Acetylation of p53 at lysine 373/382 by the histone deacetylase inhibitor depsipeptide induces expression of p21(Waf1/Cip1).
Generally, histone deacetylase (HDAC) inhibitor-induced p21(Waf1/Cip1) expression is thought to be p53 independent. Here we found that an inhibitor of HDAC, depsipeptide (FR901228), but not trichostatin A (TSA), induces p21(Waf1/Cip1) expression through both p53 and Sp1/Sp3 pathways in A549 cells (which retain wild-type p53). This is demonstrated by measuring relative ... luciferase activities of p21 promoter constructs with p53 or Sp1 binding site mutagenesis and was further confirmed by transfection of wild-type p53 into H1299 cells (p53 null). That p53 was acetylated after depsipeptide treatment was tested by sequential immunoprecipitation/Western immunoblot analysis with anti-acetylated lysines and anti-p53 antibodies. The acetylated p53 has a longer half-life due to a significant decrease in p53 ubiquitination. Further study using site-specific antiacetyllysine antibodies and transfection of mutated p53 vectors (K319/K320/K321R mutated and K373R/K382R mutations) into H1299 cells revealed that depsipeptide specifically induces p53 acetylation at K373/K382, but not at K320. As assayed by coimmunoprecipitation, the K373/K382 acetylation is accompanied by a recruitment of p300, but neither CREB-binding protein (CBP) nor p300/CBP-associated factor (PCAF), to the p53 C terminus. Furthermore, activity associated with the binding of the acetylated p53 at K373/K382 to the p21 promoter as well as p21(Waf1/Cip1) expression is significantly increased after depsipeptide treatment, as tested by chromatin immunoprecipitations and Western blotting, respectively. In addition, p53 acetylation at K373/K382 is confirmed to be required for recruitment of p300 to the p21 promoter, and the depsipeptide-induced p53 acetylation at K373/K382 is unlikely to be dependent on p53 phosphorylation at Ser15, Ser20, and Ser392 sites. Our data suggest that p53 acetylation at K373/K382 plays an important role in depsipeptide-induced p21(Waf1/Cip1) expression.
Mesh Terms:
Acetylation, Cyclin-Dependent Kinase Inhibitor p21, Depsipeptides, Dose-Response Relationship, Drug, Gene Expression Regulation, Half-Life, Histone Deacetylase Inhibitors, Humans, Lysine, Phosphorylation, Promoter Regions, Genetic, Protein Processing, Post-Translational, RNA, Messenger, Serine, Sp1 Transcription Factor, Time Factors, Tumor Cells, Cultured, Tumor Suppressor Protein p53, p300-CBP Transcription Factors
Acetylation, Cyclin-Dependent Kinase Inhibitor p21, Depsipeptides, Dose-Response Relationship, Drug, Gene Expression Regulation, Half-Life, Histone Deacetylase Inhibitors, Humans, Lysine, Phosphorylation, Promoter Regions, Genetic, Protein Processing, Post-Translational, RNA, Messenger, Serine, Sp1 Transcription Factor, Time Factors, Tumor Cells, Cultured, Tumor Suppressor Protein p53, p300-CBP Transcription Factors
Mol. Cell. Biol.
Date: Apr. 01, 2006
PubMed ID: 16537920
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