| Literature DB >> 15546613 |
Jun Hayakawa1, Shalu Mittal, Yipeng Wang, Kemal S Korkmaz, Eileen Adamson, Christopher English, Masahide Ohmichi, Masahide Omichi, Michael McClelland, Dan Mercola.
Abstract
The NH2-terminal Jun kinases (JNKs) function in diverse roles through phosphorylation and activation of AP-1 components including ATF2 and c-Jun. However, the genes that mediate these processes are poorly understood. A model phenotype characterized by rapid activation of Jun kinase and enhanced DNA repair following cisplatin treatment was examined using chromatin immunoprecipitation with antibodies against ATF2 and c-Jun or their phosphorylated forms and hybridization to promoter arrays. Following genotoxic stress, we identified 269 genes whose promoters are bound upon phosphorylation of ATF2 and c-Jun. Binding did not occur following treatment with transplatin or the JNK inhibitor SP600125 or JNK-specific siRNA. Of 89 known DNA repair genes represented on the array, 23 are specifically activated by cisplatin treatment within 3-6 hr. Thus, the genotoxic stress response occurs at least partly via activation of ATF2 and c-Jun, leading to large-scale coordinate gene expression dominated by genes of DNA repair.Entities:
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Year: 2004 PMID: 15546613 DOI: 10.1016/j.molcel.2004.10.024
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970