DNA helicases are ubiquitous and vast in number, serving important roles in various facets of chromosome metabolism, including transcription, DNA replication, and DNA repair. We have been interested in a unique class of helicases called the RecQ family, with five distinct members in humans. Genetic defects in three of these helicases, viz., BLM, RTS, and WRN, give rise to human syndromes associated with cancer predisposition. Importantly, genetic ablation of RecQ5 also engenders cancer susceptibility in mice. Thus, the RecQ helicases are clearly important for genome maintenance and cancer avoidance. The BLM helicase, mutations in which being the cause of the radiation-sensitive and cancer-prone disorder Bloom's syndrome, functions in two critical stages of homologous recombination (HR)- mediated chromosome damage repair, namely, in the resection of DNA double-strand breaks and the dissolution of the double Holliday Junction, a late HR intermediate. Defects in BLM and its partner proteins thus lead to impaired initiation of homologous repair, frequent sister chromatid exchanges, and chromosome aberrations. Even though RECQ5 has not yet been associated with a human disease, its ablation in mice results in cancer susceptibility. RECQ5-deficient cells exhibit DNA damage sensitivity, elevated sister chromatid exchanges and HR events, and are prone to chromosomal rearrangements upon genotoxic stress. RECQ5 physically interacts with the RAD51 recombinase and displaces RAD51 from DNA. These results implicate RECQ5 as a tumor suppressor that acts by preventing inappropriate HR events via the disruption of RAD51-DNA nucleoprotein filaments. In this renewal project, we will strive to delineate the multi-faceted role of BLM in HR repair and regulation, and to also define the mechanism underlying the novel role of RECQ5 as an anti-recombinase.

Public Health Relevance

Failure to properly repair damaged chromosomes or regulate the repair process compromises the integrity of the genome and can lead to cancer formation. The proposed studies will define the role of two human RecQ helicases and their partner proteins in the homologous recombinational repair of chromosomes that harbor radiation-induced DNA double-strand breaks and other deleterious lesions. The results will make a major contribution toward delineating the mechanism of DNA homology- directed chromosome damage repair and its regulation in human cells, and have strong relevance to radiation and cancer biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
2R01ES015632-06A1
Application #
8433810
Study Section
Radiation Therapeutics and Biology Study Section (RTB)
Program Officer
Reinlib, Leslie J
Project Start
2007-04-16
Project End
2017-10-31
Budget Start
2012-12-01
Budget End
2013-10-31
Support Year
6
Fiscal Year
2013
Total Cost
$416,288
Indirect Cost
$165,512
Name
Yale University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Crickard, J Brooks; Kaniecki, Kyle; Kwon, Youngho et al. (2018) Meiosis-specific recombinase Dmc1 is a potent inhibitor of the Srs2 antirecombinase. Proc Natl Acad Sci U S A 115:E10041-E10048
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De Tullio, Luisina; Kaniecki, Kyle; Kwon, Youngho et al. (2017) Yeast Srs2 Helicase Promotes Redistribution of Single-Stranded DNA-Bound RPA and Rad52 in Homologous Recombination Regulation. Cell Rep 21:570-577
Buzovetsky, Olga; Kwon, Youngho; Pham, Nhung Tuyet et al. (2017) Role of the Pif1-PCNA Complex in Pol ?-Dependent Strand Displacement DNA Synthesis and Break-Induced Replication. Cell Rep 21:1707-1714
Kumar, S; Peng, X; Daley, J et al. (2017) Inhibition of DNA2 nuclease as a therapeutic strategy targeting replication stress in cancer cells. Oncogenesis 6:e319
Wang, Weibin; Daley, James M; Kwon, Youngho et al. (2017) Plasticity of the Mre11-Rad50-Xrs2-Sae2 nuclease ensemble in the processing of DNA-bound obstacles. Genes Dev 31:2331-2336
Chen, Xuefeng; Niu, Hengyao; Yu, Yang et al. (2016) Enrichment of Cdk1-cyclins at DNA double-strand breaks stimulates Fun30 phosphorylation and DNA end resection. Nucleic Acids Res 44:2742-53

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