期刊
RADIATION RESEARCH
卷 175, 期 5, 页码 588-598出版社
RADIATION RESEARCH SOC
DOI: 10.1667/RR2084.1
关键词
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资金
- Canadian Cancer Society Research Institute
- Terry Fox Foundation
- Campbell Family Cancer Research Institute
- Canadian Foundation for Innovation
- Ontario Ministry of Health and Long Term Care
- NCIC
- Canadian Cancer Society
We have previously shown that the Ser15-phosphorylated p53 phosphoform, p53(Scr15), can localize at sites of ionizing radiation-induced DNA damage. In this study, we hypothesized that the non-specific DNA binding domain (NSDBD) of the p53 carboxy-terminus (C-terminus) mediates chromatin anchoring at sites of DNA damage to interact with two key mediators of the DNA damage response (DDR): ATM and 53BP1. Exogenous YFP-p53 fusion constructs expressing C-terminus deletion mutants of p53 were transfected into p53-null H1299 cells and tracked by microscopy and biochemistry to determine relative chromatin-binding pre- and postirradiation. We observed that exogenous YFP-p53(wr) and YFP-p53(Delta 367-193) associated with ATM(Ser) (1981) and 53BP1 in the nuclear, chromatin-bound fractions after DNA damage. Of interest, YFP-p53(Delta 1-299) fusion proteins, which lack transcriptional trans-activation and the Ser15-residue, bound to ATM(Ser1981) but not to 53BP1. In support of these data, we used subnuclear UV-microbeam and immunoprecipitation analyses of irradiated normal human fibroblasts (HDFs) that confirmed an interaction between endogenous p53 and ATM or 53BP1. Based on these observations, we propose a model whereby a pre-existing pool of p53 responds immediately to radiation-induced DNA damage using the C-terminus to spatially facilitate protein-protein interactions and the DDR at sites of DNA damage. (C) 2011 by Radiation Research Society
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