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      General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Base Sequence, Binding Sites, CHO Cells, Carcinoma, Hepatocellular, Cell Hypoxia, Cell Nucleus, metabolism, radiation effects, Chloramphenicol O-Acetyltransferase, genetics, Cricetinae, DNA-Binding Proteins, isolation & purification, Enhancer Elements, Genetic, Erythropoietin, biosynthesis, Gene Expression Regulation, Neoplastic, HeLa Cells, Humans, Hypoxia-Inducible Factor 1, Hypoxia-Inducible Factor 1, alpha Subunit, Liver Neoplasms, Macromolecular Substances, Molecular Sequence Data, Nuclear Proteins, Oligonucleotide Probes, Recombinant Fusion Proteins, Transcription Factors, Transcription, Genetic, Transfection, Tumor Cells, Cultured, Ultraviolet Rays, beta-Galactosidase

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          Abstract

          Transcription of the human erythropoietin (EPO) gene is activated in Hep3B cells exposed to hypoxia. Hypoxia-inducible factor 1 (HIF-1) is a nuclear factor whose DNA binding activity is induced by hypoxia in Hep3B cells, and HIF-1 binds at a site in the EPO gene enhancer that is required for hypoxic activation of transcription. In this paper, we demonstrate that HIF-1 DNA binding activity is also induced by hypoxia in a variety of mammalian cell lines in which the EPO gene is not transcribed. The composition of the HIF-1 DNA binding complex and its isolated DNA binding subunit and the mechanism of HIF-1 activation appear to be similar or identical in EPO-producing and non-EPO-producing cells. Transcription of reporter genes containing the EPO gene enhancer is induced by hypoxia in non-EPO-producing cells and mutations that eliminate HIF-1 binding eliminate inducibility. These results provide evidence that HIF-1 and its recognition sequence are common components of a general mammalian cellular response to hypoxia.

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