| Literature DB >> 26371376 |
Massimiliano Clamer1, Toma Tebaldi2, Marta Marchioretto3, Paola Bernabò3, Efrem Bertini2, Graziano Guella4, Mauro Dalla Serra3, Alessandro Quattrone2, Gabriella Viero5.
Abstract
Genome-wide analyses of translation can provide major contributions in our understanding of the complex interplay between virulent factors and host cells. So far, the activation of host translational control mechanisms by bacterial toxins, owing to specific recruitment of mRNAs, RNA-binding proteins (RBPs) and ncRNAs (non-coding RNAs), are far from being understood. In the present study, we characterize for the first time the changes experienced by the translational control system of host cells in response to the well-known Staphylococcus aureus α-haemolysin (AHL) under both sublytic and lytic conditions. By comparing variations occurring in the cellular transcriptome and translatome, we give evidence that global gene expression is primarily rewired at the translational level, with the contribution of the RBP ELAVL1 (HuR) in the sublytic response. These results reveal the importance of translational control during host-pathogen interaction, opening new approaches for AHL-induced diseases.Entities:
Keywords: HuR; RNA-binding protein; bacterial toxins; polysomal profiling; pore-forming toxins; transcriptome; translational control; translatome
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Year: 2015 PMID: 26371376 DOI: 10.1042/BJ20150284
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857