Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/99187
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Type: Journal article
Title: ABC50 mutants modify translation start codon selection
Author: Stewart, J.
Cowan, J.
Perry, L.
Coldwell, M.
Proud, C.
Citation: Biochemical Journal, 2015; 467(2):217-229
Publisher: Portland Press
Issue Date: 2015
ISSN: 0264-6021
1470-8728
Statement of
Responsibility: 
Joanna D. Stewart, Joanne L. Cowan, Lisa S. Perry, Mark J. Coldwell and Christopher G. Proud
Abstract: ATP-binding cassette 50 (ABC50; also known as ABCF1) binds to eukaryotic initiation factor 2 (eIF2) and is required for efficient translation initiation. An essential step of this process is accurate recognition and selection of the initiation codon. It is widely accepted that the presence and movement of eIF1, eIF1A and eIF5 are key factors in modulating the stringency of start-site selection, which normally requires an AUG codon in an appropriate sequence context. In the present study, we show that expression of ABC50 mutants, which cannot hydrolyse ATP, decreases general translation and relaxes the discrimination against the use of non-AUG codons at translation start sites. These mutants do not appear to alter the association of key initiation factors to 40S subunits. The stringency of start-site selection can be restored through overexpression of eIF1, consistent with the role of that factor in enhancing stringency. The present study indicates that interfering with the function of ABC50 influences the accuracy of initiation codon selection.
Keywords: Translation initiation; eIF2; ABCF1; Start codon; Accuracy; Initiation factor
Rights: © The Authors. Journal compilation © 2015 Biochemical Society
RMID: 0030028850
DOI: 10.1042/BJ20141453
Appears in Collections:Biochemistry publications

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