Higher order coiling or supercoiling exists in the double-stranded DNA of all organisms as well as some viruses. Negative supercoiling imparts a torsional strain which can produce open or single-stranded regions at specific sites in DNA. These regions may serve as recognition sites for regulatory proteins and enzymes involved in DNA replication, transcription and recombination and may have other functions. The long-term goal of this proposal is to examine the presence, nature and biological significance of single-stranded regions in supercoiled DNA. To achieve this goal, we will (1) evaluate three different single-strand specific endonucleases as probes for open regions in pBR322 DNA by determining the nucleotide sequences cleaved and the effects of environmental conditions and superhelical density on the site specificity, (2) probe the structure of other supercoiled DNAs to test the generality of our findings, and (3) enzymatically delete single-stranded regions to directly test their biological importance in vivo. Knowledge of the relationships between DNA supercoiling, DNA structure and biological function is essential for understanding the regulation and execution of DNA functions in normal and cancer cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM030614-03
Application #
3278412
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1983-03-01
Project End
1986-02-28
Budget Start
1985-03-01
Budget End
1986-02-28
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Minca, Eugen C; Kowalski, David (2011) Replication fork stalling by bulky DNA damage: localization at active origins and checkpoint modulation. Nucleic Acids Res 39:2610-23
Minca, Eugen C; Kowalski, David (2010) Multiple Rad5 activities mediate sister chromatid recombination to bypass DNA damage at stalled replication forks. Mol Cell 38:649-61
Kowalski, David; Pendyala, Lakshmi; Daignan-Fornier, Bertrand et al. (2008) Dysregulation of purine nucleotide biosynthesis pathways modulates cisplatin cytotoxicity in Saccharomyces cerevisiae. Mol Pharmacol 74:1092-100
Huang, Ruea-Yea; Kowalski, David; Minderman, Hans et al. (2007) Small ubiquitin-related modifier pathway is a major determinant of doxorubicin cytotoxicity in Saccharomyces cerevisiae. Cancer Res 67:765-72
Huang, Ruea-Yea; Eddy, Martha; Vujcic, Marija et al. (2005) Genome-wide screen identifies genes whose inactivation confer resistance to cisplatin in Saccharomyces cerevisiae. Cancer Res 65:5890-7
Dziegielewska, Barbara; Kowalski, David; Beerman, Terry A (2004) SV40 DNA replication inhibition by the monofunctional DNA alkylator Et743. Biochemistry 43:14228-37
Huang, Yanlin; Kowalski, David (2004) PATTERNFINDER: combined analysis of DNA regulatory sequences and double-helix stability. BMC Bioinformatics 5:134
Huang, Yanlin; Kowalski, David (2003) WEB-THERMODYN: Sequence analysis software for profiling DNA helical stability. Nucleic Acids Res 31:3819-21
Wang, Y; Vujcic, M; Kowalski, D (2001) DNA replication forks pause at silent origins near the HML locus in budding yeast. Mol Cell Biol 21:4938-48
Wang, Y; Beerman, T A; Kowalski, D (2001) Antitumor drug adozelesin differentially affects active and silent origins of DNA replication in yeast checkpoint kinase mutants. Cancer Res 61:3787-94

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