Stable DNA opening within open promoter complexes is mediated by the RNA polymerase β′-jaw domain

被引:20
作者
Wigneshweraraj, SR
Burrows, PC
Severinov, K
Buck, M
机构
[1] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
[2] Univ London Imperial Coll Sci Technol & Med, Fac Life Sci, Div Biol, London SW7 2AZ, England
[3] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
[4] Russian Acad Sci, Inst Mol Genet, Moscow 123182, Russia
关键词
D O I
10.1074/jbc.M506416200
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
DNA opening for transcription-competent open promoter complex (OC) formation by the bacterial RNA polymerase ( RNAP) relies upon a complex network of interactions between the structurally conserved and flexible modules of the catalytic beta and beta'-subunits, RNAP-associated sigma-subunit, and the DNA. Here, we show that one such module, the beta'-jaw, functions to stabilize the OC. In OCs formed by the major sigma(70)-RNAP, the stabilizing role of the beta'-jaw is not restricted to any particular melted DNA segment. In contrast, in OCs formed by the major variant sigma(54)-RNAP, the beta'-jaw and a conserved sigma(54) regulatory domain co-operate to stabilize the melted DNA segment immediately upstream of the transcription start site. Clearly, regulated communication between the mobile modules of the RNAP and the functional domain(s) of the sigma subunit is required for stable DNA opening.
引用
收藏
页码:36176 / 36184
页数:9
相关论文
共 35 条
[1]   Communication between Eσ54, promoter DNA and the conserved threonine residue in the GAFTGA motif of the PspF σ54-dependent activator during transcription activation [J].
Bordes, P ;
Wigneshweraraj, SR ;
Chaney, M ;
Dago, AE ;
Morett, E ;
Buck, M .
MOLECULAR MICROBIOLOGY, 2004, 54 (02) :489-506
[2]   The bacterial enhancer-dependent σ54 (σN) transcription factor [J].
Buck, M ;
Gallegos, MT ;
Studholme, DJ ;
Guo, YL ;
Gralla, JD .
JOURNAL OF BACTERIOLOGY, 2000, 182 (15) :4129-4136
[3]   Reorganisation of an RNA polymerase-promoter DNA complex for DNA melting [J].
Burrows, PC ;
Severinov, K ;
Buck, M ;
Wigneshweraraj, SR .
EMBO JOURNAL, 2004, 23 (21) :4253-4263
[4]   Mapping σ54-RNA polymerase interactions at the -24 consensus promoter element [J].
Burrows, PC ;
Severinov, K ;
Ishihama, A ;
Buck, M ;
Wigneshweraraj, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29728-29743
[5]   Structural basis of transcription: An RNA polymerase II-TFIIB cocrystal at 4.5 angstroms [J].
Bushnell, DA ;
Westover, KD ;
Davis, RE ;
Kornberg, RD .
SCIENCE, 2004, 303 (5660) :983-988
[6]   IDENTIFICATION OF CLOSE CONTACTS BETWEEN THE SIGMA(N) (SIGMA(54)) PROTEIN AND PROMOTER DNA IN CLOSED PROMOTER COMPLEXES [J].
CANNON, W ;
AUSTIN, S ;
MOORE, M ;
BUCK, M .
NUCLEIC ACIDS RESEARCH, 1995, 23 (03) :351-356
[7]   Amino-terminal sequences of σN (σ54) inhibit RNA polymerase isomerization [J].
Cannon, W ;
Gallegos, MT ;
Casaz, P ;
Buck, M .
GENES & DEVELOPMENT, 1999, 13 (03) :357-370
[8]   DNA melting within a binary σ54-promoter DNA complex [J].
Cannon, W ;
Gallegos, MT ;
Buck, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (01) :386-394
[9]  
Cannon WV, 2000, NAT STRUCT BIOL, V7, P594
[10]   Systematic analysis of σ54 N-terminal sequences identifies regions involved in positive and negative regulation of transcription [J].
Casaz, P ;
Gallegos, MT ;
Buck, M .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (02) :229-239