|ZFIN ID: ZDB-PUB-080616-26|
Comparative phosphoproteomics of zebrafish Fyn/Yes morpholino knockdown embryos
Lemeer, S., Jopling, C., Gouw, J.W., Mohammed, S., Heck, A.J., Slijper, M., and den Hertog, J.
|Source:||Molecular & cellular proteomics : MCP 7(11): 2176-2187 (Journal)|
|Registered Authors:||den Hertog, Jeroen, Jopling, Chris, Lemeer, Simone|
|PubMed:||18550893 Full text @ Mol. Cell. Proteomics|
Lemeer, S., Jopling, C., Gouw, J.W., Mohammed, S., Heck, A.J., Slijper, M., and den Hertog, J. (2008) Comparative phosphoproteomics of zebrafish Fyn/Yes morpholino knockdown embryos. Molecular & cellular proteomics : MCP. 7(11):2176-2187.
ABSTRACTThe coordinated movement of cells is indispensable for normal vertebrate gastrulation. Several important players and signaling pathways have been identified in convergence and extension (CE) cell movements during gastrulation, including non-canonical Wnt signaling. Fyn and Yes, members of the Src family of kinases, are key regulators of CE movements as well. Here we investigated signaling pathways in early development by comparison of the phosphoproteome of wild type zebrafish embryos with Fyn/Yes knockdown embryos that display specific CE cell movement defects. For quantitation we used differential stable isotope labeling by reductive amination of peptides. Equal amounts of labeled peptides from wild type and Fyn/Yes knockdown embryos were mixed and analyzed on an online RP-TiO2-RP-LC-MS/MS. Phosphorylated and non-phosphorylated peptides were quantified and significant changes in protein expression and/or phosphorylation were detected. We identified 348 phosphoproteins of which 69 showed a decrease in phosphorylation in Fyn/Yes knockdown embryos and 72 showed an increase in phosphorylation. Among these phosphoproteins were known regulators of cell movements, including Adducin and PDLIM5. Our results indicate that quantitative phosphoproteomics, combined with morpholino-mediated knockdowns can be used to identify novel signaling pathways that act in zebrafish development in vivo.