A cis-element in the 3'-untranslated region of IkappaB-zeta mRNA governs its stimulus-specific expression

Biochem Biophys Res Commun. 2007 May 11;356(3):785-91. doi: 10.1016/j.bbrc.2007.03.044. Epub 2007 Mar 16.

Abstract

IkappaB-zeta, an essential transcriptional regulator in inflammatory reactions, is induced by microbial substances that stimulate Toll-like receptors and interleukin (IL)-1beta but not by tumor necrosis factor (TNF)-alpha, via specific mRNA stabilization. Here, we attempted to identify a cis-element in IkappaB-zeta mRNA that confers the specific induction. To evaluate the activities of various fragments in the post-transcriptional regulation, we constructed unique reporter plasmids, in which a fragment was inserted downstream of a destabilized luciferase cDNA transcribed by the SV40 early enhancer/promoter. In NIH3T3 cells, a reporter plasmid harboring IkappaB-zeta mRNA exhibited elevated luciferase activity following stimulation with lipopolysaccharide or IL-1beta, but not TNF-alpha, indicating the stimulus-specificity. We found that a 165-nucleotide fragment in the 3'-untranslated region conferred the specific induction. Stimulus-specific induction of IkappaB-zeta was observed by transfection of full-length IkappaB-zeta mRNA, but not of a mRNA without the fragment. Thus, this sequence is essential for the stimulus-specific induction of IkappaB-zeta via a post-transcriptional regulatory mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics*
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Gene Expression Regulation
  • Humans
  • Interleukin-1beta / pharmacology
  • Lipopolysaccharides / pharmacology
  • Luciferases / genetics
  • Mice
  • NIH 3T3 Cells
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • RNA, Messenger / metabolism*
  • Rats
  • Transfection
  • Tumor Necrosis Factor-alpha / pharmacology
  • Up-Regulation

Substances

  • 3' Untranslated Regions
  • Adaptor Proteins, Signal Transducing
  • Interleukin-1beta
  • Lipopolysaccharides
  • Nfkbiz protein, mouse
  • Nuclear Proteins
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Luciferases