Differentiation in the Gram-negative, aquatic bacterium C. crescentus, occurs as the direct result of asymmetric cell division to produce a nonmotile stalked cell and a new, motile swarmer cell. The differentiated surface structures that characterize the swarmer cell are assembled in the cell envelope at the incipient swarmer pole of the dividing stalked cell in a discrete temporal sequence during the cell cycle. These developmental events, which include flagellum biosynthesis, bacteriophage receptor formation, and pili formation, are triggered by internal signals originating from the cell division cycle. Successive stages of the cell division cycle are required as checkpoints for these developmental events. The long term goal of our studies is to decipher the genetic program that controls polar morphogenesis in Caulobacter. To achieve this, our work has focused primarily on the flagellum, whose assembly requires approximately 50 flagellar (fla) genes. These genes have been assigned to four classes (I-IV) within a regulatory hierarchy in which class I genes are at the top of the hierarchy and regulate transcription of class II-IV genes below. The focus of this proposal is to understand how the cell cycle regulates initiation of this transcriptional cascade and the molecular mechanisms that control transcriptional specificity within the cascade.
Our specific aims i nclude: l. Isolate sigma factors and regulatory proteins required for transcription from the class II promoters located near the top of the Caulobacter crescentus fla gene hierarchy. 2. Identify and isolate class I genes responsible for coupling initiation of fla gene transcriptional cascade to DNA replication in the cell cycle. 3. Examine the dependence of FlbD activity on other class II fla genes for the in vivo activation of class III and repression of class IIB genes. 4. Identify the mechanism that mediates the transition from expression of class III to class IV genes at the bottom of the fla gene hierarchy. We propose experiments based on genetic, molecular, and biochemical approaches to achieve these goals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM022299-24
Application #
2770893
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1978-09-01
Project End
2001-08-31
Budget Start
1998-09-01
Budget End
2001-08-31
Support Year
24
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Princeton University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Mullin, D A; Ohta, N; Mullin, A H et al. (2001) Organization, expression, and function of Caulobacter crescentus genes needed for assembly and function of the flagellar hook. Mol Genet Genomics 265:445-54
Wu, J; Ohta, N; Zhao, J L et al. (1999) A novel bacterial tyrosine kinase essential for cell division and differentiation. Proc Natl Acad Sci U S A 96:13068-73
Ward, D V; Newton, A (1999) Cell cycle expression and transcriptional regulation of DNA topoisomerase IV genes in caulobacter. J Bacteriol 181:3321-9
Wu, J; Ohta, N; Newton, A (1998) An essential, multicomponent signal transduction pathway required for cell cycle regulation in Caulobacter. Proc Natl Acad Sci U S A 95:1443-8
Wu, J; Newton, A (1997) The Caulobacter heat shock sigma factor gene rpoH is positively autoregulated from a sigma32-dependent promoter. J Bacteriol 179:514-21
Anderson, D K; Newton, A (1997) Posttranscriptional regulation of Caulobacter flagellin genes by a late flagellum assembly checkpoint. J Bacteriol 179:2281-8
Wu, J; Ohta, N; Benson, A K et al. (1997) Purification, characterization, and reconstitution of DNA-dependent RNA polymerases from Caulobacter crescentus. J Biol Chem 272:21558-64
Wu, J; Newton, A (1997) Regulation of the Caulobacter flagellar gene hierarchy; not just for motility. Mol Microbiol 24:233-9
Wu, J; Newton, A (1996) Isolation, identification, and transcriptional specificity of the heat shock sigma factor sigma32 from Caulobacter crescentus. J Bacteriol 178:2094-101
Anderson, D K; Ohta, N; Wu, J et al. (1995) Regulation of the Caulobacter crescentus rpoN gene and function of the purified sigma 54 in flagellar gene transcription. Mol Gen Genet 246:697-706

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