The long term objective of the project is to identify the mechanism by which radiation induces G1 arrest in cells. The key step in the induction of G1 arrest is the transcriptional activation of the p21 gene (also called WAF-1/Cip-1). The hypothesis to be tested is that radiation activation of the p21 gene occurs through the binding of appropriately phosphorylated p53 to specific sequences in the p21 promoter.
Three specific aims will be undertaken. (1) The activation of p53 following the irradiation of cells may require alterations in the phosphorylation of the p53 protein. The serine phosphorylation sites in p53 will be individually point mutated to alanine to abolish radiation dependent phosphorylation. We will determine how the loss of these p53 phosphorylation sites affects the important functional properties of the p53 protein, including DNA binding, protein stability, phosphorylation status and transcriptional activation of the p21 gene. (2) The most important target of radiation activated p53 is the p21 gene. The p21 protein is able to inhibit cdk2 kinase, a kinase whose activity is required for entry into S-phase. The hypothesis that radiation activation of the p21 gene requires the binding of appropriately phosphorylated p53 will be tested. A series of deletions in the control sequences of the p21 promoter (including p53 binding sites) will be constructed. These will be used to determine which regions of the p21 promoter are required for radiation and DNA damage stimulated transcription of the p21 gene. The binding site for factors which regulate p21 transcription, including p53, will be identified. (3) The biological properties of p53 proteins containing serine mutations will be determined by measuring their ability to induce G1. The biochemical properties of the p53 serine mutations determined in (1) and (2) will then be related to their ability to induce G1 arrest. An understanding of how cells respond to DNA damage, especially mechanisms which may help the cell survive radiation, such as the p53 response, may allow new therapeutic approaches, including the design of novel therapeutic compounds, to be applied to radiation therapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA064585-01A1
Application #
2107159
Study Section
Radiation Study Section (RAD)
Project Start
1995-04-01
Project End
1998-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02215
Dhar, Surbhi; Gursoy-Yuzugullu, Ozge; Parasuram, Ramya et al. (2017) The tale of a tail: histone H4 acetylation and the repair of DNA breaks. Philos Trans R Soc Lond B Biol Sci 372:
Price, Brendan D (2017) KDM5A demethylase: Erasing histone modifications to promote repair of DNA breaks. J Cell Biol 216:1871-1873
Ströbel, Thomas; Madlener, Sibylle; Tuna, Serkan et al. (2017) Ape1 guides DNA repair pathway choice that is associated with drug tolerance in glioblastoma. Sci Rep 7:9674
Gursoy-Yuzugullu, Ozge; Carman, Chelsea; Serafim, Rodolfo Bortolozo et al. (2017) Epigenetic therapy with inhibitors of histone methylation suppresses DNA damage signaling and increases glioma cell radiosensitivity. Oncotarget 8:24518-24532
Day, Tovah A; Layer, Jacob V; Cleary, J Patrick et al. (2017) PARP3 is a promoter of chromosomal rearrangements and limits G4 DNA. Nat Commun 8:15110
Gursoy-Yuzugullu, Ozge; Carman, Chelsea; Price, Brendan D (2017) Spatially restricted loading of BRD2 at DNA double-strand breaks protects H4 acetylation domains and promotes DNA repair. Sci Rep 7:12921
Gursoy-Yuzugullu, Ozge; House, Nealia; Price, Brendan D (2016) Patching Broken DNA: Nucleosome Dynamics and the Repair of DNA Breaks. J Mol Biol 428:1846-60
Gursoy-Yuzugullu, Ozge; Ayrapetov, Marina K; Price, Brendan D (2015) Histone chaperone Anp32e removes H2A.Z from DNA double-strand breaks and promotes nucleosome reorganization and DNA repair. Proc Natl Acad Sci U S A 112:7507-12
Du, Fengxia; Zhang, Minjie; Li, Xiaohua et al. (2014) Dimer monomer transition and dimer re-formation play important role for ATM cellular function during DNA repair. Biochem Biophys Res Commun 452:1034-9
Ayrapetov, Marina K; Gursoy-Yuzugullu, Ozge; Xu, Chang et al. (2014) DNA double-strand breaks promote methylation of histone H3 on lysine 9 and transient formation of repressive chromatin. Proc Natl Acad Sci U S A 111:9169-74

Showing the most recent 10 out of 38 publications