Wang Yingjie, Zuo Qisheng, Bi Yulin, Zhang Wenhui, Jin Jing, Zhang Liangliang, Zhang Ya-Ni, Li Bichun
College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, Jiangsu Province, P.R. China.
Key Laboratory for Animal Genetics, Breeding, Reproduction, and Molecular Design of Jiangsu Province, Yangzhou, 225009, Jiangsu Province, P.R. China.
J Cell Biochem. 2017 Dec;118(12):4844-4853. doi: 10.1002/jcb.26159. Epub 2017 Jun 20.
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.
Stra8(视黄酸刺激基因8)是一种特异性基因,在哺乳动物生殖细胞从有丝分裂向减数分裂转变过程中表达,在哺乳动物和鸟类减数分裂起始过程中起关键作用。因此,评估cSSCs中Stra8信号通路可能有助于更深入了解哺乳动物精子发生过程。miRNA也是精原干细胞减数分裂的重要调节因子。然而,目前尚无数据表明miRNA通过Stra8调节精原干细胞的减数分裂。在此,我们使用在线生物信息学数据库Targetscan预测了靶向Stra8的潜在miRNA,并对双荧光素酶重组载体pGL3-CMV-LUC-MCS-Stra8-3'UTR进行了分析。将miR-31模拟物(miR-31m)、miR-31抑制剂(miR-31i)、对照(NC,乱序寡核苷酸转染)转染到cSSCs中;通过RT-qPCR、免疫荧光和蛋白质印迹分析Stra8和miRNA。通过流式细胞术检测单倍体。结果表明,miR-31在体外和体内均通过靶向Stra8调节cSSCs的减数分裂。我们的研究确定了一条新的调控途径,即miR-31靶向Stra8并抑制精子发生。《细胞生物化学杂志》2017年第118卷:4844 - 4853页。©2017威利期刊公司