The products of genes ntrA, ntrB, and ntrC are required for nitrogen-regulated transcription in enteric bacteria. The product of gene ntrA (called NTRA) is an alternate sigma subunit for RNA polymerase: NTRA plus core RNA polymerase (referred to as NTRA holoenzyme) can bind to a """"""""strong"""""""" nitrogen-regulated promoter in the absence of other factors. The ntrC product (called NTRC), which is a DNA binding protein, is required for efficient initiation of transcription by NTRA holoenzyme. Binding sites for NTRC in two nitrogen-regulated promoter regions lie 100-150bp upstream of the promoter (76,101) and appear to resemble transcriptional enhancers in eukaryotes (76). To activate transcription NTRC must be phosphorylated. It is phosphorylated--and dephosphorylated--by the product of the ntrB gene (NTRB), which is a bifunctional protein kinase- phosphoprotein phosphatase (69,50). The degee of phosphorylation of NTRC is metabolically regulated. Metabolic regulation controls the activities of the bifunctional enzyme NTRB and involves at least two additional proteins, one of which appears to be a primary sensor of the status of cellular nitrogen nutrition. We will undertake biochemical studies and a structure-function analysis of NTRC in order to determine the precise mechanism by which this enhancer activating protein stimulates initiation of transcription. We will also perform a structure-function analysis of the sigma factor NTRA to determine the nature of its interactions with NTRC, core polymerase and promoter DNA. These studies will be facilitated by the fact that NTRA is not essential for cell viability. Finally, we will study in detail the nature of metabolic controls of NTRB activity by other proteins and by small molecules. Our eventual goal in this regard is to determine whether pool sizes of the metabolites glutamine and 2- oxoglutarate correlate directly with rates of transcription by NTC and NTRA holoenzyme and, if so, the extent to which these pool sizes must vary to give the full physiological range of transcription rates.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM038361-06
Application #
3294777
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1986-09-15
Project End
1993-05-31
Budget Start
1991-06-01
Budget End
1992-05-31
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Hall, Jason A; Yan, Dalai (2013) The molecular basis of K+ exclusion by the Escherichia coli ammonium channel AmtB. J Biol Chem 288:14080-6
Vo, Jason; Inwood, William; Hayes, John M et al. (2013) Mechanism for nitrogen isotope fractionation during ammonium assimilation by Escherichia coli K12. Proc Natl Acad Sci U S A 110:8696-701
Kim, Minsu; Zhang, Zhongge; Okano, Hiroyuki et al. (2012) Need-based activation of ammonium uptake in Escherichia coli. Mol Syst Biol 8:616
Hall, Jason A; Kustu, Sydney (2011) The pivotal twin histidines and aromatic triad of the Escherichia coli ammonium channel AmtB can be replaced. Proc Natl Acad Sci U S A 108:13270-4
Kim, Kwang-Seo; Pelton, Jeffrey G; Inwood, William B et al. (2010) The Rut pathway for pyrimidine degradation: novel chemistry and toxicity problems. J Bacteriol 192:4089-102
Inwood, William B; Hall, Jason A; Kim, Kwang-Seo et al. (2009) Epistatic effects of the protease/chaperone HflB on some damaged forms of the Escherichia coli ammonium channel AmtB. Genetics 183:1327-40
Inwood, William B; Hall, Jason A; Kim, Kwang-Seo et al. (2009) Genetic evidence for an essential oscillation of transmembrane-spanning segment 5 in the Escherichia coli ammonium channel AmtB. Genetics 183:1341-55
Inwood, William; Yoshihara, Corinne; Zalpuri, Reena et al. (2008) The ultrastructure of a Chlamydomonas reinhardtii mutant strain lacking phytoene synthase resembles that of a colorless alga. Mol Plant 1:925-37
Yoshihara, Corinne; Inoue, Kentaro; Schichnes, Denise et al. (2008) An Rh1-GFP fusion protein is in the cytoplasmic membrane of a white mutant strain of Chlamydomonas reinhardtii. Mol Plant 1:1007-20
Yan, Dalai (2007) Protection of the glutamate pool concentration in enteric bacteria. Proc Natl Acad Sci U S A 104:9475-80

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