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微小RNA-204通过靶向沉默信息调节因子1调控奶山羊精原干细胞增殖

miR-204 Regulates the Proliferation of Dairy Goat Spermatogonial Stem Cells via Targeting to Sirt1.

作者信息

Niu Bowen, Wu Jiang, Mu Hailong, Li Bo, Wu Chongyang, He Xin, Bai Chunling, Li Guangpeng, Hua Jinlian

机构信息

1 College of Veterinary Medicine, Shaanxi Centre of Stem Cells Engineering & Technology, Key Lab for Animal Biotechnology of Agriculture Ministry of China, Northwest A&F University , Yangling, Shaanxi, China .

2 College of Agriculture, Guangdong Ocean University , Zhanjiang, China .

出版信息

Rejuvenation Res. 2016 Apr;19(2):120-30. doi: 10.1089/rej.2015.1719. Epub 2016 Feb 1.

Abstract

The regulation of spermatogonial stem cell (SSC) proliferation and self-renewal is a complex process. Several studies on the microRNA regulation of mammalian spermatogenesis have been reported. Here, we predicted miRNA targeting of Sirt1, and a dual luciferase experiment confirmed that miR-204 interacted with the Sirt1 3'-untranslated region (3'-UTR). The expression of miR-204 and Sirt1 in dairy goat testicles was investigated, and the results showed that the expression pattern of Sirt1 was similar to that of miR-204 in the temporal-spatial distribution. The over-expression of Sirt1 in goat SSCs can promote SSCs' self-renewal gene expression and cell proliferation. Furthermore, miRNA sequencing results showed that Sirt1 had a higher expression level in dairy goat CD49f(+) and CD90(+) SSCs, but the expression level of miR-204 was lower. In an in vitro assay, Sirt1 was significantly down-regulated in dairy goat SSCs when transfected with miR-204 mimics, indicating that Sirt1 was a target of miR-204 in the dairy goat. On the basis of the results of RT-qPCR, fluorescence-activated cell sorting (FACS), and western blotting, we found that the over-expression of Sirt1 in goat SSCs can promote cellular proliferation and change self-renewal and pluripotent gene expression. Thus, miR-204 was involved in the regulation of dairy goat SSCs proliferation via Sirt1.

摘要

精原干细胞(SSC)增殖和自我更新的调控是一个复杂的过程。已有多项关于哺乳动物精子发生的微小RNA调控的研究报道。在此,我们预测了靶向Sirt1的微小RNA,双荧光素酶实验证实miR-204与Sirt1的3'-非翻译区(3'-UTR)相互作用。我们研究了miR-204和Sirt1在奶山羊睾丸中的表达情况,结果表明Sirt1的表达模式在时空分布上与miR-204相似。在山羊精原干细胞中过表达Sirt1可促进精原干细胞自我更新基因的表达和细胞增殖。此外,微小RNA测序结果显示,Sirt1在奶山羊CD49f(+)和CD90(+)精原干细胞中的表达水平较高,但miR-204的表达水平较低。在体外实验中,当用miR-204模拟物转染奶山羊精原干细胞时,Sirt1显著下调,表明Sirt1是奶山羊中miR-204的靶点。基于逆转录-定量聚合酶链反应(RT-qPCR)、荧光激活细胞分选(FACS)和蛋白质印迹法的结果,我们发现山羊精原干细胞中Sirt1的过表达可促进细胞增殖并改变自我更新和多能基因的表达。因此,miR-204通过Sirt1参与了奶山羊精原干细胞增殖的调控。

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