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Suh, Pann-Ghill
BioSignal Network Lab (BSN)
Research Interests
  • Signal transduction, cancer, metabolism, phospholipase C

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Crosstalk between Src and major vault protein in epidermal growth factor-dependent cell signalling

Cited 25 times inthomson ciCited 25 times inthomson ci
Title
Crosstalk between Src and major vault protein in epidermal growth factor-dependent cell signalling
Author
Kim, ELee, SMian, MFYun, SUSong, MYi, KSRyu, SHSuh, Pann-Ghill
Keywords
ERK signaling pathway; MVP; Src; Src activity; Tyrosine phophorylation
Issue Date
200602
Publisher
WILEY-BLACKWELL
Citation
FEBS JOURNAL, v.273, no.4, pp.793 - 804
Abstract
Vaults are highly conserved, ubiquitous ribonucleoprotein (RNP) particles with an unidentified function. For the three protein species (TEP1, VPARP, and MVP) and a small RNA that comprises vault, expression of the unique 100-kDa major vault protein (MVP) is sufficient to form the basic vault structure. q1To identify and characterize proteins that interact with the Src homology 2 (SH2) domain of Src and potentially regulate Src activity, we used a pull-down assay using GST-Src-SH2 fusion proteins. We found MVP as a Src-SH2 binding protein in human stomach tissue. Interaction of Src and MVP was also observed in 253J q2stomach cancer cells. A subcellular localization study using immunofluorescence microscopy shows that epidermal growth factor (EGF) stimulation triggers MVP translocation from the nucleus to the cytosol and perinuclear region where it colocalizes with Src. We found that the interaction between Src and MVP is critically dependent on Src activity and protein (MVP) tyrosyl phosphorylation, which are induced by EGF stimulation. Our results also indicate MVP to be a novel substrate of Src and phosphorylated in an EGF-dependent manner. Interestingly, purified MVP inhibited the in vitro tyrosine kinase activity of Src in a concentration-dependent manner. MVP overexpression downregulates EGF-dependent ERK activation in Src overexpressing cells. To our knowledge, this is the first report of MVP interacting with a protein tyrosine kinase involved in a distinct cell signalling pathway. It appears that MVP is a novel regulator of Src-mediated signalling cascades.
URI
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DOI
http://dx.doi.org/10.1111/j.1742-4658.2006.05112.x
ISSN
1742-464X
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