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小鼠糖皮质激素受体:通过野生型和突变型受体蛋白的克隆、测序及表达对功能结构域进行定位

The mouse glucocorticoid receptor: mapping of functional domains by cloning, sequencing and expression of wild-type and mutant receptor proteins.

作者信息

Danielsen M, Northrop J P, Ringold G M

出版信息

EMBO J. 1986 Oct;5(10):2513-22. doi: 10.1002/j.1460-2075.1986.tb04529.x.

Abstract

We have isolated mouse glucocorticoid receptor (GR) cDNAs which, when expressed in transfected mammalian cells, produce a fully functional GR protein. Sequence analysis reveals an open reading frame of 2349 bp which could encode a protein of approximately 86,000 daltons. We have also isolated two receptor cDNAs from mouse S49 nuclear transfer-deficient (nt-) cells which encode mutant forms of the receptor protein. One cDNA encodes a protein that is unable to bind hormone and represents the endogenous hormone binding deficient receptor recently discovered in S49 cells. The lesion in this receptor is due to a single amino acid substitution (Glu-546 to Gly). The second cDNA from nt- cells produces a receptor protein that is able to bind hormone but has reduced nuclear binding. This cDNA, therefore, encodes for the S49 nt- receptor which has been shown to have reduced affinity for DNA. The lesion maps to a single amino acid substitution (Arg-484 to His) located in a highly Cys, Lys, Arg-rich region of the protein previously implicated in DNA binding. Our studies provide unambiguous identification of receptor domains and specific amino acids critical for the hormone and DNA binding properties of this transcriptional regulatory protein. Contained within the first 106 amino acids of the mouse GR is a stretch of nine glutamines with two prolines which are related to the family of transcribed repetitive elements, opa, found in Drosophila melanogaster. A truncated receptor lacking these 106 amino acids is functionally indistinguishable from the wild-type receptor.

摘要

我们已经分离出小鼠糖皮质激素受体(GR)的cDNA,当它们在转染的哺乳动物细胞中表达时,会产生一种功能完全正常的GR蛋白。序列分析显示有一个2349 bp的开放阅读框,它可能编码一种约86,000道尔顿的蛋白质。我们还从小鼠S49核转运缺陷(nt-)细胞中分离出了两种受体cDNA,它们编码受体蛋白的突变形式。一种cDNA编码的蛋白质无法结合激素,代表了最近在S49细胞中发现的内源性激素结合缺陷型受体。这种受体的损伤是由于单个氨基酸替换(Glu-546突变为Gly)。来自nt-细胞的第二个cDNA产生一种能够结合激素但核结合能力降低的受体蛋白。因此,这个cDNA编码S49 nt-受体,已证明它对DNA的亲和力降低。损伤定位到位于该蛋白质富含半胱氨酸、赖氨酸、精氨酸的区域中的单个氨基酸替换(Arg-484突变为His),该区域先前与DNA结合有关。我们的研究明确鉴定了该转录调节蛋白的受体结构域以及对其激素和DNA结合特性至关重要的特定氨基酸。在小鼠GR的前106个氨基酸中包含一段由九个谷氨酰胺和两个脯氨酸组成的序列,这与在果蝇中发现的转录重复元件opa家族有关。缺少这106个氨基酸的截短型受体在功能上与野生型受体没有区别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c9/1167147/e8b01118ea20/emboj00173-0108-a.jpg

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