Expression profiling and function analysis identified new genes regulating cumulus expansion and cumulus cell apoptosis in mouse oocytes.

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2024-08-02 Print Date: 2024-09-01 DOI:10.1530/REP-24-0128
Min Zhang, Jia-Shun Wu, Xiao Han, Rui-Jie Ma, Jia-Li Xu, Ming-Tao Xu, Hong-Jie Yuan, Ming-Jiu Luo, Jing-He Tan
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Abstract

In brief: Genes expressed in cumulus cells might be used as markers for competent oocytes/embryos. This study identified and validated a new group of cumulus expansion and/or apoptosis-regulating genes, which may be used for selection of quality oocytes/embryos.

Abstract: Studies on the mechanisms behind cumulus expansion and cumulus cell (CC) apoptosis are essential for understanding the mechanisms for oocyte maturation. Genes expressed in CCs might be used as markers for competent oocytes and/or embryos. In this study, both in vitro (IVT) and in vivo (IVO) mouse oocyte models with significant difference in cumulus expansion and CC apoptosis were used to identify and validate new genes regulating cumulus expansion and CC apoptosis of mouse oocytes. We first performed mRNA sequencing and bioinformatic analysis using the IVT oocyte model to identify candidate genes. We then analyzed functions of the candidate genes by RNAi or gene overexpression to select the candidate cumulus expansion and CC apoptosis-regulating genes. Finally, we validated the cumulus expansion and CC apoptosis-regulating genes using the IVO oocyte model. The results showed that while Spp1, Sdc1, Ldlr, Ezr and Mmp2 promoted, Bmp2, Angpt2, Edn1, Itgb8, Cxcl10 and Agt inhibited cumulus expansion. Furthermore, Spp1, Sdc1 and Ldlr inhibited CC apoptosis. In conclusion, by using both IVT and IVO oocyte models, we have identified and validated a new group of cumulus expansion and/or apoptosis-regulating genes, which may be used for selection of quality oocytes/embryos and for elucidating the molecular mechanisms behind oocyte maturation.

表达谱分析和功能分析发现了调节积聚体扩张和凋亡的新基因。
研究积层细胞(CC)扩增和凋亡背后的机制对于了解卵母细胞成熟机制至关重要。CC中表达的基因可用作合格卵母细胞和/或胚胎的标记。在本研究中,我们使用了在体外(IVT)和体内(IVO)两种小鼠卵母细胞模型,这两种模型的卵母细胞在积聚体扩增和CC凋亡方面存在显著差异,我们利用这两种模型来鉴定和验证调控小鼠卵母细胞积聚体扩增和CC凋亡的新基因。我们首先利用 IVT 卵母细胞模型进行了 mRNA 测序和生物信息学分析,以确定候选基因。然后,我们通过 RNAi 或基因过表达分析了候选基因的功能,筛选出了候选的积聚扩增和 CC 凋亡调控基因。最后,我们利用IVO卵母细胞模型验证了积聚扩增和CC凋亡调控基因。结果表明,Spp1、Sdc1、Ldlr、Ezr 和 Mmp2 能促进积聚体扩张,而 Bmp2、Angpt2、Edn1、Itgb8、Cxcl10 和 Agt 则抑制积聚体扩张。此外,Spp1、Sdc1 和 Ldlr 可抑制 CC 的凋亡。总之,通过使用IVT和IVO卵母细胞模型,我们发现并验证了一组新的积聚体扩增和/或凋亡调控基因,这些基因可用于筛选优质卵母细胞/胚胎以及阐明卵母细胞成熟背后的分子机制。
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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
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