Hypoxia-inducible nuclear factors bind to an enhancer element located 3' to the human erythropoietin gene.
Author(s) -
Gregg L. Semenza,
M K Nejfelt,
Lamiaa M. Salem,
Stylianos E. Antonarakis
Publication year - 1991
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.88.13.5680
Subject(s) - enhancer , erythropoietin , biology , microbiology and biotechnology , gene expression , gene , hypersensitive site , hypoxia (environmental) , regulation of gene expression , deoxyribonuclease i , regulatory sequence , kidney , genetics , chemistry , oxygen , organic chemistry , base sequence
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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