The mechanism(s) used to control the timing and frequency of replication initiation in Gram positive bacteria are unknown. YabA is a negative regulator of replication initiation in B. subtilis, and is conserved in other Gram positive bacteria. The mechanism by which YabA carries out its regulatory function is not yet understood. I found that YabA associates with the chromosomal origin of replication (oriC), and is delivered there at a step following the loading of the replicative helicase. I propose a series of experiments to identify the factor(s) necessary for association of YabA with oriC. I also propose experiments to determine if the subcellular location of YabA and its association with the chromosome changes during the replication cycle. These experiments should provide insights into the timing of YabA's function in inhibition of replication initiation. Finally, I propose several in vivo and in vitro experiments to determine the mechanism of inhibition of replication initiation by YabA.

Public Health Relevance

Regulation of DNA replication is critical for survival and growth, and is generally achieved by controlling the timing and frequency of replication initiation. The mechanisms behind this kind of control remain elusive in a large subset of bacteria known as Gram-positives, a subgroup of which contribute to pathogenesis and human disease. The goal of this project is to study one of the mechanisms behind DNA replication control, and the results of this proposal could contribute to better understanding of these processes, as well as provide general insights into replication control in pathogenic bacteria.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM093408-01
Application #
7908241
Study Section
Special Emphasis Panel (ZRG1-F08-E (20))
Program Officer
Hagan, Ann A
Project Start
2010-04-01
Project End
2013-03-31
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
1
Fiscal Year
2010
Total Cost
$47,606
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
Merrikh, Houra; Zhang, Yan; Grossman, Alan D et al. (2012) Replication-transcription conflicts in bacteria. Nat Rev Microbiol 10:449-58
Merrikh, Houra; Grossman, Alan D (2011) Control of the replication initiator DnaA by an anti-cooperativity factor. Mol Microbiol 82:434-46
Merrikh, Houra; Machón, Cristina; Grainger, William H et al. (2011) Co-directional replication-transcription conflicts lead to replication restart. Nature 470:554-7
Rahn-Lee, Lilah; Merrikh, Houra; Grossman, Alan D et al. (2011) The sporulation protein SirA inhibits the binding of DnaA to the origin of replication by contacting a patch of clustered amino acids. J Bacteriol 193:1302-7
Smits, Wiep Klaas; Merrikh, Houra; Bonilla, Carla Yaneth et al. (2011) Primosomal proteins DnaD and DnaB are recruited to chromosomal regions bound by DnaA in Bacillus subtilis. J Bacteriol 193:640-8