标题:Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency
作者:Luo W.; Guo T.; Li G.; Liu R.; Zhao S.; Song M.; Zhang L.; Wang S.;等 更多
作者机构:[Luo, W] Center for Reproductive Medicine, Shandong University. National Research Center for Assisted Reproductive Technology and Reproductive Genetic 更多
来源:The Journal of clinical endocrinology and metabolism
出版年:2020
卷:105
期:10
DOI:10.1210/clinem/dgaa505
关键词:POI; DNA repair; EXO1; RAD51; whole exome sequencing
摘要:CONTEXT: Premature ovarian insufficiency (POI) is characterized by cessation of menstruation before 40 years of age and elevated serum level of FSH (>25 IU/L). Recent studies have found a few causative genes responsible for POI enriched in meiotic recombination and DNA damage repair pathways. OBJECTIVE: To investigate the role of variations in homologous recombination genes played in POI pathogenesis. METHODS: The whole exome sequencing was performed in 50 POI patients with primary amenorrhea. Functional characterizations of the novel variants were carried out in budding yeast and human cell line. RESULTS: We identified 8 missense variants in 7 homologous recombination genes, including EXO1, RAD51, RMI1, MSH5, MSH2, MSH6, and MLH1. The mutation p.Thr52Ser in EXO1 impaired the meiotic process of budding yeast and p.Glu68Gly in RAD51-altered protein localization in human cells, both of them impaired the efficiency of homologous recombination repair for DNA double-stranded breaks in human cells. CONCLUSIONS: Our study first linked the variants of EXO1 and RAD51 with POI and further highlighted the role of DNA repair genes in ovarian dysgenesis. © Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
收录类别:SCOPUS
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090492000&doi=10.1210%2fclinem%2fdgaa505&partnerID=40&md5=5e8b2a07babfb4aec108d04941608b9e
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