LexA repressor of E. coli plays a central role in regulation of the SOS response to DNA damage. LexA represses a set of about 20 genes during normal growth. After DNA damage, RecA protein is activated to a form that mediates cleavage of LexA. Cleavage inactivates LexA, leading to derepression of the SOS regulon. The basis for the proposed work is the crystal structures of several mutant LexA proteins. Two forms of LexA are observed. In the NC form, the cleavage site is distant from the active site. In the C form, the cleavage site lies in the active site and is adjacent to the nucleophile that attacks the peptide bond. It is proposed to use the structures as a guide for further analysis of several LexA functions. First, the model will be tested that these forms represent the mechanism controlling reactivity of LexA. Mutants will be made that are predicted to stabilize the C form, and their cleavage rates will be tested. Interesting proteins will be analyzed by x-ray crystallography. Second, dimerization mutants will be made and characterized. Third, in order to characterize further the chemical mechanism of LexA cleavage, efforts will be made to develop a simple substrate for this reaction, and to isolate a covalent intermediate. Fourth, the model will be tested that other cleavable proteins in the LexA superfamily, notably UmuD and lambda repressor, have the same mechanism for controlling their cleavage reactions. Fifth, the structure will be used as a guide to identify portions of LexA involved in interaction with activated RecA. RecA-mediated cleavage will be analyzed in more detail. Efforts will be made to solve the structure of a RecA:LexA complex.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM065180-04
Application #
7039163
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Lewis, Catherine D
Project Start
2002-04-01
Project End
2010-03-31
Budget Start
2006-04-01
Budget End
2010-03-31
Support Year
4
Fiscal Year
2006
Total Cost
$257,198
Indirect Cost
Name
University of Arizona
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Giese, Kim C; Michalowski, Christine B; Little, John W (2008) RecA-dependent cleavage of LexA dimers. J Mol Biol 377:148-61