Function of polo-like kinase 3 in NF-kappaB-mediated proapoptotic response

J Biol Chem. 2005 Apr 29;280(17):16843-50. doi: 10.1074/jbc.M410119200. Epub 2005 Jan 25.

Abstract

RelA, the p65 subunit of NF-kappaB transcription factors, plays a key role in regulation of antiapoptotic and proapoptotic responses. However, the downstream target genes regulated by RelA-NF-kappaB in the initiation of proapoptotic signaling were not identified. We previously showed that RelA-NF-kappaB functioned as a proapoptotic factor by activating the p53-signaling pathway in response to doxycycline-induced superoxide. In the present study, we demonstrate that the ability of doxycycline/superoxide to induce expression of polo-like kinase 3 (Plk3) depends on NF-kappaB activity. We identified a kappaB binding site in the promoter of Plk3, and this kappaB site is directly involved in its induction by the RelA-NF-kappaB complex. Plk3 formed a complex with p53 and was involved in the phosphorylation of p53 on Ser-20 in response to superoxide. Inhibition of Plk3 expression by Plk3 small interfering RNA suppressed the doxycycline/superoxide-mediated apoptosis. Overexpression of wild-type Plk3 in HCT116 p53+/+ cells induced rapid apoptosis, whereas overexpression of wild-type Plk3 in HCT116 p53-/- cells and the kinase-defective mutant Plk3(K91R) in p53+/+ cells induced delayed onset of apoptosis. Furthermore, mutagenesis of Plk3 showed that the N-terminal domain (amino acids 1-26) is essential for the induction of delay onset of apoptosis. These data show that Plk3 is a RelA-NF-kappaB-regulated gene that induces apoptosis in both p53-dependent and -independent signaling pathways, suggesting a possible mechanism for RelA-NF-kappaB-regulated proapoptotic responses.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apoptosis*
  • Binding Sites
  • Blotting, Northern
  • Blotting, Western
  • Cell Cycle Proteins / metabolism
  • Cell Line
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Cyclin-Dependent Kinase Inhibitor p21
  • DNA Fragmentation
  • Doxycycline / pharmacology
  • Gene Expression Regulation*
  • Genes, p53
  • Humans
  • I-kappa B Proteins / metabolism
  • Immunohistochemistry
  • Luciferases / metabolism
  • Microscopy, Fluorescence
  • Models, Biological
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism*
  • NF-kappa B / physiology
  • Phosphorylation
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Serine-Threonine Kinases / physiology*
  • Protein Structure, Tertiary
  • RNA, Small Interfering / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Serine / chemistry
  • Signal Transduction
  • Time Factors
  • Transcription Factor RelA
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism
  • Tumor Suppressor Proteins

Substances

  • CDKN1A protein, human
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • I-kappa B Proteins
  • NF-kappa B
  • NFKBIA protein, human
  • RNA, Small Interfering
  • Transcription Factor RelA
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • NF-KappaB Inhibitor alpha
  • Serine
  • Luciferases
  • PLK3 protein, human
  • Protein Serine-Threonine Kinases
  • Doxycycline