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皮质类固醇作用的分子遗传学

Molecular genetics of corticosteroid action.

作者信息

Miesfeld R L

机构信息

Department of Biochemistry, University of Arizona Cancer Center, Tucson.

出版信息

Am Rev Respir Dis. 1990 Feb;141(2 Pt 2):S11-7.

PMID:2178510
Abstract

The recent isolation and characterization of steroid receptor coding sequences has revolutionized the field of steroid hormone action. These studies have revealed that steroid receptors are members of a much larger nuclear receptor "super family." The ligand and DNA binding domains have been shown to be molecular components that functionally interact to transform the steroid-receptor complex into a highly specific gene regulator that induces or represses the expression of cell-specific target genes. Molecular genetic approaches have been used to study structure-function relationships of several steroid receptor proteins, the most extensive analysis has been that of the glucocorticoid receptor. Several breakthroughs in the study of steroid hormone action include the construction of novel chimeric steroid receptor proteins, functional expression of steroid receptors in yeast, and the development of sensitive cloning techniques designed to isolate low abundance, hormonally regulated transcripts.

摘要

近期对类固醇受体编码序列的分离和特性鉴定彻底改变了类固醇激素作用领域。这些研究表明,类固醇受体是一个大得多的核受体“超家族”的成员。配体和DNA结合结构域已被证明是功能性相互作用的分子成分,可将类固醇-受体复合物转化为高度特异性的基因调节因子,诱导或抑制细胞特异性靶基因的表达。分子遗传学方法已被用于研究几种类固醇受体蛋白的结构-功能关系,其中对糖皮质激素受体的分析最为广泛。类固醇激素作用研究中的几个突破包括构建新型嵌合类固醇受体蛋白、在酵母中功能性表达类固醇受体,以及开发旨在分离低丰度、激素调节转录本的灵敏克隆技术。

相似文献

1
Molecular genetics of corticosteroid action.皮质类固醇作用的分子遗传学
Am Rev Respir Dis. 1990 Feb;141(2 Pt 2):S11-7.
2
A novel, highly conserved structural motif is present in all members of the steroid receptor superfamily.一种新颖的、高度保守的结构基序存在于类固醇受体超家族的所有成员中。
Receptor. 1992 Winter;2(4):225-40.
3
Glucocorticoid receptor mutants that are constitutive activators of transcriptional enhancement.作为转录增强组成型激活剂的糖皮质激素受体突变体。
Nature. 1987;325(6102):365-8. doi: 10.1038/325365a0.
4
Analysis of the hormone-binding domain of steroid receptors using chimeras generated by homologous recombination.利用同源重组产生的嵌合体分析类固醇受体的激素结合结构域。
Exp Cell Res. 2005 Aug 15;308(2):320-33. doi: 10.1016/j.yexcr.2005.03.040.
5
Oestrogen and glucocorticoid responsive elements are closely related but distinct.雌激素反应元件和糖皮质激素反应元件密切相关但又有所不同。
Nature. 1987;329(6141):734-6. doi: 10.1038/329734a0.
6
Structure-function aspects of the glucocorticoid receptor.
Princess Takamatsu Symp. 1990;21:137-55.
7
Glucocorticoid receptor beta, a potential endogenous inhibitor of glucocorticoid action in humans.糖皮质激素受体β,一种人类糖皮质激素作用的潜在内源性抑制剂。
J Clin Invest. 1995 Jun;95(6):2435-41. doi: 10.1172/JCI117943.
8
Human steroid receptors and erb-A gene products form a superfamily of enhancer-binding proteins.人类类固醇受体和erb - A基因产物构成了一个增强子结合蛋白超家族。
Clin Physiol Biochem. 1987;5(3-4):179-89.
9
Genetic dissection of corticosteroid receptor function in mice.小鼠中皮质类固醇受体功能的遗传学剖析
Horm Metab Res. 2004 Jun;36(6):387-91. doi: 10.1055/s-2004-814567.
10
Oestradiol induction of a glucocorticoid-responsive gene by a chimaeric receptor.嵌合受体介导的雌二醇对糖皮质激素反应性基因的诱导作用。
Nature. 1987;325(6099):75-8. doi: 10.1038/325075a0.

引用本文的文献

1
Repression of transcription by the glucocorticoid receptor: A parsimonious model for the genomics era.糖皮质激素受体对转录的抑制:基因组时代的简约模型。
J Biol Chem. 2021 Jan-Jun;296:100687. doi: 10.1016/j.jbc.2021.100687. Epub 2021 Apr 21.
2
An overview of glucocorticoid anti-inflammatory actions.糖皮质激素抗炎作用概述。
Eur J Clin Pharmacol. 1993;45 Suppl 1:S3-7; discussion S43-4. doi: 10.1007/BF01844196.
3
nti glucocorticoid receptor transcripts lack sequences encoding the amino-terminal transcriptional modulatory domain.
抗糖皮质激素受体转录本缺乏编码氨基末端转录调节结构域的序列。
Mol Cell Biol. 1990 Sep;10(9):4574-81. doi: 10.1128/mcb.10.9.4574-4581.1990.
4
Transcriptional transactivation functions localized to the glucocorticoid receptor N terminus are necessary for steroid induction of lymphocyte apoptosis.定位于糖皮质激素受体N端的转录反式激活功能对于类固醇诱导淋巴细胞凋亡是必需的。
Mol Cell Biol. 1992 Feb;12(2):589-97. doi: 10.1128/mcb.12.2.589-597.1992.