My goal is to understand the systematic modulation of gene expression in response to problems duringDNA replication. Failure to complete DMA replication in a timely manner can lead to cell death or genomeinstability, often associated with cancer. In many organisms, the effects of DNA damage and other causesof distress during replication are often mitigated through transcriptional responses. Recently, a novel globaltranscriptional response was identified in a functional genomic analysis of Bacillus subtilis cells perturbed inDNA replication. At least 50 of these genes are thought to be regulated by DnaA, an essential and wellconserved ATPase, transcription factor, and replication initiator. I plan to identify the genes directlyregulated by DnaA in B. subtilis, address how DnaA is activated as a transcriptional regulator, and examinehow its target promoters are structured to respond to it.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM076950-03
Application #
7320656
Study Section
Special Emphasis Panel (ZRG1-F08 (20))
Program Officer
Portnoy, Matthew
Project Start
2005-12-01
Project End
2008-08-31
Budget Start
2007-12-01
Budget End
2008-08-31
Support Year
3
Fiscal Year
2008
Total Cost
$39,571
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