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pubmed-article:18499678pubmed:abstractTextProtein Arg methyltransferases function as coactivators of the tumor suppressor p53 to regulate gene expression. Peptidylarginine deiminase 4 (PAD4/PADI4) counteracts the functions of protein Arg methyltransferases in gene regulation by deimination and demethylimination. Here we show that the expression of a tumor suppressor gene, OKL38, is activated by the inhibition of PAD4 or the activation of p53 following DNA damage. Chromatin immunoprecipitation assays showed a dynamic change of p53 and PAD4 occupancy and histone Arg modifications at the OKL38 promoter during DNA damage, suggesting a direct role of PAD4 and p53 in the expression of OKL38. Furthermore, we found that OKL38 induces apoptosis through localization to mitochondria and induction of cytochrome c release. Together, our studies identify OKL38 as a novel p53 target gene that is regulated by PAD4 and plays a role in apoptosis.lld:pubmed
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pubmed-article:18499678pubmed:authorpubmed-author:WangYanmingYlld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:ThompsonPaul...lld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:PughB...lld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:YaoHongjieHlld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:VentersBryan...lld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:ZhengSutingSlld:pubmed
pubmed-article:18499678pubmed:authorpubmed-author:LiPingxinPlld:pubmed
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