O'Donnell Amanda, Yang Shen-Hsi, Sharrocks Andrew D
Faculty of Life Sciences, University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Mol Cell. 2008 Mar 28;29(6):780-5. doi: 10.1016/j.molcel.2008.01.019.
Gene activation is often associated with high levels of histone acetylation. Enhanced acetylation levels can promote the recruitment of further chromatin modifying complexes or the basal transcription machinery. Here, we have studied MAP kinase-mediated upregulation of c-fos and uncover a role for histone acetylation in promoting the recruitment of a second transcription factor, NFI. MAP kinase signaling to Elk-1 enhances the net histone acetylase activity associated with the c-fos promoter, which leads to changes in the acetylation state and structure of a promoter-proximal nucleosome, which allows NFI binding. Binding of NFI provides a permissive state for the recruitment of basal machinery and subsequent promoter activation. Our results provide insights into how MAP kinase signaling promotes inducible gene expression; phosphorylation of recipient transcription factors (primary effectors) triggers a HAT relay switch, which facilitates the recruitment of additional transcription factors (secondary effectors) through alteration of the local nucleosomal structure.
基因激活通常与高水平的组蛋白乙酰化相关。增强的乙酰化水平可促进进一步的染色质修饰复合物或基础转录机制的募集。在此,我们研究了丝裂原活化蛋白激酶(MAP激酶)介导的c-fos上调,并揭示了组蛋白乙酰化在促进第二种转录因子NFI募集方面的作用。MAP激酶向Elk-1的信号传导增强了与c-fos启动子相关的净组蛋白乙酰转移酶活性,这导致启动子近端核小体的乙酰化状态和结构发生变化,从而允许NFI结合。NFI的结合为基础机制的募集和随后的启动子激活提供了许可状态。我们的结果为MAP激酶信号传导如何促进诱导型基因表达提供了见解;受体转录因子(主要效应物)的磷酸化触发了组蛋白乙酰转移酶(HAT)中继开关,通过改变局部核小体结构促进了额外转录因子(次要效应物)的募集。