Rodriguez-Pascual F, Hausding M, Ihrig-Biedert I, Furneaux H, Levy A P, Förstermann U, Kleinert H
Department of Pharmacology, Johannes Gutenberg University, Obere Zahlbacher Strasse 67, D-55101 Mainz, Germany.
J Biol Chem. 2000 Aug 25;275(34):26040-9. doi: 10.1074/jbc.M910460199.
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.
细胞因子刺激人DLD - 1细胞导致一氧化氮合酶(NOS)II mRNA和蛋白的显著表达,同时转录活性仅适度增加。此外,NOS II基因存在基础转录,但未导致可测量的NOS II表达。NOS II mRNA的3' - 非翻译区(3' - UTR)包含四个AUUUA基序和一个AUUUUA基序,已知这些基序会使原癌基因、核转录因子和细胞因子的mRNA不稳定。含有NOS II 3' - UTR的荧光素酶报告基因构建体显示荧光素酶活性显著降低。发现胚胎致死异常视觉(ELAV)样蛋白HuR与NOS II 3' - UTR富含腺苷酸/尿苷酸的元件具有高亲和力结合。用反义构建体抑制HuR可降低细胞因子诱导的NOS II mRNA,而HuR的过表达增强了细胞因子诱导的NOS II表达。这提供了证据表明NOS II表达在转录和转录后水平受到调控。HuR与NOS II mRNA的3' - UTR结合似乎在该mRNA的稳定性中起重要作用。