C8ORF88: A Novel eIF4E-Binding Protein

Author:

Pugsley Lauren1ORCID,Naineni Sai Kiran1,Amiri Mehdi1,Yanagiya Akiko2ORCID,Cencic Regina1,Sonenberg Nahum13ORCID,Pelletier Jerry13

Affiliation:

1. Department of Biochemistry, McGill University, Montreal, QC H3G 1Y6, Canada

2. Arcalis, Inc., Kashiwa 277-0871, Japan

3. Rosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC H3A 1A3, Canada

Abstract

Translation initiation in eukaryotes is regulated at several steps, one of which involves the availability of the cap binding protein to participate in cap-dependent protein synthesis. Binding of eIF4E to translational repressors (eIF4E-binding proteins [4E-BPs]) suppresses translation and is used by cells to link extra- and intracellular cues to protein synthetic rates. The best studied of these interactions involves repression of translation by 4E-BP1 upon inhibition of the PI3K/mTOR signaling pathway. Herein, we characterize a novel 4E-BP, C8ORF88, whose expression is predominantly restricted to early spermatids. C8ORF88:eIF4E interaction is dependent on the canonical eIF4E binding motif (4E-BM) present in other 4E-BPs. Whereas 4E-BP1:eIF4E interaction is dependent on the phosphorylation of 4E-BP1, these sites are not conserved in C8ORF88 indicating a different mode of regulation.

Funder

Canadian Institutes of Health Research

Arcalis Inc.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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