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环状RNA-长链间核糖核酸-长链非编码RNA-微小RNA-信使核糖核酸竞争性内源RNA调控网络的构建鉴定了与山羊繁殖力相关的基因和通路。

Construction of a circRNA- lincRNA-lncRNA-miRNA-mRNA ceRNA regulatory network identifies genes and pathways linked to goat fertility.

作者信息

Ghafouri Farzad, Sadeghi Mostafa, Bahrami Abolfazl, Naserkheil Masoumeh, Dehghanian Reyhan Vahid, Javanmard Arash, Miraei-Ashtiani Seyed Reza, Ghahremani Soheila, Barkema Herman W, Abdollahi-Arpanahi Rostam, Kastelic John P

机构信息

Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran.

Biomedical Center for Systems Biology Science Munich, Ludwig-Maximilians-University, Munich, Germany.

出版信息

Front Genet. 2023 Jul 21;14:1195480. doi: 10.3389/fgene.2023.1195480. eCollection 2023.

Abstract

There is growing interest in the genetic improvement of fertility traits in female goats. With high-throughput genotyping, single-cell RNA sequencing (scRNA-seq) is a powerful tool for measuring gene expression profiles. The primary objective was to investigate comparative transcriptome profiling of granulosa cells (GCs) of high- and low-fertility goats, using scRNA-seq. Thirty samples from Ji'ning Gray goats ( = 15 for high fertility and = 15 for low fertility) were retrieved from publicly available scRNA-seq data. Functional enrichment analysis and a literature mining approach were applied to explore modules and hub genes related to fertility. Then, interactions between types of RNAs identified were predicted, and the ceRNA regulatory network was constructed by integrating these interactions with other gene regulatory networks (GRNs). Comparative transcriptomics-related analyses identified 150 differentially expressed genes (DEGs) between high- and low-fertility groups, based on the fold change (≥5 and ≤-5) and false discovery rate (FDR <0.05). Among these genes, 80 were upregulated and 70 were downregulated. In addition, 81 mRNAs, 58 circRNAs, 8 lincRNAs, 19 lncRNAs, and 55 miRNAs were identified by literature mining. Furthermore, we identified 18 hub genes (, , , , , , , , , , , , , , , , , and ) involved in goat fertility. Identified biological networks and modules were mainly associated with ovary signature pathways. In addition, KEGG enrichment analysis identified regulating pluripotency of stem cells, cytokine-cytokine receptor interactions, ovarian steroidogenesis, oocyte meiosis, progesterone-mediated oocyte maturation, parathyroid and growth hormone synthesis, cortisol synthesis and secretion, and signaling pathways for prolactin, TGF-beta, Hippo, MAPK, PI3K-Akt, and FoxO. Functional annotation of identified DEGs implicated important biological pathways. These findings provided insights into the genetic basis of fertility in female goats and are an impetus to elucidate molecular ceRNA regulatory networks and functions of DEGs underlying ovarian follicular development.

摘要

人们对雌性山羊繁殖性状的遗传改良越来越感兴趣。借助高通量基因分型,单细胞RNA测序(scRNA-seq)是测量基因表达谱的强大工具。主要目的是利用scRNA-seq研究高繁殖力和低繁殖力山羊颗粒细胞(GCs)的比较转录组图谱。从公开的scRNA-seq数据中获取了30个来自济宁青山羊的样本(高繁殖力15个,低繁殖力15个)。应用功能富集分析和文献挖掘方法来探索与繁殖力相关的模块和枢纽基因。然后,预测所鉴定的RNA类型之间的相互作用,并通过将这些相互作用与其他基因调控网络(GRNs)整合来构建ceRNA调控网络。基于倍数变化(≥5和≤-5)和错误发现率(FDR<0.05),比较转录组学相关分析在高繁殖力和低繁殖力组之间鉴定出150个差异表达基因(DEGs)。其中,80个上调,70个下调。此外,通过文献挖掘鉴定出81个mRNA、58个环状RNA、8个长链非编码RNA(lincRNA)、19个长链非编码RNA(lncRNA)和55个miRNA。此外,我们鉴定出18个参与山羊繁殖力的枢纽基因(、、、、、、、、、、、、、、、、和)。鉴定出的生物网络和模块主要与卵巢特征途径相关。此外,KEGG富集分析确定了干细胞多能性调控、细胞因子-细胞因子受体相互作用、卵巢类固醇生成、卵母细胞减数分裂、孕酮介导的卵母细胞成熟、甲状旁腺和生长激素合成、皮质醇合成和分泌以及催乳素、TGF-β、Hippo、MAPK、PI3K-Akt和FoxO的信号通路。所鉴定的DEGs的功能注释涉及重要的生物学途径。这些发现为雌性山羊繁殖力的遗传基础提供了见解,并推动阐明卵巢卵泡发育潜在的分子ceRNA调控网络和DEGs的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615c/10400778/66d1791b2d4e/fgene-14-1195480-g001.jpg

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