Cell differentiation is a fundamental biological process. Central to it are the establishment of distinct programs of gene expression in the different cell types and the coordination of gene expression with morphological change. Formation of spores by Bacillus subtilis is a primitive system of cell differentiation that has become a paradigm for the study of cell differentiation in prokaryotes because of the ease of its genetic manipulation. All the key regulators of spore formation are also identified in all sequenced species of Bacillaceae, including the pathogens Bacillus anthracis and Clostridium difficile. Sporulation involves a characteristic division into two distinct cell types, the mother cell and the prespore. The prespore is engulfed by the mother cell and develops into the mature, resistant spore. Sporulation requires the action of four RNA polymerase sigma factors, sigmaF and then sigmaG in the prespore and sigmaE and then in sigmak the mother cell. The major objectives here are to understand how compartmentalized gene expression is established and maintained and how gene expression is coordinated with morphological change. Most of the proposal centers on B. subtilis. A series of interconnected lines of research will be pursued. It is proposed to investigate why sigmaG activity switches from the prespore to the mother cell in spollAdelta mutants. It is proposed to identify and characterize division genes and regulators of sF activation that are required for prespore-specific expression using a two-part compartmentalization test we have developed. It is proposed to investigate why certain sF-directed genes are poorly expressed when they are relocated near the chromosome terminus. It is proposed to identify and characterize genes involved in temporal control of sigmaF and sigmaG activity. It is proposed to investigate the establishment of compartmentalization in Sporosarcina ureae where the sporulation division is medially located, in contrast to its grossly asymmetric location for species of Bacillus and Clostridium.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM043577-18
Application #
6840387
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Anderson, James J
Project Start
1986-07-01
Project End
2007-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
18
Fiscal Year
2005
Total Cost
$361,200
Indirect Cost
Name
Temple University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
057123192
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
Regan, Genevieve; Itaya, Mitsuhiro; Piggot, Patrick J (2012) Coupling of ýýG activation to completion of engulfment during sporulation of Bacillus subtilis survives large perturbations to DNA translocation and replication. J Bacteriol 194:6264-71
Xenopoulos, Panagiotis; Piggot, Patrick J (2011) Regulation of growth of the mother cell and chromosome replication during sporulation of Bacillus subtilis. J Bacteriol 193:3117-26
Chary, Vasant K; Xenopoulos, Panagiotis; Eldar, Avigdor et al. (2010) Loss of compartmentalization of ?(E) activity need not prevent formation of spores by Bacillus subtilis. J Bacteriol 192:5616-24
Eldar, Avigdor; Chary, Vasant K; Xenopoulos, Panagiotis et al. (2009) Partial penetrance facilitates developmental evolution in bacteria. Nature 460:510-4
Chary, Vasant K; Xenopoulos, Panagiotis; Piggot, Patrick J (2006) Blocking chromosome translocation during sporulation of Bacillus subtilis can result in prespore-specific activation of sigmaG that is independent of sigmaE and of engulfment. J Bacteriol 188:7267-73
Chary, V K; Hilbert, D W; Higgins, M L et al. (2000) The putative DNA translocase SpoIIIE is required for sporulation of the symmetrically dividing coccal species Sporosarcina ureae. Mol Microbiol 35:612-22
Schuch, R; Piggot, P J (1994) The dacF-spoIIA operon of Bacillus subtilis, encoding sigma F, is autoregulated. J Bacteriol 176:4104-10
Bylund, J E; Zhang, L; Haines, M A et al. (1994) Analysis by fluorescence microscopy of the development of compartment-specific gene expression during sporulation of Bacillus subtilis. J Bacteriol 176:2898-905
Birkey, S M; Sun, G; Piggot, P J et al. (1994) A pho regulon promoter induced under sporulation conditions. Gene 147:95-100
Moldover, B; Cao, L; Piggot, P J (1994) Identification of a control region for expression of the forespore-specific Bacillus subtilis locus spoVA. Microbiology 140 ( Pt 9):2299-304

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