The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China, Collaborative Innovation Center of Genetics and Development, Hefei 230027, China.
The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China, Collaborative Innovation Center of Genetics and Development, Hefei 230027, China.
Genomics Proteomics Bioinformatics. 2022 Jun;20(3):455-465. doi: 10.1016/j.gpb.2021.08.010. Epub 2021 Dec 24.
Exploring the genetic basis of human infertility is currently under intensive investigation. However, only a handful of genes have been validated in animal models as disease-causing genes in infertile men. Thus, to better understand the genetic basis of human spermatogenesis and bridge the knowledge gap between humans and other animal species, we construct the FertilityOnline, a database integrating the literature-curated functional genes during spermatogenesis into an existing spermatogenic database, SpermatogenesisOnline 1.0. Additional features, including the functional annotation and genetic variants of human genes, are also incorporated into FertilityOnline. By searching this database, users can browse the functional genes involved in spermatogenesis and instantly narrow down the number of candidates of genetic mutations underlying male infertility in a user-friendly web interface. Clinical application of this database was exampled by the identification of novel causative mutations in synaptonemal complex central element protein 1 (SYCE1) and stromal antigen 3 (STAG3) in azoospermic men. In conclusion, FertilityOnline is not only an integrated resource for spermatogenic genes but also a useful tool facilitating the exploration of the genetic basis of male infertility. FertilityOnline can be freely accessed at http://mcg.ustc.edu.cn/bsc/spermgenes2.0/index.html.
目前,人们正在深入研究人类不育症的遗传基础。然而,只有少数几个基因在动物模型中被验证为男性不育症的致病基因。因此,为了更好地了解人类精子发生的遗传基础,并弥合人类和其他动物物种之间的知识差距,我们构建了 FertilityOnline,这是一个将精子发生过程中文献整理的功能基因整合到现有的精子发生数据库 SpermatogenesisOnline 1.0 中的数据库。该数据库还整合了人类基因的功能注释和遗传变异等额外功能。通过搜索这个数据库,用户可以浏览参与精子发生的功能基因,并通过用户友好的网络界面立即缩小导致男性不育遗传突变的候选基因数量。该数据库的临床应用实例是在无精子症男性中鉴定出联会复合体中央元件蛋白 1 (SYCE1) 和基质抗原 3 (STAG3) 的新的致病突变。总之,FertilityOnline 不仅是一个整合的精子发生基因资源,也是一个有助于探索男性不育症遗传基础的有用工具。该数据库可在 http://mcg.ustc.edu.cn/bsc/spermgenes2.0/index.html 免费访问。