Iterative tyrosine phosphorylation controls non-canonical domain utilization in Crk

G. Sriram, W. Jankowski, C. Kasikara, C. Reichman, T. Saleh, K. Q. Nguyen, J. Li, P. Hornbeck, K. Machida, T. Liu, H. Li, C. G. Kalodimos, R. B. Birge

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Crk, the prototypical member of a class of Src homology-2 (SH2) and Src homology-3 (SH3) domain containing proteins that controls the coordinated assembly of signaling complexes, is regulated by phosphorylation of Y221 in the linker region, which forms an intramolecular SH2-pY221 auto-clamp to interrupt SH2-N-terminal SH3 domain (SH3N) signaling. Here, we show using LC-MS/MS and by generating phospho-specific antibodies that, iteratively with Y221, the Crk C-terminal SH3 domain (SH3C) is routinely phosphorylated on Y239 and/or Y251 by several extracellular stimuli known to engage Crk. Although phosphorylation at Y221 auto-inhibits the Crk SH2, phosphorylation of the SH3C generates an unconventional phosphoSH3C-SH3N unit in which the SH3N is fully functional to bind polyproline type II ligands and the phosphoSH3C binds de novo to other SH2 domains. Using high-throughput SH2 domain profiling, artificial neural network and position-specific scoring matrix-based bioinformatics approaches, and unbiased mass spectometry, we found that the phosphoSH3C binds several SH2 domain containing proteins, including specific non-receptor tyrosine kinases-Abl via pY251 and C-terminal Src kinase via pY239. Functionally, we show that the phosphoSH3C modulates the Abl-mediated phenotypes of cell spreading and motility. Together, these studies describe a versatile mechanism wherein phosphorylation of Crk at Y221 is not an off switch but redirects signaling from the SH2-SH3N axis to a phosphoSH3C-SH3N axis, with the SH3N as a common denominator.

Original languageEnglish (US)
Pages (from-to)4260-4269
Number of pages10
JournalOncogene
Volume34
Issue number32
DOIs
StatePublished - Aug 6 2015

Bibliographical note

Funding Information:
This work was supported by the NIH grant CA165077 to RBB and Rutgers Foundation grant to RBB and in part by NIH grant to CGK and RBB GM080308. The LC-MS/MS work was funded in part by an NIH grant NS046593, for the support of the Rutgers Neuroproteomics Core Facility. We thank Chingiz Underbayev, WenI Tsou and Anita Antes for technical support; Sushil Kumar and Stanley Kimani for discussion.

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