| Literature DB >> 25635050 |
Maria Teresa Almeida1, Francisco S Mesquita2, Rui Cruz1, Hugo Osório3, Rafael Custódio4, Cláudia Brito1, Didier Vingadassalom5, Mariana Martins4, John M Leong5, David W Holden6, Didier Cabanes7, Sandra Sousa8.
Abstract
Bacterial pathogens often interfere with host tyrosine phosphorylation cascades to control host responses and cause infection. Given the role of tyrosine phosphorylation events in different human infections and our previous results showing the activation of the tyrosine kinase Src upon incubation of cells with Listeria monocytogenes, we searched for novel host proteins undergoing tyrosine phosphorylation upon L. monocytogenes infection. We identify the heavy chain of the non-muscle myosin IIA (NMHC-IIA) as being phosphorylated in a specific tyrosine residue in response to L. monocytogenes infection. We characterize this novel post-translational modification event and show that, upon L. monocytogenes infection, Src phosphorylates NMHC-IIA in a previously uncharacterized tyrosine residue (Tyr-158) located in its motor domain near the ATP-binding site. In addition, we found that other intracellular and extracellular bacterial pathogens trigger NMHC-IIA tyrosine phosphorylation. We demonstrate that NMHC-IIA limits intracellular levels of L. monocytogenes, and this is dependent on the phosphorylation of Tyr-158. Our data suggest a novel mechanism of regulation of NMHC-IIA activity relying on the phosphorylation of Tyr-158 by Src.Entities:
Keywords: Cellular Infection; Gram-positive Bacteria; Host-Pathogen Interaction; Intracellular Bacterial Pathogen; Listeria monocytogenes; Myosin; Non-muscle Myosin IIA; Phosphotyrosine Signaling; Post-translational Modification; Src
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Year: 2015 PMID: 25635050 PMCID: PMC4375491 DOI: 10.1074/jbc.M114.591313
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157