TY - JOUR
T1 - A cis-element in the 3′-untranslated region of IκB-ζ mRNA governs its stimulus-specific expression
AU - Watanabe, Satoshi
AU - Takeshige, Koichiro
AU - Muta, Tatsushi
N1 - Funding Information:
This work was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan (to T.M. and K.T.), and Grants from the Naito Foundation (to T.M.), the Mochida Memorial Foundation for Medical and Pharmaceutical Research (to T.M.), the Kaibara Foundation (to T.M.), and the Japan Foundation of Applied Enzymology (to T.M.).
PY - 2007/5/11
Y1 - 2007/5/11
N2 - IκB-ζ, an essential transcriptional regulator in inflammatory reactions, is induced by microbial substances that stimulate Toll-like receptors and interleukin (IL)-1β but not by tumor necrosis factor (TNF)-α, via specific mRNA stabilization. Here, we attempted to identify a cis-element in IκB-ζ 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 IκB-ζ mRNA exhibited elevated luciferase activity following stimulation with lipopolysaccharide or IL-1β, but not TNF-α, indicating the stimulus-specificity. We found that a 165-nucleotide fragment in the 3′-untranslated region conferred the specific induction. Stimulus-specific induction of IκB-ζ was observed by transfection of full-length IκB-ζ mRNA, but not of a mRNA without the fragment. Thus, this sequence is essential for the stimulus-specific induction of IκB-ζ via a post-transcriptional regulatory mechanism.
AB - IκB-ζ, an essential transcriptional regulator in inflammatory reactions, is induced by microbial substances that stimulate Toll-like receptors and interleukin (IL)-1β but not by tumor necrosis factor (TNF)-α, via specific mRNA stabilization. Here, we attempted to identify a cis-element in IκB-ζ 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 IκB-ζ mRNA exhibited elevated luciferase activity following stimulation with lipopolysaccharide or IL-1β, but not TNF-α, indicating the stimulus-specificity. We found that a 165-nucleotide fragment in the 3′-untranslated region conferred the specific induction. Stimulus-specific induction of IκB-ζ was observed by transfection of full-length IκB-ζ mRNA, but not of a mRNA without the fragment. Thus, this sequence is essential for the stimulus-specific induction of IκB-ζ via a post-transcriptional regulatory mechanism.
KW - Induction
KW - Innate immunity
KW - Interleukin-1β
KW - IκB-ζ
KW - MyD88
KW - NF-κB
KW - Post-transcriptional regulation
KW - TLR
KW - mRNA stability
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U2 - 10.1016/j.bbrc.2007.03.044
DO - 10.1016/j.bbrc.2007.03.044
M3 - Article
C2 - 17382899
AN - SCOPUS:33947699876
VL - 356
SP - 785
EP - 791
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 3
ER -