Hypoxia-inducible nuclear factors bind to an enhancer element located 3' to the human erythropoietin gene.

نویسندگان

  • G L Semenza
  • M K Nejfelt
  • S M Chi
  • S E Antonarakis
چکیده

Human erythropoietin gene expression in liver and kidney is inducible by anemia or hypoxia. DNase I-hypersensitive sites were identified 3' to the human erythropoietin gene in liver nuclei. A 256-base-pair region of 3' flanking sequence was shown by DNase I protection and electrophoretic mobility-shift assays to bind four or more different nuclear factors, at least two of which are induced by anemia in both liver and kidney, and the region functioned as a hypoxia-inducible enhancer in transient expression assays. These results provide insight into the molecular basis for the regulation of gene expression by a fundamental physiologic stimulus, hypoxia.

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RAPID COMMUNICATION Characterization of Hypoxia-Responsive Enhancer in the Human Erythropoietin Gene Shows Presence of Hypoxia-Inducible 120-Kd Nuclear DNA-Binding Protein in Erythropoietin-Producing and Nonproducing Cells

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Characterization of hypoxia-responsive enhancer in the human erythropoietin gene shows presence of hypoxia-inducible 120-Kd nuclear DNA-binding protein in erythropoietin-producing and nonproducing cells.

Erythropoietin (Epo) production in response to hypoxia or cobalt is primarily mediated by activation of transcription of the Epo gene. Recently an hypoxia responsive enhancer was identified in the 3' flanking region of the mouse and human Epo genes. Using functional analysis in Hep 3B cells we define here the minimal enhancer element as a 29-bp segment starting at the Apa1 site in the 3' flanki...

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 88 13  شماره 

صفحات  -

تاریخ انتشار 1991