TY - JOUR
T1 - The 5' and 3' ends of alphavirus RNAs - Non-coding is not non-functional
AU - Hyde, Jennifer L.
AU - Chen, Rubing
AU - Trobaugh, Derek W.
AU - Diamond, Michael S.
AU - Weaver, Scott C.
AU - Klimstra, William B.
AU - Wilusz, Jeffrey
N1 - Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/8/3
Y1 - 2015/8/3
N2 - The non-coding regions found at the 5' and 3' ends of alphavirus genomes regulate viral gene expression, replication, translation and virus-host interactions, which have significant implications for viral evolution, host range, and pathogenesis. The functions of these non-coding regions are mediated by a combination of linear sequence and structural elements. The capped 5' untranslated region (UTR) contains promoter elements, translational regulatory sequences that modulate dependence on cellular translation factors, and structures that help to avoid innate immune defenses. The polyadenylated 3' UTR contains highly conserved sequence elements for viral replication, binding sites for cellular miRNAs that determine cell tropism, host range, and pathogenesis, and conserved binding regions for a cellular protein that influences viral RNA stability. Nonetheless, there are additional conserved elements in non-coding regions of the virus (e.g., the repeated sequence elements in the 3' UTR) whose function remains obscure. Thus, key questions remain as to the function of these short yet influential untranslated segments of alphavirus RNAs.
AB - The non-coding regions found at the 5' and 3' ends of alphavirus genomes regulate viral gene expression, replication, translation and virus-host interactions, which have significant implications for viral evolution, host range, and pathogenesis. The functions of these non-coding regions are mediated by a combination of linear sequence and structural elements. The capped 5' untranslated region (UTR) contains promoter elements, translational regulatory sequences that modulate dependence on cellular translation factors, and structures that help to avoid innate immune defenses. The polyadenylated 3' UTR contains highly conserved sequence elements for viral replication, binding sites for cellular miRNAs that determine cell tropism, host range, and pathogenesis, and conserved binding regions for a cellular protein that influences viral RNA stability. Nonetheless, there are additional conserved elements in non-coding regions of the virus (e.g., the repeated sequence elements in the 3' UTR) whose function remains obscure. Thus, key questions remain as to the function of these short yet influential untranslated segments of alphavirus RNAs.
KW - Polyadenylation
KW - Protein-RNA interactions
KW - Translation regulation
KW - Viral pathogenesis
KW - mRNA capping
KW - miRNAs
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U2 - 10.1016/j.virusres.2015.01.016
DO - 10.1016/j.virusres.2015.01.016
M3 - Article
C2 - 25630058
AN - SCOPUS:84931570782
SN - 0168-1702
VL - 206
SP - 99
EP - 107
JO - Virus Research
JF - Virus Research
ER -