Cell-cell signaling controls many processes in the biological world, including development, pathogenesis, growth, mating, and transformation. Signaling processes are often mediated by factors (e.g. hormones, pheromones, neurotransmitters) that are produced by some cells and sensed by others. In bacteria, the ability to sense and respond to high population density is a type of cell-cell signaling often referred to as quorum-sensing. Cells produce extracellular signaling molecules that accumulate as population density increases, and a physiological response occurs at a critical density. The long-term goal of this project is to understand how Bacillus subtilis modulates gene expression and development in response to environmental conditions, with particular focus on aspects of peptide and cell-cell signaling. The major pathway for quorum sensing in B. subtilis involves activation of the transcription factor ComA, a response regulator that is active when phosphorylated. The activity of ComA is modulated by at least two different peptide signaling molecules that accumulate in culture supernatant as cells grow to high population density. A major challenge is to elucidate the range of cellular processes that are controlled by cell-cell signaling in a single species. This includes characterizing the genes that are regulated in response to population density, identifying the signaling molecules and pathways, and characterizing the web of overlapping interactions between responses to population density and other physiological signals. We will investigate these issues by characterizing the ComA-dependent quorum response, by characterizing other genes that are likely to be involved in cell-cell signaling, and by testing directly for and characterizing additional cell density-regulated responses. Central to this project is the use of DNA microarrays to characterize mRNA levels under a variety of conditions and in a variety of mutants. Our studies on quorum sensing and gene expression in B. subtilis, are relatively simple, experimentally accessible microbe should provide insights into general mechanisms of cell-cell signaling, signal transduction, and regulation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM050895-09
Application #
6681950
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Anderson, James J
Project Start
1994-05-01
Project End
2007-08-31
Budget Start
2003-09-01
Budget End
2004-08-31
Support Year
9
Fiscal Year
2003
Total Cost
$353,408
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Wright, Laurel D; Grossman, Alan D (2016) Autonomous Replication of the Conjugative Transposon Tn916. J Bacteriol 198:3355-3366
Johnson, Christopher M; Grossman, Alan D (2016) The Composition of the Cell Envelope Affects Conjugation in Bacillus subtilis. J Bacteriol 198:1241-9
Wright, Laurel D; Johnson, Christopher M; Grossman, Alan D (2015) Identification of a Single Strand Origin of Replication in the Integrative and Conjugative Element ICEBs1 of Bacillus subtilis. PLoS Genet 11:e1005556
Leonetti, Cori T; Hamada, Matt A; Laurer, Stephanie J et al. (2015) Critical Components of the Conjugation Machinery of the Integrative and Conjugative Element ICEBs1 of Bacillus subtilis. J Bacteriol 197:2558-67
Johnson, Christopher M; Grossman, Alan D (2015) Integrative and Conjugative Elements (ICEs): What They Do and How They Work. Annu Rev Genet 49:577-601
DeWitt, Tyler; Grossman, Alan D (2014) The bifunctional cell wall hydrolase CwlT is needed for conjugation of the integrative and conjugative element ICEBs1 in Bacillus subtilis and B. anthracis. J Bacteriol 196:1588-96
Johnson, Christopher M; Grossman, Alan D (2014) Identification of host genes that affect acquisition of an integrative and conjugative element in Bacillus subtilis. Mol Microbiol 93:1284-301
Thomas, Jacob; Lee, Catherine A; Grossman, Alan D (2013) A conserved helicase processivity factor is needed for conjugation and replication of an integrative and conjugative element. PLoS Genet 9:e1003198
Menard, Kayla L; Grossman, Alan D (2013) Selective pressures to maintain attachment site specificity of integrative and conjugative elements. PLoS Genet 9:e1003623
Kommineni, Sushma; Lama, Amrita; Popescu, Benjamin et al. (2012) Global transcriptional control by NsrR in Bacillus subtilis. J Bacteriol 194:1679-88

Showing the most recent 10 out of 39 publications