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甲状腺激素受体的第二个锌指突变体选择性地保留DNA结合和异源二聚化能力,但消除转录激活作用。

Second zinc finger mutants of thyroid hormone receptor selectively preserve DNA binding and heterodimerization but eliminate transcriptional activation.

作者信息

Nagaya T, Kopp P, Kitajima K, Jameson J L, Seo H

机构信息

Department of Endocrinology and Metabolism, Nagoya University, Japan.

出版信息

Biochem Biophys Res Commun. 1996 May 15;222(2):524-30. doi: 10.1006/bbrc.1996.0777.

Abstract

Transcriptional regulation by thyroid hormone is mediated through its nuclear receptors (TRs), which bind to target responsive elements as homodimers or as heterodimers with 9-cis retinoic acid receptors (RXRs). We examined the dimerization and functional properties of TRs containing mutations in the first and second zinc finger regions of the DNA binding domain. Interestingly, a mutation (R158G) in the loop of second zinc finger, or a chimeric mutant in which the second zinc finger of the glucocorticoid receptor (GR) was substituted for that of the TR, did not form homodimer, but still bound as a heterodimer with RXR alpha. Despite the presence of heterodimer formation, these mutants were functionally inactive in transfection assays. We conclude that sequences within the loop of the second zinc finger may play an important role in stability in vivo or transcriptional activation of the TR.

摘要

甲状腺激素的转录调控是通过其核受体(TRs)介导的,TRs作为同二聚体或与9-顺式视黄酸受体(RXRs)形成异二聚体与靶反应元件结合。我们研究了在DNA结合域的第一和第二个锌指区域含有突变的TRs的二聚化和功能特性。有趣的是,第二个锌指环中的一个突变(R158G),或者一个嵌合突变体,其中糖皮质激素受体(GR)的第二个锌指替代了TR的第二个锌指,不形成同二聚体,但仍作为与RXRα的异二聚体结合。尽管存在异二聚体形成,但这些突变体在转染实验中功能无活性。我们得出结论,第二个锌指环内的序列可能在TR在体内的稳定性或转录激活中起重要作用。

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