Fundamental to all cells is the ability to alter the pattern of gene expression in response to environmental and metabolic signals. In prokaryotes most signal transduction and stress response systems ultimately act at the transcriptional level to express sets of genes needed to adapt to changing conditions. Our experimental focus is the role of RNA polymerase in controlling stationary phase gene expression in the Gram positive bacterium Bacillus subtilis. This analysis will contribute to understanding the functions, interactions, and regulation of the transcriptional machinery of a model developmental system, including the RNA polymerase catalytic core, the sigma factors that determine promoter recognition, and interacting accessory factors. Bacillus subtilis cells manifest diverse responses in stationary phase, including expression of genes important for transition to the non-growing state, initiation of the sporulation process, development of genetic competence, and production of extracellular enzymes and antibiotics. Alternative sigma factors have a central role in coordinating these stationary phase events. Thus it is important to understand the molecular mechanisms that regulate sigma factor activity and interaction with the RNA polymerase core enzyme. The primary goal of this proposal is to investigate the physiological role and regulation of sigma-B, an alternative sigma factor implicated in stationary phase stress response. A combined biochemical and genetic approach will address the following questions: (l) What stationary phase genes are controlled by sigma-B, and how is their expression regulated; (2) What are the molecular mechanisms controlling sigma-B activity in response to stationary phase signals; (3) How do sigma-B and other dispensable sigma factors interact with RNA polymerase core; and, in an extension of this process, (4) What developmental functions are mediated by genes directly controlled by the stationary phase transcription factor sigma-F? Specific aspects of this research will be directly relevant to understanding stationary phase regulation in a broad range of bacteria, including antibiotic biosynthesis by Streptomyces species and the production of virulence factors by bacterial pathogens. The problem of ordered regulation of gene expression in response to environmental, metabolic, and morphological signals is common in biology, and the biochemical principles that govern sigma factor regulation and interaction with RNA polymerase are likely relevant to proteins that associate with RNA polymerases in all organisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042077-11
Application #
2181212
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1988-08-01
Project End
1997-07-31
Budget Start
1995-08-01
Budget End
1996-07-31
Support Year
11
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of California Davis
Department
Nutrition
Type
Schools of Earth Sciences/Natur
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Gaidenko, Tatiana A; Price, Chester W (2014) Genetic evidence for a phosphorylation-independent signal transduction mechanism within the Bacillus subtilis stressosome. PLoS One 9:e90741
Gaidenko, Tatiana A; Bie, Xiaomei; Baldwin, Enoch P et al. (2012) Two surfaces of a conserved interdomain linker differentially affect output from the RST sensing module of the Bacillus subtilis stressosome. J Bacteriol 194:3913-21
Eymann, Christine; Schulz, Stephan; Gronau, Katrin et al. (2011) In vivo phosphorylation patterns of key stressosome proteins define a second feedback loop that limits activation of Bacillus subtilis ýýB. Mol Microbiol 80:798-810
Gaidenko, Tatiana A; Bie, Xiaomei; Baldwin, Enoch P et al. (2011) Substitutions in the presumed sensing domain of the Bacillus subtilis stressosome affect its basal output but not response to environmental signals. J Bacteriol 193:3588-97
Nadezhdin, Eugene V; Brody, Margaret S; Price, Chester W (2011) An ýý/ýý hydrolase and associated Per-ARNT-Sim domain comprise a bipartite sensing module coupled with diverse output domains. PLoS One 6:e25418
Shin, Ji-Hyun; Brody, Margaret S; Price, Chester W (2010) Physical and antibiotic stresses require activation of the RsbU phosphatase to induce the general stress response in Listeria monocytogenes. Microbiology 156:2660-9
Brody, Margaret S; Stewart, Valley; Price, Chester W (2009) Bypass suppression analysis maps the signalling pathway within a multidomain protein: the RsbP energy stress phosphatase 2C from Bacillus subtilis. Mol Microbiol 72:1221-34
Shin, Ji-Hyun; Price, Chester W (2007) The SsrA-SmpB ribosome rescue system is important for growth of Bacillus subtilis at low and high temperatures. J Bacteriol 189:3729-37
Igoshin, Oleg A; Brody, Margaret S; Price, Chester W et al. (2007) Distinctive topologies of partner-switching signaling networks correlate with their physiological roles. J Mol Biol 369:1333-52
Gaidenko, Tatiana A; Kim, Tae-Jong; Weigel, Andrea L et al. (2006) The blue-light receptor YtvA acts in the environmental stress signaling pathway of Bacillus subtilis. J Bacteriol 188:6387-95

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