Faulty DNA repair can promote mutations, aging, cancer and cell death. The process by which protein components of repair detect damaged or modified bases within DNA is an important, but poorly understood type of protein-DNA interaction. One of the most remarkable aspects of nucleotide excision repair (NER) is that it can remove a wide range of DNA lesions that differ in chemistry and structure. During bacterial NER UvrA, UvrB, and UvrC proteins work together to identify and remove DNA damage. The UvrA and UvrB proteins are believed to recognize damage-induced distortion in the DNA helix rather than the lesion per se. However, detailed studies of the kinetics, thermodynamics and structures of the Uvr proteins have been limited due to their instability. To overcome this problem we recently cloned and overexpressed UvrA, UvrB and UvrC from the thermophilic bacteria, Bacillus caldotenax and Thermotoga maritima. The proteins maintain optimal activity at 65 ?C and are amenable to both structural and biophysical studies. We are collaborating with Dr. Bob London?s group (NIEHS) for an analysis of the dynamics of UvrB upon ligand binding using NMR techniques. We are also collaborating with Dr. Caroline Kisker?s group (Wourtzburg, Germany) on solving protein and protein-DNA structures by X-ray crystallography. Combined with site-directed mutagenesis and biochemical analyses, these structure-function studies of the UvrA, UvrB, and UvrC proteins form a basis for understanding the fundamental molecular processes of NER. Our long-term goal is to have a complete understanding of how structural perturbations induced by specific DNA lesions are detected and removed by the NER machinery at the atomic level. We are also performing a series of studies on the formation and repair of UVC damage in an entire multi-celled eukaryotic organism, Caenorhabditis elegans. This organism contains the entire complement of NER proteins that are homologous to humans. In collaboration with Drs. Boyd and Freedman (NIEHS) analysis with specific mutations and RNAi knock-down technology allows a global assessment of the effect of DNA damage on the life and biology of the organism.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Intramural Research (Z01)
Project #
1Z01ES061060-08
Application #
7328448
Study Section
(LMG)
Project Start
Project End
Budget Start
Budget End
Support Year
8
Fiscal Year
2006
Total Cost
Indirect Cost
Name
U.S. National Inst of Environ Hlth Scis
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Wang, Hong; Tessmer, Ingrid; Croteau, Deborah L et al. (2008) Functional characterization and atomic force microscopy of a DNA repair protein conjugated to a quantum dot. Nano Lett 8:1631-7
Wolski, Stefanie C; Kuper, Jochen; Hanzelmann, Petra et al. (2008) Crystal structure of the FeS cluster-containing nucleotide excision repair helicase XPD. PLoS Biol 6:e149
Imoto, Shuhei; Bransfield, Leslie A; Croteau, Deborah L et al. (2008) DNA tandem lesion repair by strand displacement synthesis and nucleotide excision repair. Biochemistry 47:4306-16
Croteau, Deborah L; DellaVecchia, Matthew J; Perera, Lalith et al. (2008) Cooperative damage recognition by UvrA and UvrB: identification of UvrA residues that mediate DNA binding. DNA Repair (Amst) 7:392-404
Croteau, Deborah L; Peng, Ye; Van Houten, Bennett (2008) DNA repair gets physical: mapping an XPA-binding site on ERCC1. DNA Repair (Amst) 7:819-26
DellaVecchia, Matthew J; Merritt, W Keither; Peng, Ye et al. (2007) NMR analysis of [methyl-13C]methionine UvrB from Bacillus caldotenax reveals UvrB-domain 4 heterodimer formation in solution. J Mol Biol 373:282-95
Meyer, Joel N; Boyd, Windy A; Azzam, Gregory A et al. (2007) Decline of nucleotide excision repair capacity in aging Caenorhabditis elegans. Genome Biol 8:R70
Ruan, Qian; Liu, Tongming; Kolbanovskiy, Alexander et al. (2007) Sequence context- and temperature-dependent nucleotide excision repair of a benzo[a]pyrene diol epoxide-guanine DNA adduct catalyzed by thermophilic UvrABC proteins. Biochemistry 46:7006-15
Karakas, Erkan; Truglio, James J; Croteau, Deborah et al. (2007) Structure of the C-terminal half of UvrC reveals an RNase H endonuclease domain with an Argonaute-like catalytic triad. EMBO J 26:613-22
Kunkel, Thomas A; Van Houten, Bennett (2006) Survival choices. Nat Cell Biol 8:547-9

Showing the most recent 10 out of 30 publications