Fong Yick W, Ho Jaclyn J, Inouye Carla, Tjian Robert
Department of Molecular and Cell Biology, Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, United States.
Elife. 2014 Nov 19;3:e03573. doi: 10.7554/eLife.03573.
Acquisition of pluripotency is driven largely at the transcriptional level by activators OCT4, SOX2, and NANOG that must in turn cooperate with diverse coactivators to execute stem cell-specific gene expression programs. Using a biochemically defined in vitro transcription system that mediates OCT4/SOX2 and coactivator-dependent transcription of the gene, we report the purification and identification of the dyskerin (DKC1) ribonucleoprotein complex as an OCT4/SOX2 coactivator whose activity appears to be modulated by a subset of associated small nucleolar RNAs (snoRNAs). The DKC1 complex occupies enhancers and regulates the expression of key pluripotency genes critical for self-renewal in embryonic stem (ES) cells. Depletion of DKC1 in fibroblasts significantly decreased the efficiency of induced pluripotent stem (iPS) cell generation. This study thus reveals an unanticipated transcriptional role of the DKC1 complex in stem cell maintenance and somatic cell reprogramming.
多能性的获得在很大程度上是由激活因子OCT4、SOX2和NANOG在转录水平上驱动的,而这些激活因子反过来又必须与多种共激活因子合作,以执行干细胞特异性基因表达程序。利用一种生化定义的体外转录系统,该系统介导OCT4/SOX2以及基因的共激活因子依赖性转录,我们报告了对戴斯科林(DKC1)核糖核蛋白复合体的纯化和鉴定,它是一种OCT4/SOX2共激活因子,其活性似乎受相关小核仁RNA(snoRNA)的一个子集调节。DKC1复合体占据增强子并调节对胚胎干细胞(ES细胞)自我更新至关重要的关键多能性基因的表达。成纤维细胞中DKC1的缺失显著降低了诱导多能干细胞(iPS细胞)的生成效率。因此,这项研究揭示了DKC1复合体在干细胞维持和体细胞重编程中意想不到的转录作用。