The causes of genomic rearrangements that lead to cancer are not fully understood. It was recently suggested that a phenomenon called Break-Induced Replication (BIR) is responsible for several cancer-related events, including chromosomal translocations, loss of heterozygosity, and stabilization of chromosomal ends. All three of these events lead to cellular immortalization. BIR, a poorly understood mechanism used by cells to repair chromosomal breaks, is dangerous because it can lead to genetic rearrangements. The long-term goal of this research program is to uncover the mechanisms leading to genetic instability and, in particular, to understand the mechanism of BIR and how it is regulated by living cells to prevent genomic destabilization. The objectives of this particular application include: characterization of gross chromosomal rearrangements (GCRs) associated with repair of double-strand DNA breaks (DSBs), determining the role of BIR information of GCRs, and establishing the role of inverted DNA repeats in promoting chromosomal rearrangements. Yeast Saccharomyces cerevisiae will be used as a model eukaryotic system to study repair of DSBs. Chromosomal rearrangements will be examined by genomic microarray analysis. The physical analysis of molecular intermediates formed by inverted DNA repeats will reveal the role of these DNA motifs in promoting GCRs. The results of our proposed research will provide insights into the mechanisms of chromosomal rearrangements and the role of BIR and specific DNA motifs in promoting GCRs. Relevance. The proposed research is designed to determine the underlying cause of chromosomal aberrations that may be the mechanism for different types of cancer. This study will also identify genetic factors that predispose chromosomes to rearrangements and, therefore, will lead to improved screening procedures aimed to identify individuals who may be """"""""at risk"""""""" for developing cancer due to abnormal patterns of DNA repair. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM074657-01A1
Application #
7073054
Study Section
Special Emphasis Panel (ZRG1-GGG-F (90))
Program Officer
Portnoy, Matthew
Project Start
2006-03-01
Project End
2010-02-28
Budget Start
2006-03-01
Budget End
2010-02-28
Support Year
1
Fiscal Year
2006
Total Cost
$227,250
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Downing, Brandon; Morgan, Rachel; VanHulle, Kelly et al. (2008) Large inverted repeats in the vicinity of a single double-strand break strongly affect repair in yeast diploids lacking Rad51. Mutat Res 645:9-18
Deem, Angela; Barker, Krista; Vanhulle, Kelly et al. (2008) Defective break-induced replication leads to half-crossovers in Saccharomyces cerevisiae. Genetics 179:1845-60
VanHulle, Kelly; Lemoine, Francene J; Narayanan, Vidhya et al. (2007) Inverted DNA repeats channel repair of distant double-strand breaks into chromatid fusions and chromosomal rearrangements. Mol Cell Biol 27:2601-14