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N6-methyladenosine in 5′ UTR does not promote translation initiation

2024; Elsevier BV; Volume: 84; Issue: 3 Linguagem: Inglês

10.1016/j.molcel.2023.12.028

1097-4164

Ewelina Guca, Rodrigo Alarcon, Michael Z. Palo, Leonardo Santos, Santiago Alonso‐Gil, Marcos Davyt, Leonardo Henrique França de Lima, Fanny Boissier, Sarada Das, Bojan Žagrović, Joseph D. Puglisi, Yaser Hashem, Zoya Ignatova,

Cancer-related gene regulation

The most abundant N6-methyladenosine (m6A) modification on mRNAs is installed non-stoichiometrically across transcripts, with 5′ untranslated regions (5′ UTRs) being the least conductive. 5′ UTRs are essential for translation initiation, yet the molecular mechanisms orchestrated by m6A remain poorly understood. Here, we combined structural, biochemical, and single-molecule approaches and show that at the most common position, a single m6A does not affect translation yields, the kinetics of translation initiation complex assembly, or start codon recognition both under permissive growth and following exposure to oxidative stress. Cryoelectron microscopy (cryo-EM) structures of the late preinitiation complex reveal that m6A purine ring established stacking interactions with an arginine side chain of the initiation factor eIF2α, although with only a marginal energy contribution, as estimated computationally. These findings provide molecular insights into m6A interactions with the initiation complex and suggest that the subtle stabilization is unlikely to affect the translation dynamics under homeostatic conditions or stress.