miR‐31 Regulates Spermatogonial Stem Cells Meiosis via Targeting Stra8

减数分裂 生物 转染 小RNA 细胞生物学 流式细胞术 干细胞 基因 遗传学
作者
Yingjie Wang,Qisheng Zuo,Yulin Bi,Wenhui Zhang,Jing Jin,Liangliang Zhang,Ya‐ni Zhang,Bichun Li
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:118 (12): 4844-4853 被引量:19
标识
DOI:10.1002/jcb.26159
摘要

ABSTRACT Stra8 (stimulated by retinoic acid gene 8) is a specific gene that is expressed in mammalian germ cells during transition from mitosis to meiosis and plays a key role in the initiation of meiosis in mammals and birds. So, the evaluation of the Stra8 pathway in cSSCs may provide a deeper insight into mammalian spermatogenesis. miRNA was also an important regulating factor for meiosis of SSCs. However, there is currently no data indicating that miRNA regulate the meiosis of SSCs via Stra8. Here, we predicted the prospective miRNA targeting to Stra8 using the online Bioinformatics database‐Targetscan, and performed an analysis of the dual‐luciferase recombinant vector, pGL3‐CMV‐LUC‐MCS‐Stra8‐3′UTR. miR‐31 mimics (miR‐31m), miR‐31 inhibitors (miR‐31i), Control (NC, scrambled oligonucleotides transfection) were transfected into cSSCs; Stra8 and miRNA were analyzed by RT‐qPCR, immunofluorescence, and Western blot. The detection of haploid was conducted by flow cytometry. The results showed that miR‐31 regulates meiosis of cSSCs via targeting Stra8 in vitro and in vivo. Our study identifies a new regulatory pathway that miR‐31 targets Stra8 and inhibits spermatogenesis. J. Cell. Biochem. 118: 4844–4853, 2017. © 2017 Wiley Periodicals, Inc.
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