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Lookup NU author(s): Dr Ian Logan, Hesta McNeill, Susan Cook, Dr Xiaohong Lu, Professor John LunecORCiD, Professor Craig Robson
Here we define an important role for heat shock factor 1 (HSF1) in the cellular response to genotoxic agents. We demonstrate for the first time that HSF1 can complex with nuclear p53 and that both proteins are co-operatively recruited to p53-responsive genes such as p21. Analysis of natural and synthetic cis elements demonstrates that HSF1 can enhance p53-mediated transcription, whilst depletion of HSF1 reduces the expression of p53-responsive transcripts. We find that HSF1 is required for optimal p21 expression and p53-mediated cell-cycle arrest in response to genotoxins while loss of HSF1 attenuates apoptosis in response to these agents. To explain these novel properties of HSF1 we show that HSF1 can complex with DNA damage kinases ATR and Chk1 to effect p53 phosphorylation in response to DNA damage. Our data reveal HSF1 as a key transcriptional regulator in response to genotoxic compounds widely used in the clinical setting, and suggest that HSF1 will contribute to the efficacy of these agents.
Author(s): Logan IR, McNeill HV, Cook S, Lu X, Meek DW, Fuller-Pace FV, Lunec J, Robson CN
Publication type: Article
Publication status: Published
Journal: Nucleic Acids Research
Year: 2009
Volume: 37
Issue: 9
Pages: 2962-2973
Date deposited: 06/04/2010
ISSN (print): 0305-1048
ISSN (electronic): 1362-4954
Publisher: Oxford University Press
URL: http://dx.doi.org/10.1093/nar/gkp180
DOI: 10.1093/nar/gkp180
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