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A new transacting factor that modulates hypoxia-induced expression of the erythropoietin gene.
Gupta, M; Mungai, P T; Goldwasser, E.
Afiliação
  • Gupta M; Department of Biochemistry and Molecular Biology, The University of Chicago, IL 60637, USA.
Blood ; 96(2): 491-7, 2000 Jul 15.
Article em En | MEDLINE | ID: mdl-10887110
Hypoxia is a strong stimulus for the transcription of a set of genes, including erythropoietin and vascular endothelial growth factor. Here we report on the cloning, functional significance, and expression of a complementary DNA (cDNA) that is involved in hypoxia-mediated expression of these 2 genes. The full-length cDNA encodes a predicted protein of 806 amino acids that contains a leucine zipper motif. This protein, termed HAF for hypoxia-associated factor, binds to a 17-base pair (bp) region of the erythropoietin promoter, which was shown earlier to participate in hypoxia-induced expression of the erythropoietin gene. In Hep3B cells, clones modified to express HAF antisense RNA showed an attenuated response to hypoxia-mediated induction of both erythropoietin and vascular endothelial growth factor transcription. HAF showed sequence-specific interaction with a DNA element in the 5' untranslated region of VEGF gene. The HAF 2.6-kilobase (kb) messenger RNA (mRNA) is expressed in most adult tissues. The highest expression occurs in fetal liver and the least in adult liver. HAF is the murine homolog of Sart-1, a 125-kd human protein expressed in the nuclei of normal and malignant cells. (Blood. 2000;96:491-497)
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipóxia Celular / Expressão Gênica / Transativadores / Eritropoetina Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Blood Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipóxia Celular / Expressão Gênica / Transativadores / Eritropoetina Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Blood Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos