MiRNA novel-216 regulated fatty acid composition and progesterone synthesis in goat granulosa cells by targeting TPD52.

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2024-11-01 DOI:10.1530/REP-24-0231
Yuhang Jia, Qiao Xu, Peng Wang, Ziyi Liu, Runan Zhang, Kai Liu, Yinghui Ling, Yufang Liu, Xing Ming Chu
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Abstract

Granulosa cells in the ovaries of livestock are crucial for secreting steroid hormones that regulate follicular development, with lipid synthesis and metabolism playing key roles in this process. The molecular mechanisms behind steroid hormone secretion regulated by fatty acid metabolism in goat granulosa cells have been unclear. Our previous transcriptome analysis of Yunshang black goat ovaries revealed that miR-novel-216, which had lower expression in high-fertility goats, might regulate granulosa cell function. We further investigated the role of miR-novel-216 by isolating and culturing goat granulosa cells in vitro, and found that it inhibits cell proliferation, lipid accumulation, and progesterone synthesis in goat granulosa cells. The qTar and miRanda analyses predicted TPD52 as a target of miR-novel-216, confirmed by dual luciferase and transfection assays. Previous studies have shown that progesterone synthesis in granulosa cells is closely related to free fatty acid composition. We investigated the effect of in vitro construction of TPD52 overexpression and interference plasmids on the free fatty acid content of goat granulosa cells using mass spectrometry sequencing. The results showed that overexpression of TPD52 in goat granulosa cells significantly increased free fatty acid content and promoted granulosa cell proliferation, lipid accumulation, and progesterone synthesis, whereas the opposite was true for inhibition of TPD52. It was shown that miR-novel-216 affects granulosa cell proliferation and free fatty acid levels by regulating the expression of TPD52, which increases reproductive hormone secretion and promotes polytocous trait in goats. This provides a foundation for developing breeding strategies to improve goat fertility.

MiRNA novel-216 通过靶向 TPD52 调节山羊颗粒细胞的脂肪酸组成和孕酮合成。
家畜卵巢中的颗粒细胞是分泌调节卵泡发育的类固醇激素的关键,而脂质的合成和代谢在这一过程中起着关键作用。脂肪酸代谢调节山羊颗粒细胞分泌类固醇激素的分子机制尚不清楚。我们之前对云山黑山羊卵巢的转录组分析表明,在高繁殖力山羊中表达较低的 miR-novel-216 可能会调控颗粒细胞的功能。我们通过分离和体外培养山羊颗粒细胞,进一步研究了 miR-novel-216 的作用,发现它能抑制山羊颗粒细胞的增殖、脂质积累和孕酮合成。qTar和miRanda分析预测TPD52是miR-novel-216的靶标,并通过双荧光素酶和转染试验证实了这一点。以前的研究表明,颗粒细胞中孕酮的合成与游离脂肪酸的组成密切相关。我们利用质谱测序法研究了体外构建TPD52过表达质粒和干扰质粒对山羊颗粒细胞游离脂肪酸含量的影响。结果表明,在山羊颗粒细胞中过表达 TPD52 能显著增加游离脂肪酸含量,促进颗粒细胞增殖、脂质积累和孕酮合成,而抑制 TPD52 则相反。研究表明,miR-novel-216 通过调节 TPD52 的表达影响颗粒细胞增殖和游离脂肪酸含量,从而增加生殖激素分泌,促进山羊的多胎性状。这为制定提高山羊繁殖力的育种策略奠定了基础。
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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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