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Translation of hepatitis C virus RNA
Author(s) -
Hellen C. U. T.,
Pestova T. V.
Publication year - 1999
Publication title -
journal of viral hepatitis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 100
eISSN - 1365-2893
pISSN - 1352-0504
DOI - 10.1046/j.1365-2893.1999.00150.x
Subject(s) - internal ribosome entry site , eukaryotic translation , initiation factor , eukaryotic initiation factor , eukaryotic small ribosomal subunit , biology , eif2 , eukaryotic translation initiation factor 4 gamma , start codon , five prime untranslated region , transcription preinitiation complex , genetics , eif4g , translation (biology) , virology , microbiology and biotechnology , messenger rna , gene , gene expression , promoter
The 341‐nucleotide 5’ non‐translated region is the most conserved part of the hepatitis C virus (HCV) genome. It contains a highly structured internal ribosomal entry site (IRES) that mediates cap‐independent initiation of translation of the viral polyprotein by a mechanism that is unprecedented in eukaryotes. The first step in translation initiation is assembly of eukaryotic initiation factor (eIF) 3, eIF2, GTP, initiator tRNA and a 40S ribosomal subunit into a 43S preinitiation complex. The HCV IRES recruits this complex and directs its precise attachment at the initiation codon to form a 48S complex in a process that does not involve eIFs 4A, 4B or 4F. The IRES contains sites that bind independently with the eIF3 and 40S subunit components of 43S complexes, and structural determinants that ensure the correct spatial orientation of these binding sites so that the 48S complex assembles precisely at the initiation codon.