Transcriptional induction of protein kinase C delta by p53 tumor suppressor in the apoptotic response to DNA damage

Nurmaa Dashzeveg, Satomi Yogosawa, Kiyotsugu Yoshida*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Genetic alterations and aberrant gene expression trigger malignant tumors. Tumor suppressor p53 is the most altered gene in human cancers. p53 induces apoptosis by promoting pro-apoptotic genes in response to DNA damage. Protein kinase C delta (PKCδ) also induces apoptosis via various mechanisms including modification of p53. The PKCδ-dependent apoptotic mechanism has been extensively studied; however, the transcriptional regulation of PKCδ remains obscure. The current study demonstrates the transcriptional regulation of PKCδ by p53 upon genotoxic stress. The p53-binding site in the promoter region of PKCδ was detected by the ChIP-sequencing assay. Notably, the expression of PKCδ was increased upon DNA damage, which is required for the stabilization of p53. More importantly, targeting single guide RNA-driven dead Cas9 to the p53-binding site of PKCδ disturbed p53-promoted PKCδ expression and suppressed apoptosis following DNA damage. Thus, our findings suggest that the transcriptional regulation of PKCδ is controlled by p53 in a positive feedback mechanism to induce apoptosis in response to DNA damage.

Original languageEnglish (US)
Pages (from-to)167-174
Number of pages8
JournalCancer Letters
Volume374
Issue number1
DOIs
StatePublished - Apr 28 2016

Keywords

  • Apoptosis
  • CRISPRi
  • DNA damage
  • P53
  • PKCδ
  • Tumor suppressor

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Transcriptional induction of protein kinase C delta by p53 tumor suppressor in the apoptotic response to DNA damage'. Together they form a unique fingerprint.

Cite this