Sigma factors are bacterial transcription initiation factors, which bind to the bacterial """"""""core"""""""" RNA polymerase and impart on the resulting """"""""holo"""""""" RNA polymerase the ability to recognize promoter DNA sequences and orchestrate the strand separation of promoter DNA required for establishment of the initiation-competent """"""""open"""""""" RNA polymerase-promoter complex. The focus of this application is on the role of sigma factor in formation of the open complex. With initiation of RNA synthesis being the major point of regulation of gene expression, the biological relevance of our studies stems from the insights into this process that our work will provide. ? ? We had previously demonstrated that particular aromatic and basic residues in conserved region 2.3 of the main sigma factor of E. coli, sigma70, were crucial to the DNA strand separation process. We proposed that these residues initiated strand separation by facilitating the rotation of the -11A of the promoter out of the DNA helix and into a binding pocket on RNA polymerase. This model will be further tested by using fluorescence techniques. ? ? In studies on sigma32, the heat shock sigma factor of E. coli, and sigmaA, the main sigma factor of the thermophilic bacterium, T. aquaticus, we will explore the generality of the principles established for sigma70, with emphasis on the DNA melting function of region 2.3. In this region, sigmaA is almost identical to sigma70, but sigma32 is different at about half the amino acid residues. The importance of residues in region 2.3 will be assessed by determining the effects of alanine substitutions on open complex formation and on the interaction of RNA polymerase with several model DNAs. We will also develop a single-molecule assay for the interaction of RNA polymerase with promoter DNA, which should allow intermediate promoter complexes to be more readily detected and characterized than possible with current techniques. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM031808-20A1
Application #
6779258
Study Section
Special Emphasis Panel (ZRG1-MBC-2 (01))
Program Officer
Tompkins, Laurie
Project Start
1983-04-01
Project End
2008-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
20
Fiscal Year
2004
Total Cost
$367,200
Indirect Cost
Name
Case Western Reserve University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Saecker, Ruth M; Record Jr, M Thomas; Dehaseth, Pieter L (2011) Mechanism of bacterial transcription initiation: RNA polymerase - promoter binding, isomerization to initiation-competent open complexes, and initiation of RNA synthesis. J Mol Biol 412:754-71
Schroeder, Lisa A; Gries, Theodore J; Saecker, Ruth M et al. (2009) Evidence for a tyrosine-adenine stacking interaction and for a short-lived open intermediate subsequent to initial binding of Escherichia coli RNA polymerase to promoter DNA. J Mol Biol 385:339-49
Koo, Byoung-Mo; Rhodius, Virgil A; Nonaka, Gen et al. (2009) Reduced capacity of alternative sigmas to melt promoters ensures stringent promoter recognition. Genes Dev 23:2426-36
Schroeder, Lisa A; Karpen, Mary E; deHaseth, Pieter L (2008) Threonine 429 of Escherichia coli sigma 70 is a key participant in promoter DNA melting by RNA polymerase. J Mol Biol 376:153-65
Cook, Victoria M; Dehaseth, Pieter L (2007) Strand opening-deficient Escherichia coli RNA polymerase facilitates investigation of closed complexes with promoter DNA: effects of DNA sequence and temperature. J Biol Chem 282:21319-26
Schroeder, Lisa A; Choi, Ae-Jin; DeHaseth, Pieter L (2007) The -11A of promoter DNA and two conserved amino acids in the melting region of sigma70 both directly affect the rate limiting step in formation of the stable RNA polymerase-promoter complex, but they do not necessarily interact. Nucleic Acids Res 35:4141-53
Kourennaia, Olga V; Dehaseth, Pieter L (2007) Substitution of a highly conserved histidine in the Escherichia coli heat shock transcription factor, sigma32, affects promoter utilization in vitro and leads to overexpression of the biofilm-associated flu protein in vivo. J Bacteriol 189:8430-6
Schroeder, Lisa A; deHaseth, Pieter L (2005) Mechanistic differences in promoter DNA melting by Thermus aquaticus and Escherichia coli RNA polymerases. J Biol Chem 280:17422-9
Kourennaia, Olga V; Tsujikawa, Laura; Dehaseth, Pieter L (2005) Mutational analysis of Escherichia coli heat shock transcription factor sigma 32 reveals similarities with sigma 70 in recognition of the -35 promoter element and differences in promoter DNA melting and -10 recognition. J Bacteriol 187:6762-9
Sun, Li; Dove, Simon L; Panaghie, Gianina et al. (2004) An RNA polymerase mutant deficient in DNA melting facilitates study of activation mechanism: application to an artificial activator of transcription. J Mol Biol 343:1171-82

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