Abstract
A human fibroblast cell line with conditional p53 expression displayed a p53-dependent increase in both the protein and mRNA levels of proliferating cell nuclear antigen (PCNA) after exposure to ionizing radiation (IR). The combination of p53 induction and IR cooperated to activate a transiently expressed human PCNA promoter-reporter gene via a p53-responsive element. Chromatin immunoprecipitation assays with antibodies specific for p53 or p300/CREB-binding protein revealed specific p53-dependent enrichment of PCNA promoter sequences in immunoprecipitates of sheared chromatin prepared from irradiated cells. Maximal and specific association of acetylated histone H4 with the PCNA promoter also depended on p53 induction and exposure to IR. These data demonstrate p53 binding to a target site in the PCNA promoter, recruitment of p300/CREB-binding protein, and localized acetylation of histone H4 in an IR-dependent manner. These molecular events are likely to play a role in mediating activation of PCNA gene expression by p53 during the cellular response to DNA damage. The analyses indicate that the combination of p53 induction and IR activate the PCNA gene via mechanisms similar to that of p21/wild-type p53-activated factor but to a lesser extent. This differential regulation of PCNA and p21/wild-type p53-activated factor may establish the proper ratio of the two proteins to coordinate DNA repair with cell cycle arrest.
Highlights
Cellular responses to DNA damage bear upon tumorigenesis and the development of anti-cancer therapies
We showed previously that exposure of a rat fibroblast cell line to ionizing radiation (IR) increased endogenous proliferating cell nuclear antigen (PCNA) mRNA levels and altered p53 binding to human PCNA promoter sequences in vitro [36]
To address mechanisms of PCNA promoter regulation in native chromatin by p53 and/or IR, we describe here results obtained with a human fibroblast cell line, TR9-7 cells, in which expression of wild-type p53 could be induced by withdrawal of tetracycline [41]
Summary
Cellular responses to DNA damage bear upon tumorigenesis and the development of anti-cancer therapies. The increase of both p21/WAF1 and PCNA protein levels by p53 induction and IR is consistent with their physiological roles in the cellular response to DNA damage, participation in cell cycle arrest, and DNA repair.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.