The structure of a human translation initiation complex reveals two independent roles for the helicase eIF4A

Nat Struct Mol Biol. 2024 Mar;31(3):455-464. doi: 10.1038/s41594-023-01196-0. Epub 2024 Jan 29.

Abstract

Eukaryotic translation initiation involves recruitment of the 43S pre-initiation complex to the 5' end of mRNA by the cap-binding complex eIF4F, forming the 48S translation initiation complex (48S), which then scans along the mRNA until the start codon is recognized. We have previously shown that eIF4F binds near the mRNA exit channel of the 43S, leaving open the question of how mRNA secondary structure is removed as it enters the mRNA channel on the other side of the 40S subunit. Here we report the structure of a human 48S that shows that, in addition to the eIF4A that is part of eIF4F, there is a second eIF4A helicase bound at the mRNA entry site, which could unwind RNA secondary structures as they enter the 48S. The structure also reveals conserved interactions between eIF4F and the 43S, probaby explaining how eIF4F can promote mRNA recruitment in all eukaryotes.

MeSH terms

  • Codon, Initiator / metabolism
  • DNA Helicases / metabolism
  • Eukaryotic Initiation Factor-4A / chemistry
  • Eukaryotic Initiation Factor-4A / genetics
  • Eukaryotic Initiation Factor-4A / metabolism
  • Eukaryotic Initiation Factor-4F* / genetics
  • Eukaryotic Initiation Factor-4F* / metabolism
  • Humans
  • Peptide Chain Initiation, Translational*
  • Protein Biosynthesis
  • RNA, Messenger / metabolism
  • Ribosomes / metabolism

Substances

  • Eukaryotic Initiation Factor-4F
  • RNA, Messenger
  • Codon, Initiator
  • DNA Helicases
  • Eukaryotic Initiation Factor-4A