IFI16 as a negative regulator in the regulation of p53 and p21(Waf1)

J Biol Chem. 2003 Oct 17;278(42):40899-904. doi: 10.1074/jbc.M308012200. Epub 2003 Aug 18.

Abstract

IFI16 is a member of the HIN-200 family (hematopoietic interferon-inducible nuclear antigens with 200 amino acid repeats) that contains a DNA binding domain, a transcriptional regulatory domain, and DAPIN/PAAD, a protein domain associated with interferon response. It can function as a transcription repressor and directly binds p53. Although the structural and biochemical properties of IFI16 are known, the physiological relevance of these properties in the cellular context is still elusive. Here we report that the inhibition of endogenous IFI16 expression by small interfering RNA (siRNA) induces p21Waf1 mRNA and protein expression through p53 but does not induce pro-apoptotic p53 target genes. This rapid induction of p21 was wild-type p53-dependent and resulted in cell cycle arrest along with a marked reduction of phosphorylated Rb in normally growing cells. We also showed that the repression of IFI16 affects p53 transcriptional activity at the p21 promoter as well as the protein stability of p53 and p21. Our findings identified a new role for IFI16 in modulating p53 function and its target gene regulation in the control of cell cycle regulation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Blotting, Northern
  • Blotting, Western
  • Cell Cycle
  • Cell Line
  • Cell Line, Tumor
  • Chromatin / metabolism
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / metabolism*
  • Cycloheximide / pharmacology
  • Electrophoresis, Polyacrylamide Gel
  • Flow Cytometry
  • Gene Expression Regulation*
  • Humans
  • Molecular Sequence Data
  • Nuclear Proteins*
  • Phosphoproteins*
  • Phosphorylation
  • Precipitin Tests
  • Protein Binding
  • Protein Synthesis Inhibitors / pharmacology
  • Proteins / metabolism*
  • Proteins / physiology*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Retinoblastoma Protein / metabolism
  • Time Factors
  • Transcription, Genetic
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • CDKN1A protein, human
  • Chromatin
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Nuclear Proteins
  • Phosphoproteins
  • Protein Synthesis Inhibitors
  • Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Retinoblastoma Protein
  • Tumor Suppressor Protein p53
  • IFI16 protein, human
  • Cycloheximide