Regulation of gene expression in Borrelia burgdorferi
Project Number5R01AI051486-04
Contact PI/Project LeaderSAMUELS, D. SCOTT
Awardee OrganizationUNIVERSITY OF MONTANA
Description
Abstract Text
DESCRIPTION (provided by applicant): The bacterium Borrelia burgdorferi is a causative agent of Lyme disease. B. burgdorferi can synthesize several different outer surface proteins that are involved in pathogenesis or transmission during the enzootic cycle. The regulation of outer surface protein synthesis is not well understood at the molecular level. This application proposes to evaluate the hypothesis that cis-acting factors, such as DNA supercoiling, and trans-acting factors, such as DNA-binding repressor proteins, regulate the expression of outer surface protein genes in response to environmental signals. Production of outer surface proteins OspA and OspC is reciprocally regulated, which may be how B. burgdorferi adapts to the different environments of the tick vector and mammalian host or effects transmission between the environments. An ospAB operon promoter-specific trans-acting protein is hypothesized to repress ospAB transcription. The regulatory protein will be purified and identified. Cis-acting sequences in the ospAB promoter region are hypothesized to mediate transcriptional regulation. These sites will be mapped and characterized. The architectural DNA-binding protein Hbb is hypothesized to facilitate regulation of ospC expression. The function of Hbb will be probed by mutagenesis of the hbb gene and the Hbb binding site in the ospC promoter region. The ospC promoter will be replaced with an inducible promoter system to control cellular OspC levels without perturbing DNA supercoiling so that the coupling of ospC and ospAB transcription can be studied. ospC gene expression from the flac hybrid promoter is hypothesized to be regulated by IPTG and to influence ospAB operon expression. The mechanism by which DNA supercoiling regulates ospC expression is hypothesized to involve Hbb and specific sequence motifs in the ospC promoter region. Mutant ospC promoters will be constructed. The transcriptional response of these mutants to temperature and DNA supercoiling will be assayed in order to define the cis-acting elements responsible for regulation. The long-term objective of these studies is to understand the mechanism of outer surface protein gene regulation in response to environmental signals.
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
010379790
UEI
DAY7Z8ZD48Q3
Project Start Date
05-September-2003
Project End Date
31-December-2007
Budget Start Date
01-January-2006
Budget End Date
31-December-2006
Project Funding Information for 2006
Total Funding
$338,160
Direct Costs
$244,125
Indirect Costs
$94,035
Year
Funding IC
FY Total Cost by IC
2006
National Institute of Allergy and Infectious Diseases
$338,160
Year
Funding IC
FY Total Cost by IC
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