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A more recent version of this article appeared on July 1, 2008
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Submitted on November 26, 2007
Revised on March 31, 2008
Accepted on April 9, 2008
The University of Manchester, Faculty of Life Sciences, Manchester M13 9PT, United Kingdom
Monitoring Editor: Thomas Fox
An oxidative stress occurs when reactive oxygen species overwhelm the cellular antioxidant defenses. We have examined the regulation of protein synthesis in S. cerevisiae in response to oxidative stress induced by exposure to hydroperoxides (hydrogen peroxide, cumene hydroperoxide), a thiol oxidant (diamide) and a heavy metal (cadmium). Examination of translational activity indicates that these oxidants inhibit translation at the initiation and post-initiation phases. Inhibition of translation initiation in response to hydroperoxides is entirely dependent on phosphorylation of the alpha subunit of eIF2 by the Gcn2 kinase. Activation of Gcn2 is mediated by uncharged tRNA since mutation of its HisRS domain abolishes regulation in response to hydroperoxides. Furthermore, Gcn4 is translationally up-regulated in response to H2O2 and is required for hydroperoxide resistance. We used transcriptional profiling to identify a wide-range of genes which mediate this response as part of the Gcn4-dependent H2O2-regulon. In contrast to hydroperoxides, regulation of translation initiation in response to cadmium and diamide depends on both Gcn2 and the eIF4E binding protein Eap1. Thus, the response to oxidative stress is mediated by oxidant-specific regulation of translation initiation and we suggest that this is an important mechanism underlying the ability of cells to adapt to different oxidants.