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男性不育知识库:解码遗传与疾病图谱。

Male Infertility Knowledgebase: decoding the genetic and disease landscape.

机构信息

Genetic Research Center, ICMR-National Institute for Research in Reproductive Health, J.M. Street, Parel, Mumbai 400012, India.

Emeritus Scientist, ICMR-National Institute for Research in Reproductive Health, J.M. Street, Parel, Mumbai 400012, India.

出版信息

Database (Oxford). 2021 Aug 7;2021. doi: 10.1093/database/baab049.

Abstract

Male infertility is a multifactorial condition that contributes to around one-third of cases of infertility worldwide. Several chromosomal aberrations, single-gene and polygenic associations with male factor defects have been reported. These defects manifest as sperm number or sperm quality defects leading to infertility. However, in almost 40% of cases, the genetic etiology of male infertility remains unexplained. Understanding the causal genetic factors is crucial for effective patient management and counseling. Integrating the vast amount of available omics data on male infertility is a first step towards understanding, delineating and prioritizing genes associated with the different male reproductive disorders. The Male Infertility Knowledgebase (MIK) is a manually curated repository developed to boost research on the elusive genetic etiology of male infertility. It integrates information on ∼17 000 genes, their associated pathways, gene ontology, diseases and gene and sequence-based analysis tools. In addition, it also incorporates information on reported chromosomal aberrations and syndromic associations with male infertility. Disease enrichment of genes in MIK indicate a shared genetic etiology between cancer, male and female infertility disorders. While the genes involved in cancer pathways were found to be common causal factors for sperm number and sperm quality defects, the interleukin pathways were found to be shared and enriched between male factor defects and non-reproductive conditions like cardiovascular diseases, metabolic diseases, etc. Disease information in MIK can be explored further to identify high-risk conditions associated with male infertility and delineate shared genetic etiology. Utility of the knowledgebase in predicting novel genes is illustrated by identification of 149 novel candidates for cryptorchidism using gene prioritization and network analysis. MIK will serve as a platform for review of genetic information on male infertility, identification pleiotropic genes, prediction of novel candidate genes for the different male infertility diseases and for portending future high-risk diseases associated with male infertility. Database URL: http://mik.bicnirrh.res.in/.

摘要

男性不育是一种多因素病症,约占全球不育病例的三分之一。已经报道了几种染色体异常、单基因和多基因与男性因素缺陷的关联。这些缺陷表现为精子数量或质量缺陷,导致不育。然而,在近 40%的情况下,男性不育的遗传病因仍未得到解释。了解因果遗传因素对于有效的患者管理和咨询至关重要。整合大量可用的男性不育症组学数据是理解、描绘和优先考虑与不同男性生殖障碍相关基因的第一步。男性不育知识库(MIK)是一个手动策展的存储库,旨在促进对男性不育难以捉摸的遗传病因的研究。它整合了约 17000 个基因及其相关途径、基因本体论、疾病和基于基因和序列的分析工具的信息。此外,它还包含了与男性不育相关的染色体异常和综合征关联的信息。MIK 中基因的疾病富集表明癌症、男性和女性不育症之间存在共同的遗传病因。虽然参与癌症途径的基因被发现是精子数量和质量缺陷的常见因果因素,但白细胞介素途径在男性因素缺陷和非生殖疾病(如心血管疾病、代谢疾病等)之间被发现是共同的和富集的。MIK 中的疾病信息可以进一步探索,以识别与男性不育相关的高风险情况,并描绘共同的遗传病因。通过基因优先级排序和网络分析,使用知识库来预测 149 个新的隐睾候选基因,说明了知识库在预测新基因方面的效用。MIK 将作为审查男性不育遗传信息、识别多效基因、预测不同男性不育疾病的新候选基因以及预示与男性不育相关的未来高风险疾病的平台。数据库 URL:http://mik.bicnirrh.res.in/。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aaa/8346693/e60457f1592e/baab049f1.jpg

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