Novel protein-protein interaction between Escherichia coli SoxS and the DNA binding determinant of the RNA polymerase α subunit:: SoxS functions as a co-sigma factor and redeploys RNA polymerase from UP-element-containing promoters to SoxS-dependent promoters during oxidative stress

被引:42
作者
Shah, IM [1 ]
Wolf, RE [1 ]
机构
[1] Univ Maryland Baltimore Cty, Dept Biol Sci, Baltimore, MD 21228 USA
关键词
yeast two-hybrid system; SoxRS regulon; pre-recruitment; transcription activation; gene regulation;
D O I
10.1016/j.jmb.2004.08.057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SoxS is the transcription activator of the SoxRS regulon. Despite being synthesized de novo in response to oxidative stress and despite the large disparity between the number of SoxS binding sites and the number of SoxS molecules per cell, SoxS-dependent promoters are rapidly activated after the onset of the stress. With the usual recruitment/post-recruitment mechanisms being unsuitable for activating gene expression under these wconditions, we previously proposed that SoxS functions by "pre-recruitment". In pre-recruitment, SoxS forms SoxS-RNA polymerase binary complexes, which use the DNA binding properties of SoxS and sigma(70) to distinguish SoxS-dependent promoters from housekeeping promoters and from the large number of sequence equivalent but functionally irrelevant SoxS binding sites. With previous work in Escherichia coli having indicated that the most likely target on RNA polymerase for interaction with SoxS is the C-terminal domain of alpha, we investigated the interaction directly with the yeast two-hybrid system. We found that SoxS interacts with the alphaCTD and that SoxS positive control mutations disrupt the interaction. Moreover, single alanine substitutions of the alphaCTD that reduce or enhance SoxS activation in E. coli reduce or enhance the interaction between SoxS and the alphaCTD in yeast. Significantly, the critical amino acid residues lie in and around the DNA binding determinant of the alphaCTD, the first example of an activator contacting this determinant. These interactions were confirmed with an affinity immobilization assay. Lastly, we found that SoxS induction interferes with utilization of the UP element of an rRNA promoter. Thus, by functioning as a co-sigma factor that interacts with the DNA binding determinant of the alphaCTD, SoxS diverts RNA polymerase from UP-containing promoters to SoxS-activatable promoters. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:513 / 532
页数:20
相关论文
共 56 条
[11]   Bacterial promoter architecture:: subsite structure of UP elements and interactions with the carboxy-terminal domain of the RNA polymerase α subunit [J].
Estrem, ST ;
Ross, W ;
Gaal, T ;
Chen, ZWS ;
Niu, W ;
Ebright, RH ;
Gourse, RL .
GENES & DEVELOPMENT, 1999, 13 (16) :2134-2147
[12]   PURIFICATION OF A MALE-SOXS FUSION PROTEIN AND IDENTIFICATION OF THE CONTROL SITES OF ESCHERICHIA-COLI SUPEROXIDE-INDUCIBLE GENES [J].
FAWCETT, WP ;
WOLF, RE .
MOLECULAR MICROBIOLOGY, 1994, 14 (04) :669-679
[13]   DNA-binding determinants of the alpha subunit of RNA polymerase: Novel DNA-binding domain architecture [J].
Gaal, T ;
Ross, W ;
Blatter, EE ;
Tang, H ;
Jia, X ;
Krishnan, VV ;
AssaMunt, N ;
Ebright, RH ;
Gourse, RL .
GENES & DEVELOPMENT, 1996, 10 (01) :16-26
[14]   SoxR, a [2Fe-2S] transcription factor, is active only in its oxidized form [J].
Gaudu, P ;
Weiss, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10094-10098
[15]   Regulation of the soxRS oxidative stress regulon - Reversible oxidation of the Fe-S centers of SoxR in vivo [J].
Gaudu, P ;
Moon, N ;
Weiss, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :5082-5086
[16]   IMPROVED METHOD FOR HIGH-EFFICIENCY TRANSFORMATION OF INTACT YEAST-CELLS [J].
GIETZ, D ;
STJEAN, A ;
WOODS, RA ;
SCHIESTL, RH .
NUCLEIC ACIDS RESEARCH, 1992, 20 (06) :1425-1425
[17]  
Golemis EA, 1997, CURRENT PROTOCOLS MO, V3
[18]   UPs and downs in bacterial transcription initiation: the role of the alpha subunit of RNA polymerase in promoter recognition [J].
Gourse, RL ;
Ross, W ;
Gaal, T .
MOLECULAR MICROBIOLOGY, 2000, 37 (04) :687-695
[19]   Proteolytic degradation of Escherichia coli transcription activators SoxS and MarA as the mechanism for reversing the induction of the superoxide (SoxRS) and multiple antibiotic resistance (Mar) regulons [J].
Griffith, KL ;
Shah, IM ;
Wolf, RE .
MOLECULAR MICROBIOLOGY, 2004, 51 (06) :1801-1816
[20]   A comprehensive alanine scanning mutagenesis of the Escherichia coli transcriptional activator SoxS:: Identifying amino acids important for DNA binding and transcription activation [J].
Griffith, KL ;
Wolf, RE .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 322 (02) :237-257