Nuclear receptor corepressors.

Nuclear receptor signaling Pub Date : 2003-01-01 Epub Date: 2003-06-12 DOI:10.1621/nrs.01001
Mitchell A Lazar
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引用次数: 59

Abstract

The ability of NR LBDs to transfer repression function to a heterologous DNA binding domain, and the cross-squelching of repression by untethered LBDs, has suggested that repression is mediated by interactions with putative cellular corepressor proteins. The yeast-two hybrid screen for protein interactors has proven to be the key to the isolation and characterization of corepressors. This short review will focus on N-CoR and SMRT.

核受体辅抑制因子。
NR lbd将抑制功能转移到异源DNA结合域的能力,以及非系带lbd对抑制的交叉抑制,表明抑制是通过与假定的细胞协同抑制蛋白相互作用介导的。酵母- 2杂交筛选蛋白相互作用物已被证明是分离和表征辅抑制物的关键。这篇简短的综述将集中在N-CoR和SMRT上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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