Src phosphorylation of cortactin enhances actin assembly

Shandiz Tehrani, Nenad Tomasevic, Scott Weed, Roman Sakowicz, John A. Cooper

Research output: Contribution to journalArticle

153 Scopus citations

Abstract

Src kinase mediates growth factor signaling and causes oncogenic transformation, which includes dramatic changes in the actin cytoskeleton, cell shape, and motility. Cortactin was discovered as a substrate for Src. How phosphorylation of cortactin can enhance actin assembly is unknown. Here, using an actin assembly system reconstituted from purified components, we demonstrate for the first time a biochemical mechanism by which Src phosphorylation of cortactin affects actin assembly. The adaptor Nck is an important component of the system, linking phosphorylated cortactin with neuronal WASp (N-WASp) and WASp-interacting protein (WIP) to activate Arp2/3 complex.

Original languageEnglish (US)
Pages (from-to)11933-11938
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume104
Issue number29
DOIs
StatePublished - Jul 17 2007

Keywords

  • N-WASp
  • Nck
  • Tyrosine phosphorylation

ASJC Scopus subject areas

  • General

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