| Literature DB >> 34608523 |
Bingtian Shi1,2, Qinqin Song1,2, Xiaonuan Luo3, Juan Song1,2, Dong Xia1,2, Zhiqiang Xia1,2, Mi Liu1,2, Wenjun Wang1,2, Ruifang Wang1,2, Haijun Du1,2, Jun Han4,5.
Abstract
Internal ribosome entry site (IRES)-dependent translation is a mechanism distinct from 5' cap-dependent translation. IRES elements are located mainly in the 5' untranslated regions (UTRs) of viral and eukaryotic mRNAs. However, IRESs are also found in the coding regions of some viral and eukaryotic genomes to initiate the translation of some functional truncated isoforms. Here, five putative IRES elements of human rhinovirus 16 (HRV16) were identified in the coding region of the nonstructural proteins P2 and P3 through fusion with green fluorescent protein (GFP) expression vectors and bicistronic vectors with a hairpin structure. These five putative IRESs were located at nucleotide positions 4286-4585, 5002-5126, 6245-6394, 6619-6718, and 6629-6778 in the HRV16 genome. The functionality of the five IRESs was confirmed by their ability to initiate GFP expression in vitro. This suggests that an alternative mechanism might be used to increase the efficiency of replication of HRV16.Entities:
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Year: 2021 PMID: 34608523 DOI: 10.1007/s00705-021-05209-5
Source DB: PubMed Journal: Arch Virol ISSN: 0304-8608 Impact factor: 2.574