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 order to understand regulatory process involving cell-cell signaling, it is essential to identify the signaling molecules, determine how they are produced and sensed, and determine how the signals are transduced to elicit a regulatory response. The long term goal of this project is to understand how cell-cell signaling controls gene expression and differentiation in Bacillus subtilis. B. subtilis produces extracellular signaling molecules that are at least in part oligopeptides that accumulate in culture medium as cells grow to high density. These extracellular signaling peptides stimulate expression of genes needed for the development of genetic competence. Genetic competence in B. subtilis is the natural ability to be transformed by exogenous DNA and is an efficient means of genetic exchange.
Our aims are to purify and biochemically characterize the signaling molecules that induce competence gene expression and competence, to characterize how these extracellular signaling molecules are produced, to characterize the mechanisms by which cells sense and respond to these peptide factors, and to determine if the signaling factors involved in competence also affect sporulation. Included in these aims is to characterize the role of the spoOK (opp) operon in the cellular response to peptide signaling factors. Mutations in spoOK cause a defect in competence (and sporulation) and prevent cells from responding to the peptide signaling molecules that stimulate competence gene expression. spoOK encodes an oligopeptide permease that is a member of the large family of ATP-dependent transporters. This family of transport systems includes MDR, involved in multi-drug resistance, CFTR, the cystic fibrosis transmembrane regulator, and Hly, required for hemolysin export in some pathogenic bacteria. Also included in this family of transporters are a variety of permeases from bacteria that mediate uptake of many compounds, including histidine, maltose, phosphate, dipeptides, vitamin B 12, and iron. An important aim of this proposal is to determine how the oligopeptide Permease encoded by spoOK of B. subtilis is involved in controlling expression of competence genes. Our studies on differentiation in this relatively simple, experimentally accessible microbe should provide insights into general mechanisms of cell-cell signaling, signal transduction, and regulation of gene expression and differentiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM050895-01
Application #
2189065
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1994-05-01
Project End
1998-04-30
Budget Start
1994-05-01
Budget End
1995-04-30
Support Year
1
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
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

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