SEMA4G targeted by miR-363-5p regulates the proliferation of granulosa cells in Yunshang black goats

Yulin Chen, Peng Wang, Xiaoyun He, Yufang Liu, Mingxing Chu
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Abstract

Proliferation of granular cells (GCs) plays an important role in ovary development, providing energy and a microenvironment for oocyte ovulation. In this study, we explored the spatiotemporal expression of SEMA4G and its effects on the growth and development of goat GCs using primary GCs cultured in vitro as a model. The results showed that the expression level of SEMA4G was significantly higher in the ovaries of high-fertility goats than in those of low-fertility goats (p < 0.05). The mRNA and protein expression levels of the cell proliferation markers of GCs were significantly increased after the overexpression of SEMA4G in goat primary GCs. The EdU and CCK8 results showed that cell viability was elevated in goat GCs and that proliferation was promoted by an increase in the number of proliferating cells. The proliferation of goat GCs was significantly inhibited by SEMA4G inhibition (p < 0.05). The results of online miRNA and target gene prediction software and dual luciferase activity analysis confirmed that SEMA4G could bind to mi-363-5p and was one of its target genes. The RT‒qPCR results showed that the expression level of miR-363-5p was significantly lower in the ovaries of high-fertility goats than in those of low-fertility goats in contrast to the expression level of SEMA4G (p < 0.05). After the overexpression of miR-363-5p in goat GCs, the expression of SEMA4G was significantly suppressed (p < 0.05). Collectively, the results of this study could lay the foundation for exploring the molecular mechanisms by which SEMA4G and miR-363-5p regulate the growth and development of goat GCs and provide targets for breeding high-fertility goats.

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miR-363-5p靶向的SEMA4G调控云山黑山羊颗粒细胞的增殖
颗粒细胞(GCs)的增殖在卵巢发育中起着重要作用,它为卵母细胞排卵提供能量和微环境。本研究以体外培养的原代GCs为模型,探讨了SEMA4G的时空表达及其对山羊GCs生长发育的影响。结果表明,SEMA4G在高繁殖力山羊卵巢中的表达水平明显高于低繁殖力山羊(p <0.05)。在山羊原代GCs中过表达SEMA4G后,GCs细胞增殖标志物的mRNA和蛋白表达水平明显升高。EdU和CCK8结果表明,山羊GCs细胞活力提高,增殖细胞数量增加,促进了细胞增殖。抑制 SEMA4G 能显著抑制山羊 GCs 的增殖(p < 0.05)。在线 miRNA 和靶基因预测软件及双荧光素酶活性分析结果证实,SEMA4G 可与 mi-363-5p 结合,是其靶基因之一。RT-qPCR结果显示,高繁殖力山羊卵巢中miR-363-5p的表达水平明显低于低繁殖力山羊卵巢中SEMA4G的表达水平(p <0.05)。在山羊GC中过表达miR-363-5p后,SEMA4G的表达被显著抑制(p <0.05)。总之,本研究的结果可为探索SEMA4G和miR-363-5p调控山羊GCs生长发育的分子机制奠定基础,并为培育高繁殖力山羊提供靶标。
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