mRNA和miRNA转录组的联合分析揭示了鹅卵泡选择阶段卵巢细胞生理差异的分子机制。

IF 3.8 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Xinyue Hu, Hengli Xie, Xi Zhang, Yueyue Lin, Shenqiang Hu, Jiwei Hu, Hua He, Liang Li, Hehe Liu, Jiwen Wang
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引用次数: 0

摘要

在禽类中,卵泡选择是决定禽类产蛋量的关键分子事件。卵巢细胞(TC)是卵泡的主要组成部分,但卵巢细胞在卵泡选择阶段的生理差异的分子机制尚不清楚。本研究揭示了天府肉鹅前分层绒毛膜细胞(phTC)和分层绒毛膜细胞(hTC)在增殖、凋亡、脂质合成和类固醇分泌水平上的显著差异。在phTC和hTC之间分别发现了1559个差异表达基因(DEG)和71个差异表达miRNA(DEM)。功能富集分析结果显示,143 个 DEGs 富集在与细胞增殖/凋亡和脂质/类固醇代谢相关的通路中。蛋白质-蛋白质相互作用(PPI)网络结果表明,这143个DEGs具有功能相互作用。此外,71个DEMs的预测靶基因与上述143个DEGs进行了联合分析,结果发现15个DEMs和17个DEGs存在靶向关系。其中,miR-202-5p在hTCs和分级蒂层中均显著下调,靶向预测结果显示,miR-202-5p可能通过靶向CHPT1调控CCN1/FOXO3的表达水平来影响TCs的增殖/凋亡;同时,可能通过靶向CHPT1调控p53/ABCA1/SREBP-2的表达水平来影响TCs的脂质/类固醇代谢和增殖/凋亡。这项研究为了解鹅卵泡选择过程中TCs生理差异的调控机制提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined analyses of mRNA and miRNA transcriptome reveal the molecular mechanisms of theca cells physiological differences in geese follicular selection stage.

In avian, follicular selection is a key molecular event that can determine avian egg production. Theca cells (TC) are the main components of follicles, the molecular mechanisms about TCs physiological differences during follicle selection stage are still unclear. This study revealed significant differences in proliferation, apoptosis, lipid synthesis, and steroid secretion levels between prehierarchical theca cells (phTC) and hierarchical theca cells (hTC) of Tianfu meat-type geese. A total of 1,559 differentially expressed genes (DEG) and 71 differentially expressed miRNAs (DEM) were identified between phTCs and hTCs, respectively. Functional enrichment analysis results showed that 143 DEGs were enriched in the pathways related to cell proliferation/apoptosis and lipid/steroid metabolism. Protein-protein interaction (PPI) network results indicated the 143 DEGs have functional interactions. Additionally, the predicted target genes of 71 DEMs were jointly analyzed with the above 143 DEGs, and the results showed that 15 DEMs and 17 DEGs with targeted relationships were found. Among them, miR-202-5p was significantly down-regulated both in hTCs and hierarchical theca layers, and target prediction results showed that miR-202-5p may affect TCs proliferation/apoptosis by targeting CHPT1 to regulate the expression levels of CCN1/FOXO3; meanwhile, may affect TCs lipid/steroid metabolism and proliferation/apoptosis by targeting CHPT1 to regulate the expression levels of p53/ABCA1/SREBP-2. This study provides new insights into the regulatory mechanisms of TCs physiological differences during goose follicle selection.

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来源期刊
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
期刊介绍: First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers. An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.
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