Hepatitis C virus internal ribosome entry site
| Hepatitis C virus internal ribosome entry site | |
|---|---|
 Predicted secondary structure and sequence conservation of IRES_HCV | |
| Identifiers | |
| Symbol | IRES_HCV |
| Alt. Symbols | HCV_IRES |
| Rfam | RF00061 |
| Other data | |
| RNA type | Cis-reg; IRES |
| Domain(s) | Viruses |
| GO | GO:0043022 |
| SO | SO:0000243 |
| PDB structures | PDBe |
The Hepatitis C virus internal ribosome entry site, or HCV IRES, is an RNA structure within the 5'UTR of the HCV genome that mediates cap-independent translation initiation.
Protein translation of most eukaryotic mRNAs occurs by a cap-dependent mechanism and requires association of Met-tRNAiMet, several eukaryotic initiation factors, and GTP with the 40S ribosomal subunit, recruitment to the 5' cap, and scanning along the 5' UTR to reach to start codon. In contrast, translation of hepatitis C virus (HCV) mRNA is initiated by a different mechanism from the usual 5' cap-binding model.[1] This alternate mechanism relies on the direct binding of the 40S ribosomal subunit by the internal ribosome entry site (IRES) in the 5' UTR of HCV RNA. The HCV IRES adopts a complex structure, and may differ significantly from IRES elements identified in picornaviruses. A small number of eukaryotic mRNAs has been shown to be translated by internal ribosome entry.[2][3]
IRES structure
[edit]Nucleotides 1–40 of the HCV mRNA are thought not to contribute to translation, and are rather required for genomic RNA replication. The remainder of the HCV 5'-UTR consists of three domains, namely domains II-IV (domain I is located on the 5'-end of the mRNA).[citation needed]
Mechanism of action
[edit]HCV IRES independently binds two components of eukaryotic translation initiation machinery, the multiprotein initiation factor eIF3 and 40S small ribosomal subunit. Moreover, it binds 40S in such a manner that AUG initiator codon is positioned in the ribosomal P-site, thus no ribosomal scanning is required. Consequently scanning factors eIF1 and eIF1A are dispensable for the HCV translation, as are components of the eIF4F complex (eIF4A, eIF4E, and eIF4G) and eIF4B, which are generally required for mRNA binding and unwinding of 5'UTR. Initiator tRNA is delivered either by eIF2 or, in stress conditions when eIF2 is inactivated, by eIF2A, eIF2D, or possibly eIF5B, a homologue of prokaryotic IF2 protein.[citation needed]
See also
[edit]References
[edit]- ^ Lytle JR, Wu L, Robertson HD (August 2002). "Domains on the hepatitis C virus internal ribosome entry site for 40s subunit binding". RNA. 8 (8): 1045–1055. doi:10.1017/S1355838202029965. PMC 1370315. PMID 12212848.
- ^ Beales LP, Rowlands DJ, Holzenburg A (May 2001). "The internal ribosome entry site (IRES) of hepatitis C virus visualized by electron microscopy". RNA. 7 (5): 661–670. doi:10.1017/S1355838201001406. PMC 1370118. PMID 11350030.
- ^ Gallego J, Varani G (April 2002). "The hepatitis C virus internal ribosome-entry site: a new target for antiviral research". Biochemical Society Transactions. 30 (2): 140–145. doi:10.1042/BST0300140. PMID 12023841.
Further reading
[edit]- Malygin AA, Kossinova OA, Shatsky IN, Karpova GG (October 2013). "HCV IRES interacts with the 18S rRNA to activate the 40S ribosome for subsequent steps of translation initiation". Nucleic Acids Research. 41 (18): 8706–8714. doi:10.1093/nar/gkt632. PMC 3794592. PMID 23873958.