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      Hypoxic stabilization of vascular endothelial growth factor mRNA by the RNA-binding protein HuR.

      The Journal of Biological Chemistry
      Anoxia, metabolism, Antigens, Surface, Base Sequence, Cells, Cultured, DNA, Antisense, Endothelial Growth Factors, biosynthesis, genetics, Gene Expression Regulation, Half-Life, Hu Paraneoplastic Encephalomyelitis Antigens, Lymphokines, Molecular Sequence Data, Protein Binding, RNA, Messenger, RNA-Binding Proteins, Regulatory Sequences, Nucleic Acid, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factors

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          Abstract

          Vascular endothelial growth factor (VEGF) is a potent angiogenic factor whose expression is dramatically induced by hypoxia due in large part to an increase in the stability of its mRNA. Here we show that HuR binds with high affinity and specificity to the element that regulates VEGF mRNA stability by hypoxia. Inhibition of HuR expression abrogates the hypoxia-mediated increase in VEGF mRNA stability. Overexpression of HuR increases the stability of VEGF mRNA. However, this only occurs efficiently in hypoxic cells. We further show that the stabilization of VEGF mRNA can be recapitulated in vitro. Using an S-100 extract, we show that the addition of recombinant HuR stabilizes VEGF mRNA markedly. These data support the critical role of HuR in mediating the hypoxic stabilization of VEGF mRNA by hypoxia.

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