甲基体蛋白 50 是青鳉卵子发生的必要条件

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2024-02-28 DOI:10.1016/j.cbd.2024.101220
Qiting Yao , Qing Yang , Zhenyu Li , Fan Wu , Shi Duan , Mengxi Cao , Xinhua Chen , Xueping Zhong , Qingchun Zhou , Haobin Zhao
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引用次数: 0

摘要

甲基组蛋白 50(Mep50)是精氨酸甲基转移酶 5 的伙伴。Mep50 是人类雄激素受体和雌激素受体的辅助激活剂。Mep50 在果蝇生殖细胞的发育过程中起着至关重要的作用。在脊椎动物中,Mep50在卵子发生中的确切作用仍不清楚。本研究旨在探讨Mep50在青鳉卵子发生过程中的作用。干扰Mep50会导致青鳉的卵子发生受损,并形成多个卵母细胞滤泡。RNA-seq分析显示,突变体卵巢中的基因表达存在显著差异,4542个基因上调,1264个基因下调。受调控的基因主要集中在细胞基质和ECM-受体相互作用、Notch信号通路、PI3K-Akt信号通路、MAPK信号通路、Hippo信号通路和Jak-Stat通路等。此外,与下丘脑-垂体-性腺轴、类固醇代谢和 IGF 系统相关的基因也受到了影响。此外,mep50的突变导致卵巢细胞中前mRNA的替代剪接发生了显著变化。定量 RT-PCR 结果验证了 RNA-seq 分析在特定基因(包括 akt2、map3k5、yap1、fshr、cyp17a、igf1、ythdc2、cdk6 和 col1 等)中的发现。这项研究结果表明,Mep50 在卵子发生过程中发挥着至关重要的作用,参与了类固醇代谢、细胞基质调控和信号通路等多种生物过程。这可能是通过调控青鳉卵巢细胞中 mRNA 的剪接来实现的。
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Methylosome protein 50 is necessary for oogenesis in medaka

Methylosome protein 50 (Mep50) functions as a partner to protein arginine methyltransferase 5. MEP50 serves as a coactivator for both the androgen receptor and estrogen receptor in humans. Mep50 plays a crucial role in the development of germ cells in Drosophila. The precise role of Mep50 in oogenesis remains unclear in vertebrates. The objective of this study was to investigate the role of Mep50 in oogenesis in medaka fish. Disruption of Mep50 resulted in impaired oogenesis and the formation of multiple oocyte follicles in medaka. RNA-seq analysis revealed significant differential gene expression in the mutant ovary, with 4542 genes up-regulated and 1264 genes down-regulated. The regulated genes were found to be enriched in cellular matrices and ECM-receptor interaction, the Notch signaling pathway, the PI3K-Akt signaling pathway, the MAPK signaling pathway, the Hippo signaling pathway, and the Jak-Stat pathway, among others. In addition, the genes related to the hypothalamus-pituitary-gonad axis, steroid metabolism, and IGF system were impacted. Furthermore, the mutation of mep50 caused significant alterations in alternative splicing of pre-mRNA in ovarian cells. Quantitative RT-PCR results validated the findings from RNA-seq analysis in the specific genes, including akt2, map3k5, yap1, fshr, cyp17a, igf1, ythdc2, cdk6, and col1, among others. The findings of this study demonstrate that Mep50 plays a crucial role in oogenesis, participating in a diverse range of biological processes such as steroid metabolism, cell matrix regulation, and signal pathways. This may be achieved through the regulation of gene expression via mRNA splicing in medaka ovarian cells.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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