| Literature DB >> 26924586 |
Jiří Černý1,2,3, Martin Selinger4,5, Martin Palus4,5,6, Zuzana Vavrušková4, Hana Tykalová4,5, Lesley Bell-Sakyi7, Ján Štěrba4,5, Libor Grubhoffer4,5, Daniel Růžek4,6.
Abstract
A short upstream open reading frame (uORF) was recently identified in the 5' untranslated region of some tick-borne encephalitis virus (TBEV) strains. However, it is not known if the peptide encoded by TBEV uORF (TuORF) is expressed in infected cells. Here we show that TuORF forms three phylogenetically separated clades which are typical of European, Siberian, and Far-Eastern TBEV subtypes. Analysis of selection pressure acting on the TuORF area showed that it is under positive selection pressure. Theoretically, TuORF may code for a short hydrophobic peptide embedded in a biological membrane. However, expression of TuORF was detectable neither by immunoblotting in tick and mammalian cell lines infected with TBEV nor by immunofluorescence in TBEV-infected mammalian cell lines. These results support the idea that TuORF is not expressed in TBEV-infected cell or expressed in undetectably low concentrations. Therefore we can assume that TuORF has either minor or no biological role in the TBEV life cycle.Entities:
Keywords: Immunoblotting; Immunofluorescence; TBEV; TuORF; uORF
Mesh:
Year: 2016 PMID: 26924586 DOI: 10.1007/s11262-015-1273-y
Source DB: PubMed Journal: Virus Genes ISSN: 0920-8569 Impact factor: 2.332