Translational Control of the Picornavirus Phenotype
- PMID: 32214465
- PMCID: PMC7089230
- DOI: 10.1023/A:1010531228348
Translational Control of the Picornavirus Phenotype
Abstract
Picornaviruses are small animal viruses with positive-strand genomic RNA, which is translated using cap-independent internal translation initiation. The key role in this is played by ciselements of the 5"-untranslated region (5"-UTR) and, in particular, by the internal ribosome entry site (IRES). The function of translational ciselements requires both canonical translation initiation factors (eIFs) and additional IRES trans-acting factors (ITAFs). All known ITAFs are cell RNA-binding proteins which play a variety of functions in noninfected cells. Specific features of translational ciselements substantially affect the phenotype and, in particular, tissue tropism and pathogenic properties of picornaviruses. It is clear that, in some cases, the molecular mechanism involved is a change in interactions between viral ciselements and ITAFs. The properties and tissue distribution of ITAFs may determine the biological properties of other viruses that also use the IRES-dependent translation initiation. Since this mechanism is also involved in translation of several cell mRNAs, ITAF may contribute to the regulation of the most important aspects of the living activity in noninfected cells.
Keywords: RNA-binding proteins; differentiation; translation factors; virulence; viruses.
© MAIK “Nauka/Interperiodica” 2001.
Similar articles
-
[Translational control of the picornavirus phenotype].Mol Biol (Mosk). 2001 Jul-Aug;35(4):691-701. Mol Biol (Mosk). 2001. PMID: 11524956 Review. Russian.
-
Advances and Breakthroughs in IRES-Directed Translation and Replication of Picornaviruses.mBio. 2023 Apr 25;14(2):e0035823. doi: 10.1128/mbio.00358-23. Epub 2023 Mar 20. mBio. 2023. PMID: 36939331 Free PMC article. Review.
-
hnRNP K Is a Novel Internal Ribosomal Entry Site-Transacting Factor That Negatively Regulates Foot-and-Mouth Disease Virus Translation and Replication and Is Antagonized by Viral 3C Protease.J Virol. 2020 Aug 17;94(17):e00803-20. doi: 10.1128/JVI.00803-20. Print 2020 Aug 17. J Virol. 2020. PMID: 32581104 Free PMC article.
-
A cell cycle-dependent protein serves as a template-specific translation initiation factor.Genes Dev. 2000 Aug 15;14(16):2028-45. Genes Dev. 2000. PMID: 10950867 Free PMC article.
-
Hepatitis C Virus Translation Regulation.Int J Mol Sci. 2020 Mar 27;21(7):2328. doi: 10.3390/ijms21072328. Int J Mol Sci. 2020. PMID: 32230899 Free PMC article. Review.
Cited by
-
Decay-accelerating factor binding determines the entry route of echovirus 11 in polarized epithelial cells.J Virol. 2011 Dec;85(23):12376-86. doi: 10.1128/JVI.00016-11. Epub 2011 Sep 14. J Virol. 2011. PMID: 21917947 Free PMC article.
References
LinkOut - more resources
Full Text Sources
Miscellaneous