Complex contribution of the 3′-untranslated region to the expressional regulation of the human inducible nitric-oxide synthase gene -: Involvement of the RNA-binding protein HuR

被引:153
作者
Rodriguez-Pascual, F
Hausding, M
Ihrig-Biedert, I
Furneaux, H
Levy, AP
Förstermann, U
Kleinert, H
机构
[1] Univ Mainz, Dept Pharmacol, D-55101 Mainz, Germany
[2] Mem Sloan Kettering Canc Ctr, Program Mol Pharmacol & Therapeut, New York, NY 10021 USA
[3] Technion Israel Inst Technol, Fac Med, IL-31096 Haifa, Israel
关键词
D O I
10.1074/jbc.M910460199
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytokine stimulation of human DLD-1 cells resulted in a marked expression of nitric-oxide synthase (NOS) II mRNA and protein accompanied by only a moderate increase in transcriptional activity. Also, there was a basal transcription of the NOS II gene, which did not result in measurable NOS II expression. The 3'-untranslated region (3'-UTR) of the NOS II mRNA contains four AUUUA motifs and one AUUUUA motif, known to destabilize the mRNAs of proto-oncogenes, nuclear transcription factors, and cytokines. Luciferase reporter gene constructs containing the NOS II 3'-UTR showed a significantly reduced luciferase activity. The embryonic lethal abnormal vision (ELAV)-like protein HuR was found to bind with high affinity to the adenylate/uridylate-rich elements of the NOS II 3'-UTR. Inhibition of HuR with antisense constructs reduced the cytokine-induced NOS II mRNA, whereas overexpression of HuR potentiated the cytokine-induced NOS II expression. This provides evidence that NOS II expression is regulated at the transcriptional and post-transcriptional level. Binding of HuR to the 3'-UTR of the NOS II mRNA seems to play an essential role in the stabilization of this mRNA.
引用
收藏
页码:26040 / 26049
页数:10
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