Yao Xiaolei, Gao XiaoXiao, Bao Yongjin, El-Samahy M A, Yang Jinyu, Wang Zhibo, Li Xiaodan, Zhang Guomin, Zhang Yanli, Liu Wujun, Wang Feng
Jiangsu Livestock Embryo Engineering Laboratory, Nanjing Agricultural University, Nanjing 210095, China.
Hu Sheep Academy, Nanjing Agricultural University, Nanjing 210095, China.
Mol Ther Nucleic Acids. 2021 Mar 1;24:223-240. doi: 10.1016/j.omtn.2021.02.030. eCollection 2021 Jun 4.
Long non-coding RNAs (lncRNAs) regulate the development of follicles and reproductive diseases, but the mechanisms by which lncRNAs regulate ovarian functions and fertility remain elusive. We profiled the expression of lncRNAs in ovarian tissues of Hu sheep with different prolificacy and identified 21,327 lncRNAs. Many of the lncRNAs were differentially expressed in different groups. We further characterized an lncRNA that was predominantly expressed in the ovaries of the low prolificacy Fec (LPB+) group and mainly present in granulosa cells (GCs), and the expression of this lncRNA decreased during follicular development, which we named follicular development-associated lncRNA (). Next, we found that directly binds miR-543-3p, and decorin () was identified as a target of miR-543-3p. overexpression promoted GC apoptosis through increased expression of , which could be attenuated by miR-543-3p. Furthermore, miR-543-3p increased and reduced the expression of transforming growth factor-β (TGF-β) pathway-related genes, including and inhibin beta A (), which were upregulated upon silencing. Our results demonstrated that sponges miR-543-3p in GCs and prevents miR-543-3p from binding to the 3' UTR, resulting in transactivation and TGF-β pathway inhibition and promotion of GC apoptosis in Hu sheep. These findings provide insights into the mechanisms underlying prolificacy in sheep.
长链非编码RNA(lncRNAs)调节卵泡发育和生殖疾病,但lncRNAs调节卵巢功能和生育能力的机制仍不清楚。我们分析了不同繁殖力的湖羊卵巢组织中lncRNAs的表达,鉴定出21327个lncRNAs。许多lncRNAs在不同组中差异表达。我们进一步鉴定了一种lncRNA,它主要在低繁殖力Fec(LPB+)组的卵巢中表达,主要存在于颗粒细胞(GCs)中,并且在卵泡发育过程中该lncRNA的表达下降,我们将其命名为卵泡发育相关lncRNA()。接下来,我们发现 直接结合miR-543-3p,并且核心蛋白聚糖()被鉴定为miR-543-3p的靶标。 的过表达通过增加 的表达促进GC凋亡,而miR-543-3p可减弱这种促进作用。此外,miR-543-3p增加而 减少转化生长因子-β(TGF-β)途径相关基因的表达,包括 和抑制素βA(),在 沉默后这些基因上调。我们的结果表明, 在GCs中充当miR-543-3p的海绵,阻止miR-543-3p与 的3'UTR结合,导致 反式激活和TGF-β途径抑制,并促进湖羊GC凋亡。这些发现为绵羊繁殖力的潜在机制提供了见解。