eIF2B: recent structural and functional insights into a key regulator of translation
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Monitoring eIF4F Assembly by Measuring eIF4E-eIF4G Interaction in Live Cells
Published on: May 1, 2020
Noel C Wortham1, Christopher G Proud2
1University of Southampton, Centre for Biological Sciences, Life Sciences Building 85, Highfield Campus, Southampton SO17 1BJ, U.K. Trafalgar School, London Road, Hilsea, Portsmouth, Hampshire, PO2 9RJ, U.K. nwortham@trafalgarschool.org.uk.
Abstract:
The eukaryotic translation initiation factor (eIF) eIF2B is a key regulator of mRNA translation, being the guanine nt exchange factor (GEF) responsible for the recycling of the heterotrimeric G-protein, eIF2, which is required to allow translation initiation to occur. Unusually for a GEF, eIF2B is a multi-subunit protein, comprising five different subunits termed α through ε in order of increasing size. eIF2B is subject to tight regulation in the cell and may also serve additional functions. Here we review recent insights into the subunit organization of the mammalian eIF2B complex, gained both from structural studies of the complex and from studies of mutations of eIF2B that result in the neurological disorder leukoencephalopathy with vanishing white matter (VWM). We will also discuss recent data from yeast demonstrating a novel function of the eIF2B complex key for translational regulation.
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