The pathway of hepatitis C virus mRNA recruitment to the human ribosome

Nat Struct Mol Biol. 2009 Apr;16(4):397-404. doi: 10.1038/nsmb.1572. Epub 2009 Mar 15.


Eukaryotic protein synthesis begins with mRNA positioning in the ribosomal decoding channel in a process typically controlled by translation-initiation factors. Some viruses use an internal ribosome entry site (IRES) in their mRNA to harness ribosomes independently of initiation factors. We show here that a ribosome conformational change that is induced upon hepatitis C viral IRES binding is necessary but not sufficient for correct mRNA positioning. Using directed hydroxyl radical probing to monitor the assembly of IRES-containing translation-initiation complexes, we have defined a crucial step in which mRNA is stabilized upon initiator tRNA binding. Unexpectedly, however, this stabilization occurs independently of the AUG codon, underscoring the importance of initiation factor-mediated interactions that influence the configuration of the decoding channel. These results reveal how an IRES RNA supplants some, but not all, of the functions normally carried out by protein factors during initiation of protein synthesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hepacivirus / physiology*
  • Humans
  • Nucleic Acid Conformation*
  • RNA, Messenger / metabolism*
  • RNA, Ribosomal, 18S / chemistry
  • RNA, Ribosomal, 18S / metabolism*
  • RNA, Transfer, Met / metabolism
  • RNA, Viral / metabolism*
  • Ribosomes / chemistry
  • Ribosomes / metabolism*


  • RNA, Messenger
  • RNA, Ribosomal, 18S
  • RNA, Transfer, Met
  • RNA, Viral