The histone acetyltransferase PCAF regulates p21 transcription through stress-induced acetylation of histone H3

Ian M. Love, Pedja Sekaric, Dingding Shi, Steven R. Grossman, Elliot Androphy

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

The activity of p53 as a tumor suppressor primarily depends on its ability to transactivate specific target genes in response to genotoxic and other potentially mutagenic stresses. Several histone acetyl transferases (HATs), including p300, CBP, PCAF and GCN5 have been implicated in the activation of p53-dependent transcription of the cyclin-dependent kinase (cdk) inhibitor p21 as well as other target genes. Here we show that PCAF, but not CBP or p300, is a critical regulator of p53-dependent p21 expression in response to multiple p53-activating stresses. PCAF was required for the transcriptional activation of p21 in response to exogenous p53 in p53-null cells, Nutlin-3, DNA damaging agents and p14ARF expression, suggesting a broad requirement for PCAF in p53 signaling to p21 after stress. Importantly, cells lacking PCAF failed to undergo cell cycle arrest in response to Nutlin-3 treatment or p14 ARF expression, consistent with a physiologically important role for PCAF in this p53 function. Surprisingly, the role for PCAF in induction of p21 was independent of p53 lysine 320 acetylation, a previously suggested target of PCAF-mediated acetylation. Though p21 promoter occupancy by p53 was not altered by PCAF knockdown, activation of p21 transcription required an intact PCAF HAT domain, and induction of chromatin marks acetyl-H3K9 and acetyl-H3K14 at the p21 promoter by p53 was dependent upon physiologic levels of PCAF. Together, our experiments indicate that PCAF is required for stress-responsive histone 3 acetylation at the p21 promoter, p53-directed transcription of p21 and the resultant growth arrest.

Original languageEnglish
Pages (from-to)2458-2466
Number of pages9
JournalCell Cycle
Volume11
Issue number13
DOIs
StatePublished - Jul 1 2012

Fingerprint

Histone Acetyltransferases
Acetylation
Tumor Suppressor Protein p14ARF
Histones
Transferases
Transcriptional Activation
Cyclin-Dependent Kinase Inhibitor p21
Null Lymphocytes
Cell Cycle Checkpoints
Genes
Lysine
Chromatin
DNA
Growth
Neoplasms
nutlin 3

Keywords

  • ARF
  • DNA damage
  • Histone acetylation
  • p21
  • p53
  • PCAF

ASJC Scopus subject areas

  • Cell Biology
  • Molecular Biology
  • Developmental Biology

Cite this

The histone acetyltransferase PCAF regulates p21 transcription through stress-induced acetylation of histone H3. / Love, Ian M.; Sekaric, Pedja; Shi, Dingding; Grossman, Steven R.; Androphy, Elliot.

In: Cell Cycle, Vol. 11, No. 13, 01.07.2012, p. 2458-2466.

Research output: Contribution to journalArticle

Love, Ian M. ; Sekaric, Pedja ; Shi, Dingding ; Grossman, Steven R. ; Androphy, Elliot. / The histone acetyltransferase PCAF regulates p21 transcription through stress-induced acetylation of histone H3. In: Cell Cycle. 2012 ; Vol. 11, No. 13. pp. 2458-2466.
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AB - The activity of p53 as a tumor suppressor primarily depends on its ability to transactivate specific target genes in response to genotoxic and other potentially mutagenic stresses. Several histone acetyl transferases (HATs), including p300, CBP, PCAF and GCN5 have been implicated in the activation of p53-dependent transcription of the cyclin-dependent kinase (cdk) inhibitor p21 as well as other target genes. Here we show that PCAF, but not CBP or p300, is a critical regulator of p53-dependent p21 expression in response to multiple p53-activating stresses. PCAF was required for the transcriptional activation of p21 in response to exogenous p53 in p53-null cells, Nutlin-3, DNA damaging agents and p14ARF expression, suggesting a broad requirement for PCAF in p53 signaling to p21 after stress. Importantly, cells lacking PCAF failed to undergo cell cycle arrest in response to Nutlin-3 treatment or p14 ARF expression, consistent with a physiologically important role for PCAF in this p53 function. Surprisingly, the role for PCAF in induction of p21 was independent of p53 lysine 320 acetylation, a previously suggested target of PCAF-mediated acetylation. Though p21 promoter occupancy by p53 was not altered by PCAF knockdown, activation of p21 transcription required an intact PCAF HAT domain, and induction of chromatin marks acetyl-H3K9 and acetyl-H3K14 at the p21 promoter by p53 was dependent upon physiologic levels of PCAF. Together, our experiments indicate that PCAF is required for stress-responsive histone 3 acetylation at the p21 promoter, p53-directed transcription of p21 and the resultant growth arrest.

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