Vicent Guillermo P, Nacht A Silvina, Zaurín Roser, Ballaré Cecilia, Clausell Jaime, Beato Miguel
Centre de Regulació Genòmica, Universitat Pompeu Fabra, Parc de Recerca Biomèdica, Aiguader 88, E-08003 Barcelona, Spain.
Mol Endocrinol. 2010 Nov;24(11):2088-98. doi: 10.1210/me.2010-0027. Epub 2010 May 19.
Steroid hormones regulate gene expression by interaction of their receptors with hormone-responsive elements on DNA or with other transcription factors, but they can also activate cytoplasmic signaling cascades. Rapid activation of Erk by progestins via an interaction of the progesterone receptor (PR) with the estrogen receptor is critical for transcriptional activation of the mouse mammary tumor virus (MMTV) promoter and other progesterone target genes. Erk activation leads to the phosphorylation of PR, activation of mitogen- and stress-activated protein kinase 1, and the recruitment of a complex of the three activated proteins and of P300/CBP-associated factor (PCAF) to a single nucleosome, resulting in the phosphoacetylation of histone H3 and the displacement of heterochromatin protein 1γ. Hormone-dependent gene expression requires ATP-dependent chromatin remodeling complexes. Two switch/sucrose nonfermentable-like complexes, Brahma-related gene 1-associated factor (BAF) and polybromo-BAF are present in breast cancer cells, but only BAF is recruited to the MMTV promoter and cooperates with PCAF during activation of hormone-responsive promoters. PCAF acetylates histone H3 at K14, an epigenetic mark recognized by BAF subunits, thus anchoring the complex to chromatin. BAF catalyzes localized displacement of histones H2A and H2B, facilitating access of nuclear factor 1 and additional PR complexes to the hidden hormone-responsive elements on the MMTV promoter. The linker histone H1 is a structural component of chromatin generally regarded as a general repressor of transcription. However, it contributes to a better regulation of the MMTV promoter by favoring a more homogeneous nucleosome positioning, thus reducing basal transcription and actually enhancing hormone induced transcription. During transcriptional activation, H1 is phosphorylated and displaced from the promoter. The kinase cyclin-dependent kinase 2 is activated after progesterone treatment and could catalyze progesterone-induced phosphorylation of histone H1 by chromatin remodeling complexes. The initial steps of gene induction by progestins involve changes in the chromatin organization of target promoters that require the activation of several kinase signaling pathways initiated by membrane anchored PR. Because these pathways also respond to other external signals, they serve to integrate the hormonal response in the global context of the cellular environment.
类固醇激素通过其受体与DNA上的激素反应元件或其他转录因子相互作用来调节基因表达,但它们也能激活细胞质信号级联反应。孕激素通过孕酮受体(PR)与雌激素受体相互作用快速激活Erk,这对小鼠乳腺肿瘤病毒(MMTV)启动子和其他孕酮靶基因的转录激活至关重要。Erk激活导致PR磷酸化、丝裂原和应激激活蛋白激酶1激活,以及三种激活蛋白和P300/CBP相关因子(PCAF)的复合物募集到单个核小体,导致组蛋白H3磷酸乙酰化和异染色质蛋白1γ位移。激素依赖性基因表达需要ATP依赖性染色质重塑复合物。乳腺癌细胞中存在两种类似开关/蔗糖非发酵复合物,即与婆罗门相关基因1相关因子(BAF)和多溴BAF,但只有BAF被募集到MMTV启动子,并在激素反应性启动子激活过程中与PCAF协同作用。PCAF在K14位点乙酰化组蛋白H3,这是一个被BAF亚基识别的表观遗传标记,从而将复合物锚定到染色质上。BAF催化组蛋白H2A和H2B的局部位移,促进核因子1和其他PR复合物进入MMTV启动子上隐藏的激素反应元件。连接组蛋白H1是染色质的结构成分,通常被视为转录的一般抑制因子。然而,它通过促进更均匀的核小体定位来更好地调节MMTV启动子,从而减少基础转录并实际上增强激素诱导的转录。在转录激活过程中,H1被磷酸化并从启动子上位移。孕酮处理后,细胞周期蛋白依赖性激酶2被激活,并可催化染色质重塑复合物对组蛋白H1进行孕酮诱导的磷酸化。孕激素诱导基因的初始步骤涉及靶启动子染色质组织的变化,这需要激活由膜锚定PR启动的几种激酶信号通路。由于这些通路也对其他外部信号作出反应,它们有助于在细胞环境的整体背景下整合激素反应。