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新型真核转录抑制因子。

New eukaryotic transcriptional repressors.

作者信息

Saha S, Brickman J M, Lehming N, Ptashne M

机构信息

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Nature. 1993 Jun 17;363(6430):648-52. doi: 10.1038/363648a0.

Abstract

Transcriptional activating sequences have been described that are encoded by parts of the genome of Escherichia coli. These acidic peptides, fused to a DNA-binding fragment of the yeast transcriptional activator GAL4, activate transcription of a gene in a wide array of eukaryotes, provided that gene bears GAL4-binding sites nearby. Here we describe an E. coli-encoded sequence that, when attached to the same DNA-binding fragment (GAL4(1-147)), converts that fragment into a repressor. Thus, as assayed in yeast or in vitro in yeast extracts, this molecule represses transcription when bound upstream of a variety of different activators. Two additional repressing regions that work when tethered upstream, a multiple mutant derivative of the original isolate and a synthetic peptide are, like the original isolate, highly basic. At least one activator can be inhibited by the mutant but not by the parental repressing region. These and other findings suggest that these repressing regions interact with and inhibit the activity of activating regions bound nearby on DNA.

摘要

已经描述了由大肠杆菌基因组的部分编码的转录激活序列。这些酸性肽与酵母转录激活因子GAL4的DNA结合片段融合,只要该基因在附近带有GAL4结合位点,就能在多种真核生物中激活基因转录。在此,我们描述了一种大肠杆菌编码的序列,当它连接到相同的DNA结合片段(GAL4(1 - 147))时,会将该片段转化为一种阻遏物。因此,正如在酵母中或在酵母提取物的体外实验中所检测到的,当该分子结合在多种不同激活因子的上游时,会抑制转录。另外两个在上游拴系时起作用的阻遏区域、原始分离株的一个多突变衍生物以及一个合成肽,与原始分离株一样,具有高度碱性。至少有一种激活因子可被该突变体抑制,但不能被亲本阻遏区域抑制。这些以及其他发现表明,这些阻遏区域与结合在DNA上附近的激活区域相互作用并抑制其活性。

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