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配体结合域中的特定突变选择性地消除了人类甲状腺激素受体β的沉默功能。

Specific mutations in the ligand binding domain selectively abolish the silencing function of human thyroid hormone receptor beta.

作者信息

Nawaz Z, Tsai M J, O'Malley B W

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Dec 5;92(25):11691-5. doi: 10.1073/pnas.92.25.11691.

Abstract

Although most nuclear hormone receptors are ligand-dependent transcriptional activators, certain members of this superfamily, such as thyroid hormone receptor (TR) and retinoic acid receptor (RAR), are involved in transcriptional repression. The silencing function of these receptors has been localized to the ligand binding domain (LBD). Previously, we demonstrated that overexpression of either the entire LBD or only the N-terminal region of the LBD (amino acids 168-259) is able to inhibit the silencing activity of TR. From this result we postulated the existence of a limiting factor (corepressor) that is necessary for TR silencing activity. To support this hypothesis, we identified amino acids in the N-terminal region of the LBD of TR that are important for the corepressor interaction and for the silencing function of TR. The silencing activity of TR was unaffected by overexpression of the LBD of mutant TR (V174A/D177A), suggesting that valine at position 174 and/or aspartic acid at position 177 are important for corepressor interaction. This mutant receptor protein, V174/D177, also lost the ability to silence target genes, suggesting that these amino acids are important for silencing function. Control experiments indicate that this mutant TR maintains its wild-type hormone binding and transactivation functions. These findings further strengthen the idea that the N-terminal region of the LBD of TR interacts with a putative corepressor protein(s) to achieve silencing of basal gene transcription.

摘要

虽然大多数核激素受体是配体依赖性转录激活因子,但该超家族的某些成员,如甲状腺激素受体(TR)和视黄酸受体(RAR),却参与转录抑制。这些受体的沉默功能已定位到配体结合域(LBD)。此前,我们证明,全长LBD或仅LBD的N端区域(氨基酸168 - 259)的过表达能够抑制TR的沉默活性。基于这一结果,我们推测存在一种对TR沉默活性必不可少的限制因子(共抑制因子)。为支持这一假说,我们确定了TR的LBD N端区域中对共抑制因子相互作用和TR沉默功能至关重要的氨基酸。突变型TR(V174A/D177A)的LBD过表达对TR的沉默活性没有影响,这表明174位的缬氨酸和/或177位的天冬氨酸对共抑制因子相互作用很重要。这种突变受体蛋白V174/D177也失去了沉默靶基因的能力,这表明这些氨基酸对沉默功能很重要。对照实验表明,这种突变型TR保持其野生型激素结合和反式激活功能。这些发现进一步强化了这样一种观点,即TR的LBD N端区域与一种假定的共抑制因子蛋白相互作用,以实现基础基因转录的沉默。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cda9/40468/7e6e30f96c6d/pnas01503-0380-a.jpg

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