FEBS letters · 2007
Overexpression of the Rho-guanine nucleotide exchange factor ECT2 inhibits nuclear translocation of nuclear receptor CAR in the mouse liver.
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Hosseinpour Fardin, Timsit Yoav, Koike Chika, Matsui Kenji, Yamamoto Yukio, Moore Rick, Negishi Masahiko
Аннотация
Various drugs such as phenobarbital (PB) trigger translocation of constitutive active/adrostane receptor (CAR) from the cytoplasm into the nucleus of mouse liver cells without directly binding to the receptor. We have now characterized the guanine nucleotide exchange factor epithelial cell-transforming gene 2 (ECT2) as a PB-inducible factor as well as a cellular signal that represses PB-triggered nuclear translocation of CAR. When CFP-tagged ECT2 was co-expressed with YFP-tagged CAR in the liver of Car(-/-) mice, ECT2 repressed CAR nuclear translocation. Coexpression of various deletion mutants delineated this repressive activity to the tandem Dbl homology/pleckstrin homology domains of ECT2 and to their cytosolic expression. CAR directly bound to the PH domain. Thus, ECT2 may comprise a part of the PB response signal regulating the intracellular trafficking of CAR.
Предметные рубрики MeSH
Active Transport, Cell NucleusAnimalsBinding SitesCell Line, TumorCell NucleusConstitutive Androstane ReceptorGuanine Nucleotide Exchange FactorsHumansLiverMaleMiceMice, KnockoutPhenobarbitalProtein Structure, TertiaryProto-Oncogene ProteinsReceptors, Cytoplasmic and NuclearSequence DeletionTranscription FactorsTranscription, Genetic