Department of Histology and Embryology, School of Medicine, Yangzhou University, Yangzhou, China.
Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou University, Yangzhou, China.
J Cell Mol Med. 2020 Apr;24(7):4194-4211. doi: 10.1111/jcmm.15080. Epub 2020 Feb 24.
STRA8 (Stimulated By Retinoic Acid Gene 8) is a retinoic acid (RA) induced gene that plays vital roles in spermatogonial proliferation, differentiation and meiosis. The SETD8 and STRA8 protein interaction was discovered using the yeast two-hybrid technique using a mouse spermatogonial stem cell (SSC) cDNA library. The interaction of these two proteins was confirmed using co-immunoprecipitation and identification of key domains governing the protein: protein complex. STRA8 and SETD8 showed a mutual transcriptional regulation pattern that provided evidence that SETD8 negatively regulated transcriptional activity of the STRA8 promoter. The SETD8 protein directly bound to the proximal promoter of the STRA8 gene. STRA8 increased the transcriptional activity of SETD8 promoter in a dose-dependent manner. For the first time, we have discovered that STRA8 and SETD8 display a cell cycle-dependent expression pattern in germline cells. Expression levels of SETD8 and H4K20me1 in S phase of STRA8 overexpression GC1 cells were different from that previously observed in tumour cell lines. In wild-type mice testis, SETD8, H4K20me1 and PCNA co-localized with STRA8 in spermatogonia. Further, our studies quantitated abnormal expression levels of cell cycle and ubiquitination-related factors in STRA8 dynamic models. STRA8 and SETD8 may regulate spermatogenesis via Cdl4-Clu4A-Ddb1 ubiquitinated degradation axis in a PCNA-dependent manner.
STRA8(视黄酸诱导基因 8)是一种视黄酸(RA)诱导基因,在精原细胞增殖、分化和减数分裂中发挥重要作用。使用酵母双杂交技术,从小鼠精原干细胞(SSC)cDNA 文库中发现了 SETD8 和 STRA8 蛋白之间的相互作用。通过共免疫沉淀和鉴定控制蛋白-蛋白复合物的关键结构域,证实了这两种蛋白质之间的相互作用。STRA8 和 SETD8 表现出相互转录调节模式,这为 SETD8 负调控 STRA8 启动子转录活性提供了证据。SETD8 蛋白直接结合到 STRA8 基因的近端启动子上。STRA8 以剂量依赖的方式增加 SETD8 启动子的转录活性。我们首次发现 STRA8 和 SETD8 在生殖细胞中表现出细胞周期依赖性表达模式。在 STRA8 过表达 GC1 细胞的 S 期,SETD8 和 H4K20me1 的表达水平与以前在肿瘤细胞系中观察到的不同。在野生型小鼠睾丸中,SETD8、H4K20me1 和 PCNA 与 STRA8 在精原细胞中共定位。此外,我们的研究还定量分析了 STRA8 动态模型中细胞周期和泛素化相关因子的异常表达水平。STRA8 和 SETD8 可能通过 PCNA 依赖性方式调节 Cdl4-Clu4A-Ddb1 泛素化降解轴来调节精子发生。