Reiter Franziska, Wienerroither Sebastian, Stark Alexander
Research Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus-Vienna-Biocenter 1, 1030 Vienna, Austria.
Research Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus-Vienna-Biocenter 1, 1030 Vienna, Austria.
Curr Opin Genet Dev. 2017 Apr;43:73-81. doi: 10.1016/j.gde.2016.12.007. Epub 2017 Jan 19.
Differential gene expression gives rise to the many cell types of complex organisms. Enhancers regulate transcription by binding transcription factors (TFs), which in turn recruit cofactors to activate RNA Polymerase II at core promoters. Transcriptional regulation is typically mediated by distinct combinations of TFs, enabling a relatively small number of TFs to generate a large diversity of cell types. However, how TFs achieve combinatorial enhancer control and how enhancers, enhancer-bound TFs, and the cofactors they recruit regulate RNA Polymerase II activity is not entirely clear. Here, we review how TF synergy is mediated at the level of DNA binding and after binding, the role of cofactors and the post-translational modifications they catalyze, and discuss different models of enhancer-core-promoter communication.
差异基因表达产生了复杂生物体的多种细胞类型。增强子通过结合转录因子(TFs)来调节转录,转录因子进而招募辅因子以在核心启动子处激活RNA聚合酶II。转录调控通常由不同组合的转录因子介导,使得相对少量的转录因子能够产生多种多样的细胞类型。然而,转录因子如何实现组合式增强子控制,以及增强子、与增强子结合的转录因子及其招募的辅因子如何调节RNA聚合酶II的活性,目前尚不完全清楚。在此,我们综述转录因子协同作用在DNA结合水平以及结合后是如何介导的、辅因子的作用及其催化的翻译后修饰,并讨论增强子 - 核心启动子通讯的不同模型。