Critical Contacts between the Eukaryotic Initiation Factor 2B (eIF2B) Catalytic Domain and both eIF2β and -2γ Mediate Guanine Nucleotide Exchange

Abstract

Diverse guanine nucleotide exchange factors (GEFs) regulate the activity of GTP binding proteins. One of the most complicated pairs is eukaryotic initiation factor 2B (eIF2B) and eIF2, which function during protein synthesis initiation in eukaryotes. We have mutated conserved surface residues within the eIF2B GEF domain, located at the eIF2Bε C terminus. Extensive genetic and biochemical characterization established how these residues contribute to GEF activity. We find that the universally conserved residue E569 is critical for activity and that even a conservative E569D substitution is lethal in vivo. Several mutations within residues close to E569 have no discernible effect on growth or GCN4 expression, but an alanine substitution at the adjacent L568 is cold sensitive and deregulates GCN4 activity at 15°C. The mutation of W699, found on a separate surface approximately 40 Å from E569, is also lethal. Binding studies show that W699 is critical for interaction with eIF2β, while L568 and E569 are not. In contrast, all three residues are critical for interaction with eIF2γ. These data show that multiple contacts between eIF2γ and eIF2Bε mediate nucleotide exchange.

SUPPLEMENTAL MATERIAL

We thank Thomas Jowitt at the University of Manchester FLS Biomolecular analysis facility for assistance with CD spectra; Thomas Boesen, Gregers Rom Andersen (University of Aarhus, Aarhus, Denmark), Mark Ashe (Manchester, United Kingdom), and other members of the Pavitt team for helpful discussions; and the anonymous reviewers for their suggestions.

This work was supported by grants to G.D.P. from The Wellcome Trust.