The proximal region of the 3′-untranslated region of cyclooxygenase-2 is recognized by a multimeric protein complex containing HuR, TIA-1, TIAR, and the heterogeneous nuclear ribonucleoprotein U
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Cok, SJ
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机构:Washington Univ, Sch Med, Wohl Clin, Dept Med, St Louis, MO 63110 USA
Cok, SJ
Acton, SJ
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机构:Washington Univ, Sch Med, Wohl Clin, Dept Med, St Louis, MO 63110 USA
Acton, SJ
Morrison, AR
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机构:Washington Univ, Sch Med, Wohl Clin, Dept Med, St Louis, MO 63110 USA
Morrison, AR
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[1] Washington Univ, Sch Med, Wohl Clin, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Mol Biol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Pharmacol, St Louis, MO 63110 USA
Cyclooxygenase-2 (COX-2) is an early response gene induced in renal mesangial cells by interleukin-1beta (IL-1beta). The 3'-untranslated region (3'-UTR) of COX-2 mRNA plays an important role in IL-1beta induction by regulating message stability and translational efficiency. The first 60 nucleotides of the 3'-UTR of COX-2 are highly conserved and contain multiple copies of the regulatory sequence AUUUA. Introduction of the 60-nucleotide sequence into the 3'-UTR of a heterologous reporter gene resulted in a 70% decrease in reporter gene expression. Electrophoretic mobility shift assays (EMSAs) demonstrated that mesangial cell nuclear fractions contain a multimeric protein complex that bound this region of COX-2 mRNA in a sequence-specific manner. We identified four members of the protein-RNA complex as HuR, TIA-1, TIAR, and the heterogeneous nuclear ribonucleoprotein U (hnRNP U). Treatment of mesangial cells with IL-1beta caused an increase in cytosolic HuR, which was accompanied by an increase in COX-2 mRNA that co-immunoprecipitated with cytosolic HuR. Therefore, we propose that HuR binds to the proximal region of the 3'-UTR of COX-2 following stimulation by IL-1beta and increases the expression of COX-2 mRNA by facilitating its transport out of the nucleus.
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Dean, JLE
Wait, R
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Wait, R
Mahtani, KR
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Mahtani, KR
Sully, G
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Sully, G
Clark, AR
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Clark, AR
Saklatvala, J
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Dean, JLE
Wait, R
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Wait, R
Mahtani, KR
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Mahtani, KR
Sully, G
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Sully, G
Clark, AR
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
Clark, AR
Saklatvala, J
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Imperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, EnglandImperial Coll Sch Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England