Intersectin (ITSN) Regulation of Epidermal Growth Factor Receptor (EGFR) Ubiquitylation
Okur, Mustafa N.
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Ubiquitylation of receptor tyrosine kinases (RTKs) plays a critical role in regulating their trafficking and lysosomal degradation. Our laboratory identified the multi-domain scaffolding protein intersectin 1 (ITSN1) as an important regulator of this process. ITSN1 stimulates ubiquitylation of the epidermal growth factor receptor (EGFR) through enhancing the activity of Cbl E3 ubiquitin ligase. However, the precise mechanism through which ITSN1 enhances Cbl activity is unclear. My dissertation work here revealed a novel interaction of ITSN1 with two proteins, Spry2 and Shp2, involved in this Cbl-mediated EGFR ubiquitylation mechanism. With this study, I discovered that ITSN1 recruits Shp2 to Spry2 to enhance Spry2 tyrosine dephosphorylation, thereby blocking Spry2 interaction with Cbl and Spry2 inhibiton of Cbl activity for EGFR ubiquitylation. In addition, I also found that disruption of ITSN1 binding to Spry2 through point mutation of the Pro-rich ITSN1 binding site in Spry2 resulted in decreased Shp2:Spry2 interaction and enhanced Spry2 tyrosine phosphorylation, probably due to increased Shp2 sequestration. Although I mostly analyzed the effect of forced expression of these proteins on the mechanism, results obtained from my work are mechanistically quite informative. This study demonstrates that ITSN1 enhances Cbl activity, in part, by modulating the interaction of Cbl with Spry2 through recruitment of Shp2 phosphatase to the Cbl-Spry2.
Cysteine rich domain
A calcium-binding EF hand
Epidermal growth factor
Epidermal growth factor receptor
A small linker domain
Mitogen activated protein kinase
Non-small-cell lung cancer
A ring finger
Really interesting new gene
Receptor tyrosine kinase
Src homology 2
Src homology 3
SH2 domain containing phosphatases
Tyrosine kinase binding
Date available in INDIGO2016-02-25T10:30:08Z
Showing items related by title, author, creator and subject.
Klein, Irene K. (2009)
Intersectin 1 Enhances Cbl Ubiquitylation of Epidermal Growth Factor Receptor through Regulation of Sprouty2-Cbl Interaction Okur, Mustafa Nazir; Doi, Jolene; Fong, Chee Wai; Martinez, Natalia; Garcia-Dominguez, Carlota; Rojas, Jose M.; Guy, Graeme; O'Bryana, John P. (American Society for Microbiology, 2012-02)Ubiquitylation of receptor tyrosine kinases plays a critical role in regulating the trafficking and lysosomal degradation of these important signaling molecules. We identified the multidomain scaffolding protein intersectin ...
Wong, Katy A.; Wilson, Jessica; Russo, Angela; Wang, Li; Okur, Mustafa Nazir; Wang, Xuerong; Martin, Negin P.; Scappini, Erica; Carnegie, Graeme K.; O’Bryan, John P. (Public Library of Science, 2012-04)Members of the intersectin (ITSN) family of scaffold proteins consist of multiple modular domains, each with distinct ligand preferences. Although ITSNs were initially implicated in the regulation of endocytosis, subsequent ...