Aneuploidy is a nearly ubiquitous feature of human cancers. Investigation of the molecular mechanisms of chromosome instability is important for the development of effective strategies for cancer prevention and therapy. The long-term objective of this project is to determine the mechanisms by which genetic and environmental factors affect the fidelity of chromosome segregation. The basic hypotheses of this proposal are that: 1) certain mutations in genes encoding DNA polymerases can cause increased chromosome loss and nondisjunction by disrupting coordination of DNA synthesis and chromosome segregation, and 2) chromosome instability in such mutants can be further increased by exposure to environmental genotoxicants. These hypotheses will be tested by pursuing the following specific aims: (1) develop a novel system for quantitative analysis of chromosome missegregation in yeast that allows direct selection for nondisjunction events, (2) identify mutations in genes encoding DNA polymerases that would lead to increase in spontaneous or environmental genotoxicant-induced chromosome missegregation, and (3) investigate the mechanisms of chromosome segregation defects in mutants identified in aim 2. The effects of UV-irradiation, alkylating agents, oxidative stress and the radiomimetic chemical bleomycin on chromosome stability will be tested. These studies will provide the basis for identification of human genes and environmental factors involved in induction of aneuploidy in human cancer cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Career Transition Award (K22)
Project #
1K22ES011644-01
Application #
6474726
Study Section
Special Emphasis Panel (ZES1-LKB-E (KT))
Program Officer
Shreffler, Carol K
Project Start
2003-09-01
Project End
2006-06-30
Budget Start
2003-09-01
Budget End
2004-06-30
Support Year
1
Fiscal Year
2003
Total Cost
$105,416
Indirect Cost
Name
University of Nebraska Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
168559177
City
Omaha
State
NE
Country
United States
Zip Code
68198
Kochenova, O V; Soshkina, J V; Stepchenkova, E I et al. (2011) Participation of translesion synthesis DNA polymerases in the maintenance of chromosome integrity in yeast Saccharomyces cerevisiae. Biochemistry (Mosc) 76:49-60
Sharma, Neeru M; Kochenova, Olga V; Shcherbakova, Polina V (2011) The non-canonical protein binding site at the monomer-monomer interface of yeast proliferating cell nuclear antigen (PCNA) regulates the Rev1-PCNA interaction and Pol?/Rev1-dependent translesion DNA synthesis. J Biol Chem 286:33557-66
Northam, Matthew R; Robinson, Heather A; Kochenova, Olga V et al. (2010) Participation of DNA polymerase zeta in replication of undamaged DNA in Saccharomyces cerevisiae. Genetics 184:27-42
Northam, Matthew R; Garg, Parie; Baitin, Dmitri M et al. (2006) A novel function of DNA polymerase zeta regulated by PCNA. EMBO J 25:4316-25