The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
Human oocyte maturation is a precondition for fertilization and ensuing embryonic development. Previously, we identified TUBB8 variants as a genetic determinant of human oocyte maturation arrest and showed that these variants cause variable and mixed phenotypes in oocyte maturation and early embryo...
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Veröffentlicht in: | European journal of human genetics : EJHG 2019-02, Vol.27 (2), p.300-307 |
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creator | Chen, Biaobang Wang, Wenjing Peng, Xiandong Jiang, Huafeng Zhang, Shaozhen Li, Da Li, Bin Fu, Jing Kuang, Yanping Sun, Xiaoxi Wang, Xueqian Zhang, Zhihua Wu, Ling Zhou, Zhou Lyu, Qifeng Yan, Zheng Mao, Xiaoyan Xu, Yao Mu, Jian Li, Qiaoli Jin, Li He, Lin Sang, Qing Wang, Lei |
description | Human oocyte maturation is a precondition for fertilization and ensuing embryonic development. Previously, we identified TUBB8 variants as a genetic determinant of human oocyte maturation arrest and showed that these variants cause variable and mixed phenotypes in oocyte maturation and early embryo development. We also estimated that rare inherited or de novo variants in the TUBB8 gene accounted for 30% of individuals in a small cohort of patients affected by oocyte maturation arrest. In the present study, we recruited a further 87 patients from unrelated families diagnosed with oocyte maturation or early embryonic arrest and identified 30 patients carrying TUBB8 variants. The corresponding phenotypes not only include oocyte maturation arrest, failure of fertilization, and early embryonic arrest, but also extend to the new phenotype of failure of embryo implantation. These observations provide the most detailed mutational and phenotypic spectrum of TUBB8, further extend the spectrum of variants and dysfunctional oocyte and embryo phenotypes caused by TUBB8 variants, and confirm previous findings for a critical role of TUBB8 during oocyte maturation and early embryonic development. Thus, TUBB8 mutation screening might not only be a genetic diagnostic marker for patients with oocyte maturation arrest, but might also have clinical implications for evaluating the competence of patients' functional oocytes with first polar body (PB1). |
doi_str_mv | 10.1038/s41431-018-0283-3 |
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Previously, we identified TUBB8 variants as a genetic determinant of human oocyte maturation arrest and showed that these variants cause variable and mixed phenotypes in oocyte maturation and early embryo development. We also estimated that rare inherited or de novo variants in the TUBB8 gene accounted for 30% of individuals in a small cohort of patients affected by oocyte maturation arrest. In the present study, we recruited a further 87 patients from unrelated families diagnosed with oocyte maturation or early embryonic arrest and identified 30 patients carrying TUBB8 variants. The corresponding phenotypes not only include oocyte maturation arrest, failure of fertilization, and early embryonic arrest, but also extend to the new phenotype of failure of embryo implantation. These observations provide the most detailed mutational and phenotypic spectrum of TUBB8, further extend the spectrum of variants and dysfunctional oocyte and embryo phenotypes caused by TUBB8 variants, and confirm previous findings for a critical role of TUBB8 during oocyte maturation and early embryonic development. Thus, TUBB8 mutation screening might not only be a genetic diagnostic marker for patients with oocyte maturation arrest, but might also have clinical implications for evaluating the competence of patients' functional oocytes with first polar body (PB1).</description><identifier>ISSN: 1018-4813</identifier><identifier>EISSN: 1476-5438</identifier><identifier>DOI: 10.1038/s41431-018-0283-3</identifier><identifier>PMID: 30297906</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Adult ; Embryo Implantation ; Embryogenesis ; Female ; Fertilization ; Humans ; Infertility ; Infertility, Female - genetics ; Infertility, Female - pathology ; Mutation ; Oocytes ; Oogenesis ; Phenotype ; Phenotypes ; Tubulin - genetics</subject><ispartof>European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.300-307</ispartof><rights>Copyright Nature Publishing Group Feb 2019</rights><rights>European Society of Human Genetics 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-58df37d427c19d9853bef804458746b8b5e607880f3f565661a89d5d05ea50c63</citedby><cites>FETCH-LOGICAL-c427t-58df37d427c19d9853bef804458746b8b5e607880f3f565661a89d5d05ea50c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336793/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336793/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30297906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Biaobang</creatorcontrib><creatorcontrib>Wang, Wenjing</creatorcontrib><creatorcontrib>Peng, Xiandong</creatorcontrib><creatorcontrib>Jiang, Huafeng</creatorcontrib><creatorcontrib>Zhang, Shaozhen</creatorcontrib><creatorcontrib>Li, Da</creatorcontrib><creatorcontrib>Li, Bin</creatorcontrib><creatorcontrib>Fu, Jing</creatorcontrib><creatorcontrib>Kuang, Yanping</creatorcontrib><creatorcontrib>Sun, Xiaoxi</creatorcontrib><creatorcontrib>Wang, Xueqian</creatorcontrib><creatorcontrib>Zhang, Zhihua</creatorcontrib><creatorcontrib>Wu, Ling</creatorcontrib><creatorcontrib>Zhou, Zhou</creatorcontrib><creatorcontrib>Lyu, Qifeng</creatorcontrib><creatorcontrib>Yan, Zheng</creatorcontrib><creatorcontrib>Mao, Xiaoyan</creatorcontrib><creatorcontrib>Xu, Yao</creatorcontrib><creatorcontrib>Mu, Jian</creatorcontrib><creatorcontrib>Li, Qiaoli</creatorcontrib><creatorcontrib>Jin, Li</creatorcontrib><creatorcontrib>He, Lin</creatorcontrib><creatorcontrib>Sang, Qing</creatorcontrib><creatorcontrib>Wang, Lei</creatorcontrib><title>The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility</title><title>European journal of human genetics : EJHG</title><addtitle>Eur J Hum Genet</addtitle><description>Human oocyte maturation is a precondition for fertilization and ensuing embryonic development. Previously, we identified TUBB8 variants as a genetic determinant of human oocyte maturation arrest and showed that these variants cause variable and mixed phenotypes in oocyte maturation and early embryo development. We also estimated that rare inherited or de novo variants in the TUBB8 gene accounted for 30% of individuals in a small cohort of patients affected by oocyte maturation arrest. In the present study, we recruited a further 87 patients from unrelated families diagnosed with oocyte maturation or early embryonic arrest and identified 30 patients carrying TUBB8 variants. The corresponding phenotypes not only include oocyte maturation arrest, failure of fertilization, and early embryonic arrest, but also extend to the new phenotype of failure of embryo implantation. These observations provide the most detailed mutational and phenotypic spectrum of TUBB8, further extend the spectrum of variants and dysfunctional oocyte and embryo phenotypes caused by TUBB8 variants, and confirm previous findings for a critical role of TUBB8 during oocyte maturation and early embryonic development. Thus, TUBB8 mutation screening might not only be a genetic diagnostic marker for patients with oocyte maturation arrest, but might also have clinical implications for evaluating the competence of patients' functional oocytes with first polar body (PB1).</description><subject>Adult</subject><subject>Embryo Implantation</subject><subject>Embryogenesis</subject><subject>Female</subject><subject>Fertilization</subject><subject>Humans</subject><subject>Infertility</subject><subject>Infertility, Female - genetics</subject><subject>Infertility, Female - pathology</subject><subject>Mutation</subject><subject>Oocytes</subject><subject>Oogenesis</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Tubulin - genetics</subject><issn>1018-4813</issn><issn>1476-5438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</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>eNpdkU1LHTEYhUNRqtX-ADcl4MbNtMnN52yEKvYDBBde1yE386Y3MjOZJhnh_nszXBXbVQ455z28yYPQGSVfKWH6W-aUM9oQqhuy0qxhH9Ax5Uo2gjN9UPXicE3ZEfqU8yMh1VT0IzpiZNWqlshjdL_eAnZxmBJsYczhCfAwF1tCHG2P7djhqd7HspuCw3kCV9I84Ojx-uHqSuMwYg-D7aEqD6mEPpTdKTr0ts_w-eU8QQ8_btbXv5rbu5-_r7_fNo6vVGmE7jxTXdWOtl2rBduA14RzoRWXG70RIInSmnjmhRRSUqvbTnREgBXESXaCLve907wZoHMwlmR7M6Uw2LQz0QbzrzOGrfkTn4xkTKqW1YKLl4IU_86QixlCdtD3doQ4Z7OiVDHNKKc1ev5f9DHOqf7RkpKacqH0Ukj3KZdizgn82zKUmAWZ2SMzFYxZkJll5sv7V7xNvDJizz5rkaQ</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Chen, Biaobang</creator><creator>Wang, Wenjing</creator><creator>Peng, Xiandong</creator><creator>Jiang, Huafeng</creator><creator>Zhang, Shaozhen</creator><creator>Li, Da</creator><creator>Li, Bin</creator><creator>Fu, Jing</creator><creator>Kuang, Yanping</creator><creator>Sun, Xiaoxi</creator><creator>Wang, Xueqian</creator><creator>Zhang, Zhihua</creator><creator>Wu, Ling</creator><creator>Zhou, Zhou</creator><creator>Lyu, Qifeng</creator><creator>Yan, Zheng</creator><creator>Mao, Xiaoyan</creator><creator>Xu, Yao</creator><creator>Mu, Jian</creator><creator>Li, Qiaoli</creator><creator>Jin, Li</creator><creator>He, Lin</creator><creator>Sang, Qing</creator><creator>Wang, Lei</creator><general>Nature Publishing Group</general><general>Springer International Publishing</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>3V.</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190201</creationdate><title>The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility</title><author>Chen, Biaobang ; Wang, Wenjing ; Peng, Xiandong ; Jiang, Huafeng ; Zhang, Shaozhen ; Li, Da ; Li, Bin ; Fu, Jing ; Kuang, Yanping ; Sun, Xiaoxi ; Wang, Xueqian ; Zhang, Zhihua ; Wu, Ling ; Zhou, Zhou ; Lyu, Qifeng ; Yan, Zheng ; Mao, Xiaoyan ; Xu, Yao ; Mu, Jian ; Li, Qiaoli ; Jin, Li ; He, Lin ; Sang, Qing ; Wang, Lei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-58df37d427c19d9853bef804458746b8b5e607880f3f565661a89d5d05ea50c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Embryo Implantation</topic><topic>Embryogenesis</topic><topic>Female</topic><topic>Fertilization</topic><topic>Humans</topic><topic>Infertility</topic><topic>Infertility, Female - genetics</topic><topic>Infertility, Female - pathology</topic><topic>Mutation</topic><topic>Oocytes</topic><topic>Oogenesis</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Tubulin - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Biaobang</creatorcontrib><creatorcontrib>Wang, Wenjing</creatorcontrib><creatorcontrib>Peng, Xiandong</creatorcontrib><creatorcontrib>Jiang, Huafeng</creatorcontrib><creatorcontrib>Zhang, Shaozhen</creatorcontrib><creatorcontrib>Li, Da</creatorcontrib><creatorcontrib>Li, Bin</creatorcontrib><creatorcontrib>Fu, Jing</creatorcontrib><creatorcontrib>Kuang, Yanping</creatorcontrib><creatorcontrib>Sun, Xiaoxi</creatorcontrib><creatorcontrib>Wang, Xueqian</creatorcontrib><creatorcontrib>Zhang, Zhihua</creatorcontrib><creatorcontrib>Wu, Ling</creatorcontrib><creatorcontrib>Zhou, Zhou</creatorcontrib><creatorcontrib>Lyu, Qifeng</creatorcontrib><creatorcontrib>Yan, Zheng</creatorcontrib><creatorcontrib>Mao, Xiaoyan</creatorcontrib><creatorcontrib>Xu, Yao</creatorcontrib><creatorcontrib>Mu, Jian</creatorcontrib><creatorcontrib>Li, Qiaoli</creatorcontrib><creatorcontrib>Jin, Li</creatorcontrib><creatorcontrib>He, Lin</creatorcontrib><creatorcontrib>Sang, Qing</creatorcontrib><creatorcontrib>Wang, Lei</creatorcontrib><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>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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of human genetics : EJHG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Biaobang</au><au>Wang, Wenjing</au><au>Peng, Xiandong</au><au>Jiang, Huafeng</au><au>Zhang, Shaozhen</au><au>Li, Da</au><au>Li, Bin</au><au>Fu, Jing</au><au>Kuang, Yanping</au><au>Sun, Xiaoxi</au><au>Wang, Xueqian</au><au>Zhang, Zhihua</au><au>Wu, Ling</au><au>Zhou, Zhou</au><au>Lyu, Qifeng</au><au>Yan, Zheng</au><au>Mao, Xiaoyan</au><au>Xu, Yao</au><au>Mu, Jian</au><au>Li, Qiaoli</au><au>Jin, Li</au><au>He, Lin</au><au>Sang, Qing</au><au>Wang, Lei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility</atitle><jtitle>European journal of human genetics : EJHG</jtitle><addtitle>Eur J Hum Genet</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>27</volume><issue>2</issue><spage>300</spage><epage>307</epage><pages>300-307</pages><issn>1018-4813</issn><eissn>1476-5438</eissn><abstract>Human oocyte maturation is a precondition for fertilization and ensuing embryonic development. Previously, we identified TUBB8 variants as a genetic determinant of human oocyte maturation arrest and showed that these variants cause variable and mixed phenotypes in oocyte maturation and early embryo development. We also estimated that rare inherited or de novo variants in the TUBB8 gene accounted for 30% of individuals in a small cohort of patients affected by oocyte maturation arrest. In the present study, we recruited a further 87 patients from unrelated families diagnosed with oocyte maturation or early embryonic arrest and identified 30 patients carrying TUBB8 variants. The corresponding phenotypes not only include oocyte maturation arrest, failure of fertilization, and early embryonic arrest, but also extend to the new phenotype of failure of embryo implantation. These observations provide the most detailed mutational and phenotypic spectrum of TUBB8, further extend the spectrum of variants and dysfunctional oocyte and embryo phenotypes caused by TUBB8 variants, and confirm previous findings for a critical role of TUBB8 during oocyte maturation and early embryonic development. Thus, TUBB8 mutation screening might not only be a genetic diagnostic marker for patients with oocyte maturation arrest, but might also have clinical implications for evaluating the competence of patients' functional oocytes with first polar body (PB1).</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>30297906</pmid><doi>10.1038/s41431-018-0283-3</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Embryo Implantation Embryogenesis Female Fertilization Humans Infertility Infertility, Female - genetics Infertility, Female - pathology Mutation Oocytes Oogenesis Phenotype Phenotypes Tubulin - genetics |
title | The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility |
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