Control of Cell Survival and Proliferation by Mammalian Eukaryotic Initiation Factor 4B

Author:

Shahbazian David1,Parsyan Armen1,Petroulakis Emmanuel1,Topisirovic Ivan1,Martineau Yvan1,Gibbs Bernard F.2,Svitkin Yuri1,Sonenberg Nahum1

Affiliation:

1. Department of Biochemistry and Goodman Cancer Centre, McGill University, 1160 Pine Avenue West, Montreal, Quebec H3A 1A3, Canada

2. Department of Medicine, McGill University, Sheldon Biotechnology Center, MUHC Royal Victoria Hospital, 687 Pine Avenue West, Montreal, Quebec H3A 1A1, Canada

Abstract

ABSTRACT Translation initiation plays an important role in cell growth, proliferation, and survival. The translation initiation factor eIF4B (eukaryotic initiation factor 4B) stimulates the RNA helicase activity of eIF4A in unwinding secondary structures in the 5′ untranslated region (5′UTR) of the mRNA in vitro . Here, we studied the effects of eIF4B depletion in cells using RNA interference (RNAi). In agreement with the role of eIF4B in translation initiation, its depletion resulted in inhibition of this step. Selective reduction of translation was observed for mRNAs harboring strong to moderate secondary structures in their 5′UTRs. These mRNAs encode proteins, which function in cell proliferation (Cdc25C, c-myc, and ODC [ornithine decarboxylase]) and survival (Bcl-2 and XIAP [X-linked inhibitor of apoptosis]). Furthermore, eIF4B silencing led to decreased proliferation rates, promoted caspase-dependent apoptosis, and further sensitized cells to camptothecin-induced cell death. These results demonstrate that eIF4B is required for cell proliferation and survival by regulating the translation of proliferative and prosurvival mRNAs.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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