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驱动酵母TBP编码基因SPT15转录的显性正调控元件的生化与遗传学特征分析

Biochemical and genetic characterization of the dominant positive element driving transcription ofthe yeast TBP-encoding gene, SPT15.

作者信息

Schroeder S C, Weil P A

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville,TN 37232-0615, USA.

出版信息

Nucleic Acids Res. 1998 Sep 15;26(18):4186-95. doi: 10.1093/nar/26.18.4186.

Abstract

We previously demonstrated that a combination of both positive and negative cis -acting upstream elements control the transcription of the gene encoding TBP ( SPT15 ) in Saccharomyces cerevisiae . One of these elements found in that study, resident between 5' flanking sequences -147 and -128 , and termed PED (for positive element distal), was found to play an essential positive role in driving transcription of the gene encoding TBP. In this report, we map at nucleotide-level resolution, the critical residues which comprise PED, purify and sequence the protein that binds to it and determine that this PED binding factor is Abf1p, an abundant yeast protein previously broadly implicated in both gene regulation and DNA replication. In the case of the TBP-encoding gene, however, Abf1p works through the PED element which is a non-consensus binding site. Based upon the work of others, the PED-variant ABF1 site would be predicted to be a very poor binding site for this factor yet Abf1p binds PED and a consensus ABF1 site with comparable affinity. These results are discussed in light of the broader context of Abf1p-mediated gene regulation.

摘要

我们先前证明,正向和负向顺式作用上游元件的组合控制酿酒酵母中编码TBP(SPT15)的基因的转录。在该研究中发现的这些元件之一,位于5'侧翼序列-147和-128之间,称为PED(正向远端元件),被发现对驱动编码TBP的基因的转录起重要的正向作用。在本报告中,我们以核苷酸水平分辨率绘制了构成PED的关键残基,纯化并测序与其结合的蛋白质,并确定该PED结合因子是Abf1p,一种先前广泛涉及基因调控和DNA复制的丰富酵母蛋白。然而,就编码TBP的基因而言,Abf1p通过作为非共有结合位点的PED元件起作用。根据其他人的工作,PED变体ABF1位点预计对该因子来说是一个非常差的结合位点,但Abf1p以相当的亲和力结合PED和共有ABF1位点。我们根据Abf1p介导的基因调控的更广泛背景讨论了这些结果。

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