Wang Zheng-Xu, Teh Christina Hui-Leng, Kueh Jacqueline L L, Lufkin Thomas, Robson Paul, Stanton Lawrence W
Department of Stem Cell and Developmental Biology, Genome Institute of Singapore, Singapore 138672.
J Biol Chem. 2007 Apr 27;282(17):12822-30. doi: 10.1074/jbc.M611814200. Epub 2007 Mar 7.
It is well known that Oct4 and Sox2 play an important role in the maintenance of embryonic stem cell pluripotency. These transcription factors bind to regulatory regions within hundreds of target genes to control their expression. Zfp206 is a recently characterized transcription factor that has a role in maintaining stem cell pluripotency. We have demonstrated here that Zfp206 is a direct downstream target of Oct4 and Sox2. Two composite sox-oct binding sites have been identified within the first intron of Zfp206. We have demonstrated binding of Oct4 and Sox2 to this region. In addition, we have shown that Oct4 or Sox2 alone can activate transcription via one of these sox-oct elements, although the presence of both Oct4 and Sox2 gave rise to a synergistic effect. These studies extend our understanding of the transcriptional network that operates to regulate the differentiation potential of embryonic stem cells.
众所周知,Oct4和Sox2在维持胚胎干细胞多能性方面发挥着重要作用。这些转录因子与数百个靶基因内的调控区域结合以控制它们的表达。Zfp206是最近鉴定出的一种在维持干细胞多能性中起作用的转录因子。我们在此证明Zfp206是Oct4和Sox2的直接下游靶标。在Zfp206的第一个内含子内已鉴定出两个复合的sox-oct结合位点。我们已证明Oct4和Sox2与该区域结合。此外,我们已表明单独的Oct4或Sox2可通过这些sox-oct元件之一激活转录,尽管Oct4和Sox2同时存在会产生协同效应。这些研究扩展了我们对调控胚胎干细胞分化潜能的转录网络的理解。