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A Viral mRNA Motif at the 3′-Untranslated Region that Confers Translatability in a Cell-Specific Manner. Implications for Virus Evolution

Author
Garcia-Moreno, Manuel; Sanz, Miguel Angel; Carrasco, Luis
Entity
UAM. Departamento de Biología Molecular
Publisher
Nature Publishing Group
Date
2016-01-12
Citation
10.1038/srep19217
Scientific Reports 6 (2016): 19217
 
 
 
ISSN
2045-2322
DOI
10.1038/srep19217
Funded by
This work was supported by a DGICYT (Dirección General de Investigación Científica y Técnica. Ministerio de Economía y Competitividad, Spain) grant BFU2012-31861. The Institutional Grant awarded to the Centro de Biología Molecular “Severo Ochoa” (CSIC-UAM) by the Fundación Ramón Areces is acknowledged
Project
Gobierno de España. BFU2012-31861
Editor's Version
http://dx.doi.org/10.1038/srep19217
Subjects
3' untranslated region; Antibody specificity; Protein biosynthesis; Nucleotide motifs; Biología y Biomedicina / Biología
URI
http://hdl.handle.net/10486/679300
Rights
© The Author(s) 2016

Licencia Creative Commons
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.

Abstract

Sindbis virus (SINV) mRNAs contain several motifs that participate in the regulation of their translation. We have discovered a motif at the 3′ untranslated region (UTR) of viral mRNAs, constituted by three repeated sequences, which is involved in the translation of both SINV genomic and subgenomic mRNAs in insect, but not in mammalian cells. These data illustrate for the first time that an element present at the 3′-UTR confers translatability to mRNAs from an animal virus in a cell-specific manner. Sequences located at the beginning of the 5′-UTR may also regulate SINV subgenomic mRNA translation in both cell lines in a context of infection. Moreover, a replicon derived from Sleeping disease virus, an alphavirus that have no known arthropod vector for transmission, is much more efficient in insect cells when the repeated sequences from SINV are inserted at its 3′-UTR, due to the enhanced translatability of its mRNAs. Thus, these findings provide a clue to understand, at the molecular level, the evolution of alphaviruses and their host range
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