Abstract
Caloric restriction extends lifespan, an effect once thought to involve attenuation of reactive oxygen species (ROS) generated by aerobic metabolism. However, recent evidence suggests that caloric restriction may in fact raise ROS levels, which in turn provides protection from acute doses of oxidant through a process called adaptation. To shed light on the molecular mechanisms of adaptation, we designed a series of genome-wide deletion fitness and mRNA expression screens to identify genes involved in adaptation to hydrogen peroxide. Combined with known transcriptional interactions, the integrated data implicate Yap1 and Skn7 as central transcription factors of both the adaptive and acute oxidative responses. They also identify the transcription factors Mga2 and Rox1 as active exclusively in the adaptive response and show that Mga2 is essential for adaptation. These findings are striking because Mga2 and Rox1 have been thought to control the response to hypoxic, not oxidative, conditions. Expression profiling of mga2Δ and rox1Δ knockouts shows that these factors most strongly regulate targets in ergosterol, fatty-acid, and zinc metabolic pathways. Direct quantitation of ergosterol reveals that its basal concentration indeed depends on Mga2, but that Mga2 is not required for the decrease in ergosterol observed during adaptation.
Highlights
Oxidative stress is caused by a number of reactive oxygen species (ROS) generated as a result of aerobic metabolism or chemical exposure
We studied this process in order to identify the mechanisms that provide this protection
Our study identified a number of genes and processes with previously unappreciated roles in adaptation
Summary
Oxidative stress is caused by a number of reactive oxygen species (ROS) generated as a result of aerobic metabolism or chemical exposure. In one model of adaptation, the cell increases the activity of the enzymes and pathways required to rid the cells of ROS, leaving it better equipped to process acute dosages of oxidant when they arise. Genes involved in the adaptive response are expected to be a subset of those that become active in the acute response [15] Many such candidates have been identified, including a variety of biosynthetic enzymes which produce small molecular compounds or proteins with reduction potential, such as glutathione (GSH), thioredoxin, NADPH, and trehalose [16,17,18,19,20]. Machinery with a central role in the acute response, such as the mitochondria [9,32] or the Msn2/4 environmental stress response factors, are not required for adaptation [27,33]
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