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酵母HAP1激活剂与因子RC2竞争结合CYC1基因的上游激活位点UAS1。

Yeast HAP1 activator competes with the factor RC2 for binding to the upstream activation site UAS1 of the CYC1 gene.

作者信息

Pfeifer K, Arcangioli B, Guarente L

出版信息

Cell. 1987 Apr 10;49(1):9-18. doi: 10.1016/0092-8674(87)90750-1.

Abstract

We show that the yeast HAP1 activator locus encodes a protein that binds in vitro to the upstream activation site, UAS1, of the CYC1 gene (iso-1-cytochrome c). Binding of wild-type HAP1 and truncated HAP1 derivatives to UAS1 is evident in crudely fractionated yeast extracts using the gel electrophoresis DNA binding assay. The binding of HAP1 in vitro, like the activity of UAS1 in vivo, is stimulated by heme. HAP1 binds to region B, one of two portions of UAS1 shown to be important by genetic analysis of the site. Surprisingly, HAP1 binds to the same sequence as a second factor, RC2. Both HAP1 and RC2 bind to the same side of the helix, and make similar but not identical major and minor groove contacts that span two full turns. An additional factor that binds to the second important part of UAS1, the region A factor (RAF), is also identified. A model depicting the interplay of HAP1, RC2, and RAF in the control of UAS1 is presented.

摘要

我们发现酵母HAP1激活基因座编码一种蛋白质,该蛋白质在体外可与CYC1基因(同工酶1 - 细胞色素c)的上游激活位点UAS1结合。使用凝胶电泳DNA结合试验,在粗分级的酵母提取物中可明显观察到野生型HAP1和截短的HAP1衍生物与UAS1的结合。HAP1在体外的结合,如同UAS1在体内的活性一样,受到血红素的刺激。HAP1与区域B结合,区域B是通过对该位点的遗传分析显示为重要的UAS1的两个部分之一。令人惊讶的是,HAP1与第二个因子RC2结合相同的序列。HAP1和RC2都结合在螺旋的同一侧,并形成跨越两个完整螺旋圈的相似但不完全相同的大沟和小沟接触。还鉴定出另一个与UAS1的第二个重要部分结合的因子,即区域A因子(RAF)。本文提出了一个描述HAP1、RC2和RAF在UAS1控制中的相互作用的模型。

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