A widespread alternate form of cap-dependent mRNA translation initiation

Columba Parra, Amanda Ernlund, Amandine Alard, Kelly Ruggles, Beatrix Ueberheide and Robert J. Schneider ()
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Columba Parra: NYU School of Medicine
Amanda Ernlund: NYU School of Medicine
Amandine Alard: NYU School of Medicine
Kelly Ruggles: NYU School of Medicine
Beatrix Ueberheide: NYU School of Medicine
Robert J. Schneider: NYU School of Medicine

Nature Communications, 2018, vol. 9, issue 1, 1-9

Abstract: Abstract Translation initiation of most mammalian mRNAs is mediated by a 5′ cap structure that binds eukaryotic initiation factor 4E (eIF4E). However, inactivation of eIF4E does not impair translation of many capped mRNAs, suggesting an unknown alternate mechanism may exist for cap-dependent but eIF4E-independent translation. We show that DAP5, an eIF4GI homolog that lacks eIF4E binding, utilizes eIF3d to facilitate cap-dependent translation of approximately 20% of mRNAs. Genome-wide transcriptomic and translatomic analyses indicate that DAP5 is required for translation of many transcription factors and receptor capped mRNAs and their mRNA targets involved in cell survival, motility, DNA repair and translation initiation, among other mRNAs. Mass spectrometry and crosslinking studies demonstrate that eIF3d is a direct binding partner of DAP5. In vitro translation and ribosome complex studies demonstrate that DAP5 and eIF3d are both essential for eIF4E-independent capped-mRNA translation. These studies disclose a widespread and previously unknown mechanism for cap-dependent mRNA translation by DAP5-eIF3d complexes.

Date: 2018
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DOI: 10.1038/s41467-018-05539-0

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