Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure
Background. The bone morphogenetic protein-15 (BMP-15) gene is thought to be one of the important candidate genes involved in premature ovarian failure (POF). However, to date, there has been no consensus on the relationship between mutations in BMP-15 and ovarian dysfunction. Objective. To analyse...
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Veröffentlicht in: | Acta obstetricia et gynecologica Scandinavica 2007-01, Vol.86 (5), p.585-589 |
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description | Background. The bone morphogenetic protein-15 (BMP-15) gene is thought to be one of the important candidate genes involved in premature ovarian failure (POF). However, to date, there has been no consensus on the relationship between mutations in BMP-15 and ovarian dysfunction. Objective. To analyse mutations in the BMP-15 gene in Chinese women with POF. Materials and methods. We sequenced the BMP-15 gene protein coding region of 92 patients and 76 healthy controls that cycle regularly. Results. No mutations were found in the BMP-15 gene protein coding region. There was no difference in the incidence of single nucleotide polymorphism (SNP) rs 17003221 (C→T) in exon 2 (p>0.05), or SNP rs (3810682C→G: ss16336587) in the putative promoter region of exon 1, between the two groups. However, the allele gene frequency in SNP rs (3810682C→G: ss16336587) was C (97.92%) and G (2.08%), respectively, in Chinese women, which is different from other races. Conclusions. Our findings indicate that mutations in BMP-15 exons, or changes in BMP-15 pro-peptide, are rare in Chinese women with POF. In addition, our data suggest that the 2 SNPs are not related to POF in Chinese women, while providing evidence for SNP variation between different races. |
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The bone morphogenetic protein-15 (BMP-15) gene is thought to be one of the important candidate genes involved in premature ovarian failure (POF). However, to date, there has been no consensus on the relationship between mutations in BMP-15 and ovarian dysfunction. Objective. To analyse mutations in the BMP-15 gene in Chinese women with POF. Materials and methods. We sequenced the BMP-15 gene protein coding region of 92 patients and 76 healthy controls that cycle regularly. Results. No mutations were found in the BMP-15 gene protein coding region. There was no difference in the incidence of single nucleotide polymorphism (SNP) rs 17003221 (C→T) in exon 2 (p>0.05), or SNP rs (3810682C→G: ss16336587) in the putative promoter region of exon 1, between the two groups. However, the allele gene frequency in SNP rs (3810682C→G: ss16336587) was C (97.92%) and G (2.08%), respectively, in Chinese women, which is different from other races. Conclusions. Our findings indicate that mutations in BMP-15 exons, or changes in BMP-15 pro-peptide, are rare in Chinese women with POF. In addition, our data suggest that the 2 SNPs are not related to POF in Chinese women, while providing evidence for SNP variation between different races.</description><identifier>ISSN: 0001-6349</identifier><identifier>EISSN: 1600-0412</identifier><identifier>DOI: 10.1080/00016340701269492</identifier><identifier>PMID: 17464588</identifier><identifier>CODEN: AOGSAE</identifier><language>eng</language><publisher>Oxford, UK: Informa UK Ltd</publisher><subject>Asian Continental Ancestry Group - genetics ; Biological and medical sciences ; BMP-15 gene ; Bone Morphogenetic Protein 15 ; Case-Control Studies ; China ; DNA Primers ; exon ; Female ; Genetic Predisposition to Disease ; Growth Differentiation Factor 9 ; Gynecology. Andrology. Obstetrics ; Humans ; Intercellular Signaling Peptides and Proteins - genetics ; Medical sciences ; mutation ; Point Mutation ; Polymerase Chain Reaction ; Premature ovarian failure ; Primary Ovarian Insufficiency - genetics ; SNP</subject><ispartof>Acta obstetricia et gynecologica Scandinavica, 2007-01, Vol.86 (5), p.585-589</ispartof><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><rights>Acta Obstet Gynecol Scand 2007</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5082-68fd10241de6c8af77bc11f12410e37590c43e15406f9d19cbfd6bfe6d86c6a63</citedby><cites>FETCH-LOGICAL-c5082-68fd10241de6c8af77bc11f12410e37590c43e15406f9d19cbfd6bfe6d86c6a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1080%2F00016340701269492$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1080%2F00016340701269492$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18759721$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17464588$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Shi, Yu-Hua</creatorcontrib><creatorcontrib>Wang, Lai-Cheng</creatorcontrib><creatorcontrib>Chen, Zi-Jiang</creatorcontrib><title>Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure</title><title>Acta obstetricia et gynecologica Scandinavica</title><addtitle>Acta Obstet Gynecol Scand</addtitle><description>Background. The bone morphogenetic protein-15 (BMP-15) gene is thought to be one of the important candidate genes involved in premature ovarian failure (POF). However, to date, there has been no consensus on the relationship between mutations in BMP-15 and ovarian dysfunction. Objective. To analyse mutations in the BMP-15 gene in Chinese women with POF. Materials and methods. We sequenced the BMP-15 gene protein coding region of 92 patients and 76 healthy controls that cycle regularly. Results. No mutations were found in the BMP-15 gene protein coding region. There was no difference in the incidence of single nucleotide polymorphism (SNP) rs 17003221 (C→T) in exon 2 (p>0.05), or SNP rs (3810682C→G: ss16336587) in the putative promoter region of exon 1, between the two groups. However, the allele gene frequency in SNP rs (3810682C→G: ss16336587) was C (97.92%) and G (2.08%), respectively, in Chinese women, which is different from other races. Conclusions. Our findings indicate that mutations in BMP-15 exons, or changes in BMP-15 pro-peptide, are rare in Chinese women with POF. In addition, our data suggest that the 2 SNPs are not related to POF in Chinese women, while providing evidence for SNP variation between different races.</description><subject>Asian Continental Ancestry Group - genetics</subject><subject>Biological and medical sciences</subject><subject>BMP-15 gene</subject><subject>Bone Morphogenetic Protein 15</subject><subject>Case-Control Studies</subject><subject>China</subject><subject>DNA Primers</subject><subject>exon</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Growth Differentiation Factor 9</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - genetics</subject><subject>Medical sciences</subject><subject>mutation</subject><subject>Point Mutation</subject><subject>Polymerase Chain Reaction</subject><subject>Premature ovarian failure</subject><subject>Primary Ovarian Insufficiency - genetics</subject><subject>SNP</subject><issn>0001-6349</issn><issn>1600-0412</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhB3BBvsAt4Ekc2xGnsoIFqVA-tYiL8Tpj4jYfi53Q9t_jVSJ6QIKTNZ7nnfH7mpCHwJ4CU-wZYwxEwZlkkIuKV_ktsgLBWMY45LfJ6tDPElAdkXsxnqcql1zdJUcgueClUivy_RP-nLC3SH-Z4E0_Rup7ildDH-ng6NggffH2fQYl_YE9HnrrxvcYke7N6PHAX_qxofuAnRmngHSYB1FnfJvq--SOM23EB8t5TL68evl5_To7Pdu8WZ-cZrZkKs-EcjWwnEONwirjpNxZAAfphmEhy4pZXiCUnAlX1VDZnavFzqGolbDCiOKYPJnn7sOQHMVRdz5abFvT4zBFLRkvQCqWQJhBG4YYAzq9D74z4VoD04dY9V-xJs2jZfi067C-USw5JuDxAphoTeuC6a2PN5xKDmQOiStn7tK3eP3_zfrkbDM_IJt1Po549UdnwoUWMsWjt-82ertlXwE-ftDfEv984Xs3hM40aNqxsSagPh-m0Kef-Ifd36gNr1s</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Zhang, Peng</creator><creator>Shi, Yu-Hua</creator><creator>Wang, Lai-Cheng</creator><creator>Chen, Zi-Jiang</creator><general>Informa UK Ltd</general><general>Blackwell Publishing Ltd</general><general>Taylor & Francis</general><scope>BSCLL</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>20070101</creationdate><title>Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure</title><author>Zhang, Peng ; Shi, Yu-Hua ; Wang, Lai-Cheng ; Chen, Zi-Jiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5082-68fd10241de6c8af77bc11f12410e37590c43e15406f9d19cbfd6bfe6d86c6a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Asian Continental Ancestry Group - genetics</topic><topic>Biological and medical sciences</topic><topic>BMP-15 gene</topic><topic>Bone Morphogenetic Protein 15</topic><topic>Case-Control Studies</topic><topic>China</topic><topic>DNA Primers</topic><topic>exon</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Growth Differentiation Factor 9</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - genetics</topic><topic>Medical sciences</topic><topic>mutation</topic><topic>Point Mutation</topic><topic>Polymerase Chain Reaction</topic><topic>Premature ovarian failure</topic><topic>Primary Ovarian Insufficiency - genetics</topic><topic>SNP</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Shi, Yu-Hua</creatorcontrib><creatorcontrib>Wang, Lai-Cheng</creatorcontrib><creatorcontrib>Chen, Zi-Jiang</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Acta obstetricia et gynecologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Peng</au><au>Shi, Yu-Hua</au><au>Wang, Lai-Cheng</au><au>Chen, Zi-Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure</atitle><jtitle>Acta obstetricia et gynecologica Scandinavica</jtitle><addtitle>Acta Obstet Gynecol Scand</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>86</volume><issue>5</issue><spage>585</spage><epage>589</epage><pages>585-589</pages><issn>0001-6349</issn><eissn>1600-0412</eissn><coden>AOGSAE</coden><abstract>Background. The bone morphogenetic protein-15 (BMP-15) gene is thought to be one of the important candidate genes involved in premature ovarian failure (POF). However, to date, there has been no consensus on the relationship between mutations in BMP-15 and ovarian dysfunction. Objective. To analyse mutations in the BMP-15 gene in Chinese women with POF. Materials and methods. We sequenced the BMP-15 gene protein coding region of 92 patients and 76 healthy controls that cycle regularly. Results. No mutations were found in the BMP-15 gene protein coding region. There was no difference in the incidence of single nucleotide polymorphism (SNP) rs 17003221 (C→T) in exon 2 (p>0.05), or SNP rs (3810682C→G: ss16336587) in the putative promoter region of exon 1, between the two groups. However, the allele gene frequency in SNP rs (3810682C→G: ss16336587) was C (97.92%) and G (2.08%), respectively, in Chinese women, which is different from other races. Conclusions. Our findings indicate that mutations in BMP-15 exons, or changes in BMP-15 pro-peptide, are rare in Chinese women with POF. In addition, our data suggest that the 2 SNPs are not related to POF in Chinese women, while providing evidence for SNP variation between different races.</abstract><cop>Oxford, UK</cop><pub>Informa UK Ltd</pub><pmid>17464588</pmid><doi>10.1080/00016340701269492</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Asian Continental Ancestry Group - genetics Biological and medical sciences BMP-15 gene Bone Morphogenetic Protein 15 Case-Control Studies China DNA Primers exon Female Genetic Predisposition to Disease Growth Differentiation Factor 9 Gynecology. Andrology. Obstetrics Humans Intercellular Signaling Peptides and Proteins - genetics Medical sciences mutation Point Mutation Polymerase Chain Reaction Premature ovarian failure Primary Ovarian Insufficiency - genetics SNP |
title | Sequence variants in exons of the BMP-15 gene in Chinese patients with premature ovarian failure |
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