Suppr超能文献

通过克隆受体cDNA的表达对糖皮质激素受体缺陷进行基因互补。

Genetic complementation of a glucocorticoid receptor deficiency by expression of cloned receptor cDNA.

作者信息

Miesfeld R, Rusconi S, Godowski P J, Maler B A, Okret S, Wikström A C, Gustafsson J A, Yamamoto K R

出版信息

Cell. 1986 Aug 1;46(3):389-99. doi: 10.1016/0092-8674(86)90659-8.

Abstract

We isolated and sequenced 6.3 kb of cDNA encoding that rat glucocorticoid receptor, a protein that binds and activates a class of hormone-dependent transcriptional enhancers. Receptor-containing cells produce receptor mRNAs of approximately equal to 6.5 kb and approximately equal to 4.8 kb that differ only in their 3' nontranslated regions; an open reading frame of 795 amino acids resides within the 5' portion of the transcripts. The coding region was expressed in vitro, in transient transfections, and in stable transfectants of a receptor-deficient cell line. The protein products are indistinguishable from bona fide receptor with respect to sedimentation and electrophoretic mobility, antibody reactivity, and hormone and DNA binding. Moreover, the cloned receptor protein activates its corresponding enhancers, restoring to the receptor-deficient cells the full capacity for regulated enhancement.

摘要

我们分离并测序了编码大鼠糖皮质激素受体的6.3 kb互补DNA,该受体是一种能结合并激活一类激素依赖性转录增强子的蛋白质。含受体的细胞产生大小约为6.5 kb和4.8 kb的受体信使核糖核酸,二者仅在3'非翻译区有所不同;795个氨基酸的开放阅读框位于转录本的5'部分。编码区在体外、瞬时转染以及受体缺陷细胞系的稳定转染子中均有表达。蛋白质产物在沉降、电泳迁移率、抗体反应性以及激素和DNA结合方面与真正的受体无法区分。此外,克隆的受体蛋白激活其相应的增强子,使受体缺陷细胞恢复完全的调节增强能力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验