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New insights into the regulation of cytochrome P450 2C9 gene expression: the role of the transcription factor GATA-4

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F10%3A10080502" target="_blank" >RIV/00179906:_____/10:10080502 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    New insights into the regulation of cytochrome P450 2C9 gene expression: the role of the transcription factor GATA-4

  • Original language description

    CYP2C9 is an important drug-metabolizing enzyme. However, its endogenous regulation is largely unknown. We examined the role of GATA transcription factors in the gene expression of CYP2C9. We investigated four putative GATA binding sites within the first200bp of CYP2C9 promoter at the positions I: -173/-170, II: -167/-164, III: -118/-115, and IV: -106/-103. Luciferase activity driven by a wild-type CYP2C9 promoter construct was strongly up-regulated in Huh-7 cells co-transfected with GATA-2 and GATA-4,whereas mutations introduced into GATA binding site III or I and II reduced this induction significantly. Electrophoretic mobility shift assays revealed specific binding of GATA-4 and GATA-6 to the oligonucleotides containing GATA binding sites I and II. Furthermore, the association of GATA-4 with CYP2C9 promoter was confirmed by chromatin immunoprecipitation in HepG2 cells. These data strongly suggest an involvement of GATA-4 in the transcriptional regulation of CYP2C9. 10.1124/dmd.109

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2010

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Drug Metabolism and Disposition

  • ISSN

    0090-9556

  • e-ISSN

  • Volume of the periodical

    38

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

  • UT code for WoS article

    000274591400008

  • EID of the result in the Scopus database