细胞生长
多囊卵巢
小RNA
生物
分子生物学
细胞凋亡
细胞周期蛋白D1
逆转录聚合酶链式反应
卵巢
信使核糖核酸
细胞计数
实时聚合酶链反应
报告基因
细胞周期
内分泌学
基因表达
基因
遗传学
胰岛素抵抗
胰岛素
作者
Yufang Liu,Yulin Chen,Zuyang Zhou,Xiaoyun He,Lin Tao,Yanting Jiang,Lan Rong,Qionghua Hong,Mingxing Chu
标识
DOI:10.3389/fvets.2021.732440
摘要
Granulosa cell (GC) proliferation provides essential conditions for ovulation in animals. A previous study showed that DENND1A plays a significant role in polycystic ovary syndrome. However, the modulation of DENND1A in GCs remains unclear. Our previous integrated analysis of miRNA-mRNA revealed that the 3'-untranslated region of DENND1A could be a target of chi-miR-324-3p. In this study, we used quantitative reverse transcription polymerase chain reaction (RT-qPCR) to investigate DENND1A expression in ovarian tissues of high- and low-yielding goats. Furthermore, dual-fluorescent reporter vector experiments, Cell Counting Kit-8 (CCK-8) assay, and RT-qPCR were used to elucidate the regulatory pathway of chi-miR-324-3p-DENND1A in GCs. The results revealed an opposite tendency between the expressions of chi-miR-324-3p and DENND1A in the ovaries of high- and low-yielding goats. The CCK-8 assay indicated that chi-miR-324-3p overexpression significantly suppressed GC proliferation, whereas chi-miR-324-3p inhibition promoted GC proliferation. In addition, the expressions of GC proliferation markers LHR, Cylin D2, and CDK4 showed the same tendency. The dual-fluorescent reporter assay revealed that chi-miR-324-3p directly targeted DENND1A, and the RT-qPCR results revealed that DENND1A expression was inhibited by chi-miR-324-3p. In summary, chi-miR-324-3p inhibited the proliferation of GCs by targeting DENND1A.
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