eIF3d specialized translation requires a RACK1-driven eIF3d binding to 43S PIC in proliferating SH-SY5Y neuroblastoma cells
Articolo
Data di Pubblicazione:
2025
Abstract:
Translation initiation of most mammalian mRNAs is mediated by a 5' cap structure that binds eukaryotic initiation factor 4E (eIF4E). Notably, most mRNAs are still capped when eIF4E is inhibited, suggesting alternative mechanisms likely mediate cap-dependent mRNA translation without functional eIF4F. Here we found that, when eIF4E is inhibited, the ribosomal scaffold RACK1 recruits eIF3d on the 43S pre-initiation complex. Moreover, we found that it is just PKCBII in its active form that promotes the binding of RACK1 to eIF3d. These studies disclose a previously unknown role of ribosomal RACK1 for eIF3d specialized translation.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Translation initiation of most mammalian mRNAs is mediated by a 5′ cap structure that binds eukaryotic initiation factor 4E (eIF4E). Notably; most mRNAs are still capped when eIF4E is inhibited; suggesting alternative mechanisms likely mediate cap-dependent mRNA translation without functional eIF4F. Here we found that; when eIF4E is inhibited; the ribosomal scaffold RACK1 recruits eIF3d on the 43S pre-initiation complex. Moreover; we found that it is just PKCBII in its active form that promotes the binding of RACK1 to eIF3d. These studies disclose a previously unknown role of ribosomal RACK1 for eIF3d specialized translation
Elenco autori:
Silvestri, Federica; Montuoro, Raffaele; Catalani, Elisabetta; Tilesi, Francesca; Willems, Daniela; Romano, Nicla; Ricciardi, Sara; Cervia, Davide; Ceci, Marcello
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