It is the long-term goal of this research proposal to determine how the rate of DNA replication is coordinated to the cell division cycle in the model organism of E. coli. Understanding these events in bacteria is essential to guide future cell-cycle research in humans. To achieve this goal, this research project is designed to resolve two questions about replication control in e. COLI: First, what is the role of SeqA protein in regulating initiation of DNA replication, and specifically, what is its role in controlling origin movement within the cell? Second, what is the relationship between the sequence of events occurring at replication termiantion in part controlled by SeqA, and the timing of replication initiation? These questions will be addressed by examining the timing of varius events, by fluorescence microscopy and molecular methods, that occur at and immediately and mutant cells that are defective in the control of replication initiation. In the process of this investigation, we will develop a new method to obtain synchronized cultures.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM020627-01
Application #
6208152
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Tompkins, Laurie
Project Start
2000-09-01
Project End
Budget Start
2000-09-01
Budget End
2001-08-31
Support Year
1
Fiscal Year
2000
Total Cost
$32,416
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Stepankiw, Nicholas; Kaidow, Akihiro; Boye, Erik et al. (2009) The right half of the Escherichia coli replication origin is not essential for viability, but facilitates multi-forked replication. Mol Microbiol 74:467-79
Bates, David (2008) The bacterial replisome: back on track? Mol Microbiol 69:1341-8