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类固醇激素的转录调控

Transcriptional regulation by steroid hormones.

作者信息

Beato M, Chávez S, Truss M

机构信息

Institut für Molekularbiologie und Tumorforschung, Marburg, Germany.

出版信息

Steroids. 1996 Apr;61(4):240-51. doi: 10.1016/0039-128x(96)00030-x.

Abstract

Steroid hormones influence the transcription of a large number of genes by virtue of their interaction with intracellular receptors, which are modular proteins composed of a ligand binding domain, a DNA binding domain, and several transactivation functions distributed along the molecule. The DNA binding domain is organized around two zinc ions and allows the receptors to bind as homodimers to palindromic DNA sequences, the hormones responsive elements (HRE), is such a way that each homodimer contacts one half of the palindrome. Since the two halves are separated by three base pairs, the two homodimers contact the same face of the double helix. Before hormone binding, the receptors are part of a complex with multiple chaperones which maintain the receptor in its steroid binding conformation. Following hormone binding, the complex dissociates and the receptors bind to HREs in chromatin. Regulation of gene expression by hormones involves an interaction of the DNA-bound receptors with other sequence-specific transcription factors and with the general transcription factors, which is partly mediated by co-activators and co-repressors. The specific array of cis regulatory elements in a particular promoter/enhancer region, as well as the organization of the DNA sequences in nucleosomes, specifies the network of receptor interactions. Depending on the nature of these interactions, the final outcome can be induction or repression of transcription. The various levels at which these interactions are modulated are discussed using as an example the promoter of the Mouse Mammary Tumor Virus and its organization in chromatin.

摘要

类固醇激素通过与细胞内受体相互作用来影响大量基因的转录,这些受体是由配体结合域、DNA结合域以及沿分子分布的几种反式激活功能组成的模块化蛋白质。DNA结合域围绕两个锌离子组织,使受体以同二聚体形式结合到回文DNA序列(激素反应元件,HRE)上,使得每个同二聚体与回文的一半接触。由于两半由三个碱基对隔开,两个同二聚体接触双螺旋的同一面。在激素结合之前,受体是与多种伴侣蛋白形成的复合物的一部分,这些伴侣蛋白将受体维持在其类固醇结合构象中。激素结合后,复合物解离,受体与染色质中的HRE结合。激素对基因表达的调控涉及与DNA结合的受体与其他序列特异性转录因子以及通用转录因子的相互作用,这部分是由共激活因子和共抑制因子介导的。特定启动子/增强子区域中顺式调控元件的特定排列以及核小体中DNA序列的组织,决定了受体相互作用的网络。根据这些相互作用的性质,最终结果可能是转录的诱导或抑制。以小鼠乳腺肿瘤病毒的启动子及其在染色质中的组织为例,讨论了这些相互作用被调节的各个水平。

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