Structure of a human 48 S translational initiation complex

Science. 2020 Sep 4;369(6508):1220-1227. doi: 10.1126/science.aba4904.

Abstract

A key step in translational initiation is the recruitment of the 43S preinitiation complex by the cap-binding complex [eukaryotic initiation factor 4F (eIF4F)] at the 5' end of messenger RNA (mRNA) to form the 48S initiation complex (i.e., the 48S). The 48S then scans along the mRNA to locate a start codon. To understand the mechanisms involved, we used cryo-electron microscopy to determine the structure of a reconstituted human 48S The structure reveals insights into early events of translation initiation complex assembly, as well as how eIF4F interacts with subunits of eIF3 near the mRNA exit channel in the 43S The location of eIF4F is consistent with a slotting model of mRNA recruitment and suggests that downstream mRNA is unwound at least in part by being "pulled" through the 40S subunit during scanning.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Codon, Initiator
  • Cryoelectron Microscopy
  • Eukaryotic Initiation Factor-3 / chemistry*
  • Eukaryotic Initiation Factor-4F / chemistry*
  • Humans
  • Hydrolysis
  • Peptide Chain Initiation, Translational*
  • RNA, Messenger / chemistry

Substances

  • Codon, Initiator
  • Eukaryotic Initiation Factor-3
  • Eukaryotic Initiation Factor-4F
  • RNA, Messenger
  • Adenosine Triphosphate