importance as a large αₘ implies that replication-independent mutagenic events play a relatively small role in evolution. A small αₘ suggests that the impact of these factors may, in fact, be significant. In order to address this problem, we have analyzed the rates of evolution in the homologous X-Y common SMCX/SMCY genes from three different species—mouse, human, and horse. The SMC genes were chosen because the X and Y copies are highly homologous, well conserved in evolution, and in all probability functionally interchangeable. Sequence comparisons and analysis of synonymous substitutions in approximately 1kb of the 5′ coding region of the SMC genes reveal that the Y-linked copies are evolving approximately 1.8 times faster than their X homologs. The male-to-female mutation ratio αₘ was estimated to be 3. These data support the hypothesis that mammalian evolution is male driven. However, the ratio value is far smaller than suggested in earlier works, implying significance of replication-independent mutagenic events in evolution. |
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Since the Y Chromosome (Chr) replicates exclusively in males, its genes should also evolve faster than X or autosomal genes. In addition, estimating the overall male-to-female mutation ratio (αₘ) is of great importance as a large αₘ implies that replication-independent mutagenic events play a relatively small role in evolution. A small αₘ suggests that the impact of these factors may, in fact, be significant. In order to address this problem, we have analyzed the rates of evolution in the homologous X-Y common SMCX/SMCY genes from three different species—mouse, human, and horse. The SMC genes were chosen because the X and Y copies are highly homologous, well conserved in evolution, and in all probability functionally interchangeable. Sequence comparisons and analysis of synonymous substitutions in approximately 1kb of the 5′ coding region of the SMC genes reveal that the Y-linked copies are evolving approximately 1.8 times faster than their X homologs. The male-to-female mutation ratio αₘ was estimated to be 3. These data support the hypothesis that mammalian evolution is male driven. However, the ratio value is far smaller than suggested in earlier works, implying significance of replication-independent mutagenic events in evolution.</description><identifier>ISSN: 0938-8990</identifier><identifier>EISSN: 1432-1777</identifier><identifier>DOI: 10.1007/s003359900372</identifier><identifier>PMID: 9060413</identifier><language>eng</language><publisher>United States: Springer-Verlag</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Conserved sequence ; DNA biosynthesis ; DNA, Complementary ; Evolution ; Evolution, Molecular ; Evolutionary genetics ; Histone Demethylases ; Histone-Lysine N-Methyltransferase ; Horses ; Humans ; Male ; Males ; Mice ; Minor Histocompatibility Antigens ; Molecular Sequence Data ; Mutation ; Mutation rates ; Oxidoreductases, N-Demethylating ; Proteins - genetics ; Replication ; Sequence Homology, Amino Acid ; Sex Characteristics ; X Chromosome ; Y Chromosome</subject><ispartof>Mammalian genome, 1997-02, Vol.8 (2), p.134-138</ispartof><rights>Springer-Verlag 1997.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-48d785d9fd379610d6a8692f1df3941665fe864d88bab7c4f1a839f104b562723</citedby><cites>FETCH-LOGICAL-c402t-48d785d9fd379610d6a8692f1df3941665fe864d88bab7c4f1a839f104b562723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9060413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Agulnik, A I</creatorcontrib><creatorcontrib>Bishop, C E</creatorcontrib><creatorcontrib>Lerner, J L</creatorcontrib><creatorcontrib>Agulnik, S I</creatorcontrib><creatorcontrib>Solovyev, V V</creatorcontrib><title>Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven</title><title>Mammalian genome</title><addtitle>Mamm Genome</addtitle><description>Mammalian evolution is believed to be male driven because the greater number of germ cell divisions per generation in males increases the opportunity for errors in DNA replication. Since the Y Chromosome (Chr) replicates exclusively in males, its genes should also evolve faster than X or autosomal genes. In addition, estimating the overall male-to-female mutation ratio (αₘ) is of great importance as a large αₘ implies that replication-independent mutagenic events play a relatively small role in evolution. A small αₘ suggests that the impact of these factors may, in fact, be significant. In order to address this problem, we have analyzed the rates of evolution in the homologous X-Y common SMCX/SMCY genes from three different species—mouse, human, and horse. The SMC genes were chosen because the X and Y copies are highly homologous, well conserved in evolution, and in all probability functionally interchangeable. Sequence comparisons and analysis of synonymous substitutions in approximately 1kb of the 5′ coding region of the SMC genes reveal that the Y-linked copies are evolving approximately 1.8 times faster than their X homologs. The male-to-female mutation ratio αₘ was estimated to be 3. These data support the hypothesis that mammalian evolution is male driven. However, the ratio value is far smaller than suggested in earlier works, implying significance of replication-independent mutagenic events in evolution.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Conserved sequence</subject><subject>DNA biosynthesis</subject><subject>DNA, Complementary</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Evolutionary genetics</subject><subject>Histone Demethylases</subject><subject>Histone-Lysine N-Methyltransferase</subject><subject>Horses</subject><subject>Humans</subject><subject>Male</subject><subject>Males</subject><subject>Mice</subject><subject>Minor Histocompatibility Antigens</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Mutation rates</subject><subject>Oxidoreductases, N-Demethylating</subject><subject>Proteins - genetics</subject><subject>Replication</subject><subject>Sequence Homology, Amino Acid</subject><subject>Sex Characteristics</subject><subject>X Chromosome</subject><subject>Y Chromosome</subject><issn>0938-8990</issn><issn>1432-1777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUtLAzEUhYMotVaXLsXgQlejeT-WpfiCigsVdBXSTlJHZiaazCj990ZbBF24uRfu-e5ZnAPAPkanGCF5lhCilGudlyQbYIgZJQWWUm6CIdJUFSpr22AnpReEsBRYDsBAI4EYpkNgxq2tl6lKMHjY9J3tqtDCaDuXYNXC7tnBu5vJ01kej3Dh2nxOz-EjZcV2sLFNY-vKttC9h7r__s1W-eZgGat31-6CLW_r5PbWewQeLs7vJ1fF9PbyejKeFnOGSFcwVUrFS-1LKrXAqBRWCU08Lj3VDAvBvVOClUrN7EzOmcdWUe0xYjMuiCR0BE5Wvq8xvPUudaap0tzVtW1d6JNRXEjBFGWZPP6XxFyznCXK4NEf8CX0MceVjNRES05zvCNQrKB5DClF581rrBoblwYj89WP-dVP5g_Wpv2sceUPvS4k64cr3dtg7CJWyTzcEYRF7o5yrgn9BOjakZU</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>Agulnik, A I</creator><creator>Bishop, C E</creator><creator>Lerner, J L</creator><creator>Agulnik, S I</creator><creator>Solovyev, V V</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</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>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope></search><sort><creationdate>19970201</creationdate><title>Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven</title><author>Agulnik, A I ; Bishop, C E ; Lerner, J L ; Agulnik, S I ; Solovyev, V V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-48d785d9fd379610d6a8692f1df3941665fe864d88bab7c4f1a839f104b562723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Conserved sequence</topic><topic>DNA biosynthesis</topic><topic>DNA, Complementary</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Evolutionary genetics</topic><topic>Histone Demethylases</topic><topic>Histone-Lysine N-Methyltransferase</topic><topic>Horses</topic><topic>Humans</topic><topic>Male</topic><topic>Males</topic><topic>Mice</topic><topic>Minor Histocompatibility Antigens</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Mutation rates</topic><topic>Oxidoreductases, N-Demethylating</topic><topic>Proteins - genetics</topic><topic>Replication</topic><topic>Sequence Homology, Amino Acid</topic><topic>Sex Characteristics</topic><topic>X Chromosome</topic><topic>Y Chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agulnik, A I</creatorcontrib><creatorcontrib>Bishop, C E</creatorcontrib><creatorcontrib>Lerner, J L</creatorcontrib><creatorcontrib>Agulnik, S I</creatorcontrib><creatorcontrib>Solovyev, V V</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech 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 Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</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 Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><jtitle>Mammalian genome</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agulnik, A I</au><au>Bishop, C E</au><au>Lerner, J L</au><au>Agulnik, S I</au><au>Solovyev, V V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven</atitle><jtitle>Mammalian genome</jtitle><addtitle>Mamm Genome</addtitle><date>1997-02-01</date><risdate>1997</risdate><volume>8</volume><issue>2</issue><spage>134</spage><epage>138</epage><pages>134-138</pages><issn>0938-8990</issn><eissn>1432-1777</eissn><abstract>Mammalian evolution is believed to be male driven because the greater number of germ cell divisions per generation in males increases the opportunity for errors in DNA replication. Since the Y Chromosome (Chr) replicates exclusively in males, its genes should also evolve faster than X or autosomal genes. In addition, estimating the overall male-to-female mutation ratio (αₘ) is of great importance as a large αₘ implies that replication-independent mutagenic events play a relatively small role in evolution. A small αₘ suggests that the impact of these factors may, in fact, be significant. In order to address this problem, we have analyzed the rates of evolution in the homologous X-Y common SMCX/SMCY genes from three different species—mouse, human, and horse. The SMC genes were chosen because the X and Y copies are highly homologous, well conserved in evolution, and in all probability functionally interchangeable. Sequence comparisons and analysis of synonymous substitutions in approximately 1kb of the 5′ coding region of the SMC genes reveal that the Y-linked copies are evolving approximately 1.8 times faster than their X homologs. The male-to-female mutation ratio αₘ was estimated to be 3. These data support the hypothesis that mammalian evolution is male driven. However, the ratio value is far smaller than suggested in earlier works, implying significance of replication-independent mutagenic events in evolution.</abstract><cop>United States</cop><pub>Springer-Verlag</pub><pmid>9060413</pmid><doi>10.1007/s003359900372</doi><tpages>5</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Conserved sequence DNA biosynthesis DNA, Complementary Evolution Evolution, Molecular Evolutionary genetics Histone Demethylases Histone-Lysine N-Methyltransferase Horses Humans Male Males Mice Minor Histocompatibility Antigens Molecular Sequence Data Mutation Mutation rates Oxidoreductases, N-Demethylating Proteins - genetics Replication Sequence Homology, Amino Acid Sex Characteristics X Chromosome Y Chromosome |
title | Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven |
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