Fiche publication
Date publication
juillet 2017
Journal
G3 (Bethesda, Md.)
Auteurs
Membres identifiés du Cancéropôle Est :
Mr HAMMANN Philippe
,
Pr IMLER Jean-Luc
,
Dr MEIGNIN Carine
Tous les auteurs :
Kuhn L, Majzoub K, Einhorn E, Chicher J, Pompon J, Imler JL, Hammann P, Meignin C
Lien Pubmed
Résumé
Receptor for Activated protein C kinase 1 (RACK1) is a scaffold protein that has been found in association with several signaling complexes, and with the 40S subunit of the ribosome. Using the model organism , we recently showed that RACK1 is required at the ribosome for internal ribosome entry site (IRES)-mediated translation of viruses. Here, we report a proteomic characterization of the interactome of RACK1 in S2 cells. We carried out Label-Free quantitation using both Data-Dependent and Data-Independent Acquisition (DDA and DIA, respectively) and observed a significant advantage for the Sequential Window Acquisition of all THeoretical fragment-ion spectra (SWATH) method, both in terms of identification of interactants and quantification of low abundance proteins. These data represent the first SWATH spectral library available for and will be a useful resource for the community. A total of 52 interacting proteins were identified, including several molecules involved in translation such as structural components of the ribosome, factors regulating translation initiation or elongation, and RNA binding proteins. Among these 52 proteins, 15 were identified as partners by the SWATH strategy only. Interestingly, these 15 proteins are significantly enriched for the functions translation and nucleic acid binding. This enrichment reflects the engagement of RACK1 at the ribosome and highlights the added value of SWATH analysis. A functional screen did not reveal any protein sharing the interesting properties of RACK1, which is required for IRES-dependent translation and not essential for cell viability. Intriguingly however, 10 of the RACK1 partners identified restrict replication of Cricket paralysis virus (CrPV), an IRES-containing virus.
Mots clés
Animals, Cell Line, Dicistroviridae, genetics, Drosophila Proteins, genetics, Drosophila melanogaster, Gene Regulatory Networks, Internal Ribosome Entry Sites, Models, Genetic, Protein Biosynthesis, genetics, Receptors for Activated C Kinase, genetics, Viral Proteins, biosynthesis
Référence
G3 (Bethesda). 2017 Jul 5;7(7):2249-2258
