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The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha.

The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Research Abstract Details 

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  • The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Abstract Text:

    cheng-jun huCheng-Jun Hu,aneesa sataurAneesa Sataur,liyi wangLiyi Wang,hongqing chenHongqing Chen,m celeste simonM Celeste Simon,cheng-jun huCheng-Jun Hu,aneesa sataurAneesa Sataur,liyi wangLiyi Wang,hongqing chenHongqing Chen,m celeste simonM Celeste Simon,

    The basic helix-loop-helix-Per-ARNT-Sim-proteins hypoxia-inducible factor (HIF)-1alpha and HIF-2alpha are the principal regulators of the hypoxic transcriptional response. Although highly related, they can activate distinct target genes. In this study, the protein domain and molecular mechanism important for HIF target gene specificity are determined. We demonstrate that although HIF-2alpha is unable to activate multiple endogenous HIF-1alpha-specific target genes (e.g., glycolytic enzymes), HIF-2alpha still binds to their promoters in vivo and activates reporter genes derived from such targets. In addition, comparative analysis of the N-terminal DNA binding and dimerization domains of HIF-1alpha and HIF-2alpha does not reveal any significant differences between the two proteins. Importantly, replacement of the N-terminal transactivation domain (N-TAD) (but not the DNA binding domain, dimerization domain, or C-terminal transactivation domain [C-TAD]) of HIF-2alpha with the analogous region of HIF-1alpha is sufficient to convert HIF-2alpha into a protein with HIF-1alpha functional specificity. Nevertheless, both the N-TAD and C-TAD are important for optimal HIF transcriptional activity. Additional experiments indicate that the ETS transcription factor ELK is required for HIF-2alpha to activate specific target genes such as Cited-2, EPO, and PAI-1. These results demonstrate that the HIF-alpha TADs, particularly the N-TADs, confer HIF target gene specificity, by interacting with additional transcriptional cofactors.

    The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Publishing Authors By Initials

    cj huCJ Hu,a sataurA Sataur,l wangL Wang,h chenH Chen,mc simonMC Simon,cj huCJ Hu,a sataurA Sataur,l wangL Wang,h chenH Chen,mc simonMC Simon,

    For similar abstracts research abstracts see: abstracts research

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    The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Molecular biology of the cell

    VOLUME: 18

    Page Numbers: 4528-42

    Journal Abbreviation: Mol. Biol. Cell

    ISSN: 1059-1524

    DAY: 5

    MONTH: 09

    YEAR: 2007

    The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Information

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    LANGUAGE: eng

    NlmUniqueID: 9201390

    The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha. Keywords Mesh Terms:

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    Grant and Affiliation Information for The N-terminal transactivation domain confers target gene specificity of hypoxia-inducible factors HIF-1alpha and HIF-2alpha.

    AFFILIATION: Abramson Family Cancer Research Institute,University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States PHS

    GRANT: 66130

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    MEDLINETA: Mol Biol Cell

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