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体内糖皮质激素受体介导的染色质重塑

Glucocorticoid receptor-mediated chromatin remodeling in vivo.

作者信息

Deroo B J, Archer T K

机构信息

Chromatin and Gene Expression Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina, NC 27709, USA.

出版信息

Oncogene. 2001 May 28;20(24):3039-46. doi: 10.1038/sj.onc.1204328.

Abstract

The compaction of DNA into chromatin provides an additional level of gene regulation in eukaryotes that may not be available to prokaryotes. When packaged as chromatin, most promoters are transcriptionally repressed, and transcription factors have reduced access to their binding sites. The glucocorticoid receptor (GR) is a ligand-activated transcription factor that regulates the activity of genes involved in many physiological processes. To regulate eukaryotic genes, the GR binds to target sites within promoter regions of genes assembled as chromatin. This interaction alters the nucleosomal architecture to allow binding of other transcription factors, and formation of the preinitiation complex. The mouse mammary tumor virus (MMTV) promoter has been used extensively as a model to explore the processes by which the GR remodels chromatin and activates transcription. Significant progress has been made in our understanding of the mechanisms used by the GR to modify chromatin structure, and the limits placed on the GR by post-translational modifications of histones. We will describe recent developments in the processes used by the GR to activate transcription in vivo via chromatin remodeling complexes, histone H1 phosphorylation, and recruitment of diverse coactivators.

摘要

DNA压缩成染色质为真核生物提供了额外的基因调控水平,而原核生物可能没有这种调控方式。当包装成染色质时,大多数启动子会受到转录抑制,转录因子与它们的结合位点的接触也会减少。糖皮质激素受体(GR)是一种配体激活的转录因子,可调节参与许多生理过程的基因的活性。为了调控真核基因,GR会与组装成染色质的基因启动子区域内的靶位点结合。这种相互作用会改变核小体结构,以允许其他转录因子结合并形成预起始复合物。小鼠乳腺肿瘤病毒(MMTV)启动子已被广泛用作模型,以探索GR重塑染色质并激活转录的过程。我们在理解GR用于修饰染色质结构的机制以及组蛋白翻译后修饰对GR的限制方面取得了重大进展。我们将描述GR通过染色质重塑复合物、组蛋白H1磷酸化以及募集各种共激活因子在体内激活转录过程中的最新进展。

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