In silico exploring of the epigenetic factors in teratozoospermia: A focus on IGF2BP2.

IF 1 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Seyedeh Zahra Mousavi, Bahram Mohammad-Soltani, Morteza Hadizadeh, Zeynab Rokhsattalab, Mehdi Totonchi
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引用次数: 0

Abstract

Teratozoospermia is an abnormal sperm morphology that is a common cause of male infertility. Epigenetic factors have been implicated in the regulation of gene expression in teratozoospermia, but the specific mechanisms are not fully understood. This study aimed to identify differentially expressed genes (DEGs) between teratozoospermia and normozoospermia samples, and to investigate the role of epigenetic regulatory factors in the observed gene expression changes. The study integrated data from three publicly available datasets in the GSE6969 superseries. The DEGs were compared to a list of known human epigenetic-related genes obtained from the EpiFactors database. The protein-protein interaction (PPI) network and hub gene identifications for Epi-DEGs and the RNA-protein interaction (RPI) network to obtained the RBPs interacting with Epi-DEGs were constructed. siRNA design for the candidate mRNA was performed using various bioinformatics tools. As a result, the obtained 1,292 DEGs were compared to a list of 796 known human epigenetic factors, revealing 63 Epi-DEGs. The PPI network of Epi-DEGs identified top 10 hub genes including RBBP7, HDAC2, EZH2, SMARCA5, SUV39H1, CTCF, DNMT1, MORF4L1, ARID4B and KDM5B. The RPI network analysis revealed IGF2BP2, SFPQ and A1CF as key RNA-binding protein regulators epigenetic modifiers. Based on these findings, the study designed the sequence GCAACAAGAGAAGAA GCAATT as an optimal siRNA candidate targeting the master regulator IGF2BP2, which exhibited the most significant change in expression among the RNA-binding proteins (RBPs). This integrative analysis sheds light on the epigenetic mechanisms underlying teratozoospermia and highlights the potential of RBPs as diagnostic biomarkers and therapeutic targets for further investigation.

畸形精子症表观遗传因素的芯片探索:以IGF2BP2为重点。
畸形精子症是一种精子形态异常,是男性不育的常见原因。表观遗传因素参与了畸形精子症基因表达的调控,但具体机制尚不完全清楚。本研究旨在鉴定畸形精子症和正常精子症样本之间的差异表达基因(DEGs),并探讨表观遗传调控因子在观察到的基因表达变化中的作用。该研究整合了GSE6969超级系列中三个公开可用数据集的数据。将deg与从EpiFactors数据库中获得的已知人类表观遗传相关基因列表进行比较。构建了Epi-DEGs的蛋白-蛋白相互作用(PPI)网络和枢纽基因鉴定,以及获得与Epi-DEGs相互作用的rbp的rna -蛋白相互作用(RPI)网络。候选mRNA的siRNA设计使用各种生物信息学工具进行。结果,将获得的1292个DEGs与已知的796个人类表观遗传因子列表进行比较,发现63个Epi-DEGs。Epi-DEGs的PPI网络鉴定出前10个枢纽基因,包括RBBP7、HDAC2、EZH2、SMARCA5、SUV39H1、CTCF、DNMT1、MORF4L1、ARID4B和KDM5B。RPI网络分析显示IGF2BP2、SFPQ和A1CF是关键的rna结合蛋白调控因子。基于这些发现,本研究设计了GCAACAAGAGAAGAA GCAATT序列,作为在rna结合蛋白(rbp)中表达变化最显著的主调控因子IGF2BP2的最佳siRNA候选序列。这项综合分析揭示了畸形精子症的表观遗传机制,并强调了rbp作为诊断生物标志物和治疗靶点的潜力,值得进一步研究。
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
Molecular Biology Research Communications
Molecular Biology Research Communications BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.00
自引率
0.00%
发文量
12
期刊介绍: “Molecular Biology Research Communications” (MBRC) is an international journal of Molecular Biology. It is published quarterly by Shiraz University (Iran). The MBRC is a fully peer-reviewed journal. The journal welcomes submission of Original articles, Short communications, Invited review articles, and Letters to the Editor which meets the general criteria of significance and scientific excellence in all fields of “Molecular Biology”.
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