| Literature DB >> 28433538 |
Baptiste Panthu1, Olivier Terrier2, Coralie Carron2, Aurélien Traversier2, Antoine Corbin1, Laurent Balvay1, Bruno Lina2, Manuel Rosa-Calatrava2, Théophile Ohlmann3.
Abstract
The non-structural protein NS1 of influenza A viruses exerts pleiotropic functions during infection. Among these functions, NS1 was shown to be involved in the control of both viral and cellular translation; however, the mechanism by which this occurs remains to be determined. Thus, we have revisited the role of NS1 in translation by using a combination of influenza infection, mRNA reporter transfection, and in vitro functional and biochemical assays. Our data show that the NS1 protein is able to enhance the translation of virtually all tested mRNAs with the exception of constructs bearing the Dicistroviruses Internal ribosome entry segment (IRESes) (DCV and CrPV), suggesting a role at the level of translation initiation. The domain of NS1 required for translation stimulation was mapped to the RNA binding amino-terminal motif of the protein with residues R38 and K41 being critical for activity. Although we show that NS1 can bind directly to mRNAs, it does not correlate with its ability to stimulate translation. This activity rather relies on the property of NS1 to associate with ribosomes and to recruit them to target mRNAs.Entities:
Keywords: NS1; RNA; influenza; ribosome; translation
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Year: 2017 PMID: 28433538 DOI: 10.1016/j.jmb.2017.04.007
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469