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生理上不相关的转录因子通过协同DNA结合实现转录的协同激活。

Synergistic activation of transcription by physiologically unrelated transcription factors through cooperative DNA-binding.

作者信息

Vashee S, Willie J, Kodadek T

机构信息

Department of Chemistry and Biochemistry and the Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, 78712-1096, USA.

出版信息

Biochem Biophys Res Commun. 1998 Jun 18;247(2):530-5. doi: 10.1006/bbrc.1998.8820.

Abstract

Most eukaryotic promoters contain binding sites for several different transcription factors, which often act synergistically. Mechanistically, synergy is ascribed either to cooperative DNA-binding of the factors to the promoter or to some type of "multiple contact" mechanism in which each activator performs a different task in stimulating the transcription machinery. Here, it is shown that the yeast activators Gal4 and Put3 bind to DNA cooperatively in vivo and can activate transcription synergistically from certain synthetic promoters. Normally, Gal4 and Put3 bind to completely different promoters and activate physiologically unrelated sets of genes and it is extremely unlikely that they have evolved direct protein-protein contacts. These studies add to a growing body of evidence that binding of proteins to nearby sites in chromatin is intrinsically cooperative and suggest that many examples of synergy ascribed to multiple contact mechanisms may instead involve non-traditional cooperative DNA-binding.

摘要

大多数真核生物启动子包含几个不同转录因子的结合位点,这些转录因子通常协同发挥作用。从机制上讲,协同作用要么归因于这些因子与启动子的协同DNA结合,要么归因于某种类型的“多重接触”机制,其中每个激活剂在刺激转录机制时执行不同的任务。在此,研究表明酵母激活剂Gal4和Put3在体内协同结合DNA,并能从某些合成启动子协同激活转录。正常情况下,Gal4和Put3结合到完全不同的启动子上,并激活生理上不相关的基因集,而且它们极不可能进化出直接的蛋白质-蛋白质接触。这些研究增加了越来越多的证据,即蛋白质与染色质中附近位点的结合本质上是协同的,并表明许多归因于多重接触机制的协同作用例子可能反而涉及非传统的协同DNA结合。

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