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Biochem Biophys Res Commun ; 290(3): 1030-6, 2002 Jan 25.
Article in English | MEDLINE | ID: mdl-11798178

ABSTRACT

Overexpression of the 5T4 transmembrane glycoprotein can have marked effects on both the actin cytoskeleton and cell migration. Using a yeast two-hybrid approach, we describe a novel interaction between 5T4 and TIP-2/GIPC, a cytoplasmic interacting protein containing a PDZ domain. The cytoplasmic tail of 5T4 contains a class I PDZ-binding motif (Ser-Asp-Val) and we demonstrate that this region, in particular the terminal valine, is required for 5T4 interaction with TIP-2/GIPC. HeLa cells expressing hemagglutinin-tagged TIP-2/GIPC (HA-TIP-2/GIPC) have an altered distribution of endogenous 5T4, which colocalizes with HA-TIP-2/GIPC, thus supporting an interaction. Furthermore, TIP-2/GIPC can be coimmunoprecipitated with 5T4 from HeLa cell lysates. Identification of the 5T4 and TIP-2/GIPC interaction provides the first link between 5T4 and the actin cytoskeleton. Since other proteins, like 5T4, associate with TIP-2/GIPC and are linked with cancer, we explore the possibility that TIP-2/GIPC may be a common factor involved in the cancer process.


Subject(s)
Antigens, Neoplasm/metabolism , Carrier Proteins/metabolism , Membrane Glycoproteins/metabolism , Neuropeptides/metabolism , Adaptor Proteins, Signal Transducing , Amino Acid Motifs , Amino Acid Sequence , Antigens, Neoplasm/chemistry , Carrier Proteins/chemistry , HeLa Cells , Humans , Membrane Glycoproteins/chemistry , Membrane Glycoproteins/immunology , Microscopy, Fluorescence , Molecular Sequence Data , Neoplasm Metastasis , Neuropeptides/chemistry , Precipitin Tests , Protein Structure, Tertiary , Sequence Homology, Amino Acid , Two-Hybrid System Techniques , Yeasts/genetics
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