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
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DOI - Digital Object Identifier
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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
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Czech description
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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
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Result continuities
Project
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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
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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
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UT code for WoS article
000274591400008
EID of the result in the Scopus database
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