Initiation of Escherichia coli chromosomal replication is a key event in the bacterial growth cycle. The long term objectives of this proposed research are to obtain a biochemical understanding of the initiation of DNA replication and its coordination to cell growth. dnaA protein plays a central role in the initiation process and appears to determine the time in the bacterial cell cycle when initiation of replication occurs. This protein also appears to synchronize this process at multiple replication origins in a rapidly growing cell, and regulates the expression of its own gene and of several other genes of e. coli. One approach to further understanding of the role of dnaA protein in E coli is by the production and analysis of mutant forms of dnaA protein in comparison with its wild type counterpart. The second involves the interaction of mutant forms of dnaA protein with dnaK, grpE, and dnaJ heat shock proteins which appear to influence replication activity and may represent a mechanism for regulation of the initiation process. The third approach involves correlation of structural domains of dnaA protein to its various activities by use of monoclonal antibodies and by site-specific mutagenesis. While this research addresses a basic biochemical problem such findings may be useful in understanding the mechanism of chromosomal replication and its regulation in higher organisms. These findings may be useful in the design of agents which promote or interfere with cell growth in plants and animals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033992-09
Application #
3284295
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1984-07-01
Project End
1995-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
9
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
Schools of Arts and Sciences
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Makowska-Grzyska, Magdalena; Kaguni, Jon M (2010) Primase directs the release of DnaC from DnaB. Mol Cell 37:90-101
Felczak, Magdalena M; Kaguni, Jon M (2009) DnaAcos hyperinitiates by circumventing regulatory pathways that control the frequency of initiation in Escherichia coli. Mol Microbiol 72:1348-63