Integrated data driven analysis identifies potential candidate genes associated with PCOS

IF 2.6 4区 生物学 Q2 BIOLOGY Computational Biology and Chemistry Pub Date : 2024-08-30 DOI:10.1016/j.compbiolchem.2024.108191
Shaini Joseph , Krutika Patil , Niharika Rahate , Jatin Shah , Srabani Mukherjee , Smita D. Mahale
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Abstract

Polycystic ovary syndrome (PCOS) is one of the most common anovulatory disorder observed in women presenting with infertility. Several high and low throughput studies on PCOS have led to accumulation of vast amount of information on PCOS. Despite the availability of several resources which index the advances in PCOS, information on its etiology still remains inadequate. Analysis of the existing information using an integrated evidence based approach may aid identification of novel potential candidate genes with a role in PCOS pathophysiology. This work focuses on integrating existing information on PCOS from literature and gene expression studies and evaluating the application of gene prioritization and network analysis to predict missing novel candidates. Further, it assesses the utility of evidence-based scoring to rank genes for their association with PCOS. The results of this study led to identification of ∼2000 plausible candidate genes associated with PCOS. Insilico validation of these identified candidates confirmed the role of 938 genes in PCOS. Further, experimental validation was carried out for four of the potential candidate genes, a high-scoring (PROS1), two mid-scoring (C1QA and KNG1), and a low-scoring gene (VTN) involved in the complement and coagulation pathway by comparing protein levels in follicular fluid in women with PCOS and healthy controls. While the expression of PROS1, C1QA, and KNG1 was found to be significantly downregulated in women with PCOS, the expression of VTN was found to be unchanged in PCOS. The findings of this study reiterate the utility of employing insilico approaches to identify and prioritize the most promising candidate genes in diseases with a complex pathophysiology like PCOS. Further, the study also helps in gaining clearer insights into the molecular mechanisms associated with the manifestation of the PCOS phenotype by contributing to the existing repertoire of genes associated with PCOS.

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综合数据驱动分析确定了与多囊卵巢综合症相关的潜在候选基因。
多囊卵巢综合征(PCOS)是女性不孕症患者中最常见的无排卵性疾病之一。关于多囊卵巢综合症的多项高通量和低通量研究积累了大量有关多囊卵巢综合症的信息。尽管有一些资料显示了多囊卵巢综合症的进展,但有关其病因的信息仍然不足。采用基于证据的综合方法分析现有信息,有助于发现在多囊卵巢综合症病理生理学中发挥作用的潜在候选基因。这项工作的重点是从文献和基因表达研究中整合有关多囊卵巢综合症的现有信息,并评估基因优先排序和网络分析的应用,以预测缺失的新候选基因。此外,该研究还评估了基于证据的评分法对与多囊卵巢综合症相关的基因进行排序的实用性。研究结果发现了 2000 个与多囊卵巢综合症相关的可信候选基因。对这些已确定的候选基因进行的内部验证确认了 938 个基因在多囊卵巢综合症中的作用。此外,通过比较多囊卵巢综合症妇女和健康对照组卵泡液中的蛋白水平,对四个潜在候选基因进行了实验验证,其中包括一个高分基因(PROS1)、两个中分基因(C1QA 和 KNG1)和一个低分基因(VTN),这些基因涉及补体和凝血途径。结果发现,PROS1、C1QA 和 KNG1 的表达在多囊卵巢综合症女性患者中明显下调,而 VTN 的表达在多囊卵巢综合症患者中却没有变化。这项研究的结果再次证明,在像多囊卵巢综合症这样病理生理学复杂的疾病中,采用非分子方法来鉴定和优先选择最有希望的候选基因是非常有用的。此外,这项研究还有助于更清楚地了解与多囊卵巢综合症表型表现相关的分子机制,为现有的多囊卵巢综合症相关基因库做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Computational Biology and Chemistry
Computational Biology and Chemistry 生物-计算机:跨学科应用
CiteScore
6.10
自引率
3.20%
发文量
142
审稿时长
24 days
期刊介绍: Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered. Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered. Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.
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