Journal of Biological Chemistry · 2000 · 182 citations · 43 references
MedicineGeneticsMolecular BiologyGene ExpressionOncogenesTranscriptional RegulationOncogene ActivationTranscription Factor OncogenesUntranslated Regions3' Untranslated Region RegulationBasal Transcription MachineryLuciferase Reporter AssaysNitric OxideNitric Oxide ProductionNitric Oxide Synthase RegulationPost-transcriptional RegulationReporter Gene Construction
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.
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Molecular cloning: A laboratory manual
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