Functional role of NF-IL6beta and its sumoylation and acetylation modifications in promoter activation of cyclooxygenase 2 gene

Nucleic Acids Res. 2006 Jan 5;34(1):217-31. doi: 10.1093/nar/gkj422. Print 2006.

Abstract

NF-IL6beta regulates gene expression and plays function roles in many tissues. The EGF-regulated cyclooxygenase-2 (cox-2) expression is mediated through p38(MAPK) signaling pathway and positively correlates with NF-IL6beta expression in A431 cells. NF-IL6beta coordinated with c-Jun on cox-2 transcriptional activation by reporter and small interfering RNA assays. NF-IL6beta could directly bind to CCAAT/enhancer-binding protein (C/EBP) and cyclic AMP-response element (CRE) sites of the cox-2 promoter by in vitro-DNA binding assay. The C/EBP site was important for basal and, to a lesser extent, for EGF-regulated cox-2 transcription, while the CRE site was a more specific response to EGF inducibility of cox-2 gene. SUMO1 expression attenuated EGF- and NF-IL6beta-induced cox-2 promoter activities. NF-IL6beta was found to be sumoylated by in vivo- and in vitro-sumoylation assays, and the SUMO1-NF-IL6beta (suNF-IL6beta) lost its ability to interact with p300 in in vitro-binding assay. NF-IL6beta was also acetylated by p300, and acetylation of NF-IL6beta enhanced the cox-2 promoter activity stimulated by NF-IL6beta itself. In vivo-DNA binding assay demonstrated that EGF stimulated the recruitment of p300 and NF-IL6beta to the cox-2 promoter, yet promoted the dissociation of SUMO1-modificated proteins from the promoter. These results indicated that NF-IL6beta plays a pivotal role in the regulation of basal and EGF-induced cox-2 transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Binding Sites
  • CCAAT-Enhancer-Binding Protein-delta / metabolism*
  • CCAAT-Enhancer-Binding Protein-delta / physiology
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Cell Cycle Proteins / antagonists & inhibitors
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Cyclic AMP / metabolism
  • Cyclooxygenase 2 / biosynthesis
  • Cyclooxygenase 2 / genetics*
  • Epidermal Growth Factor / antagonists & inhibitors
  • Gene Expression Regulation, Enzymologic*
  • Histone Acetyltransferases / antagonists & inhibitors
  • Histone Acetyltransferases / metabolism
  • Imidazoles / pharmacology
  • Promoter Regions, Genetic
  • Protein Kinase Inhibitors / pharmacology
  • Protein Processing, Post-Translational*
  • Pyridines / pharmacology
  • Response Elements
  • SUMO-1 Protein / metabolism
  • Transcription Factors / antagonists & inhibitors
  • Transcription Factors / metabolism
  • Transcriptional Activation*
  • p300-CBP Transcription Factors
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors

Substances

  • CCAAT-Enhancer-Binding Proteins
  • CEBPD protein, human
  • Cell Cycle Proteins
  • Imidazoles
  • Protein Kinase Inhibitors
  • Pyridines
  • SUMO-1 Protein
  • Transcription Factors
  • CCAAT-Enhancer-Binding Protein-delta
  • Epidermal Growth Factor
  • Cyclic AMP
  • Cyclooxygenase 2
  • Histone Acetyltransferases
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580