Proceedings of the National Academy of Sciences · 2017 · 71 citations · 57 references
Life SciencesCell BiologyMolecular BiologyAutophagyCell SignalingMolecular Cell BiologyAutophagy In Stress ResponsesAutophagy ModulationAutophagy RegulationAutophagy Signaling PathwaysNutrient Sensing In AutophagySelective AutophagyAutophagy PathwayAutophagy Under StressCytoskeletal IntegrityDna Damage InductionDna Damage Response PathwaysDna Damage Response SignalingDna Damage SensorsYeast Autophagy
Autophagy plays a central role in the DNA damage response (DDR) by controlling the levels of various DNA repair and checkpoint proteins; however, how the DDR communicates with the autophagy pathway remains unknown. Using budding yeast, we demonstrate that global genotoxic damage or even a single unrepaired double-strand break (DSB) initiates a previously undescribed and selective pathway of autophagy that we term genotoxin-induced targeted autophagy (GTA). GTA requires the action primarily of Mec1/ATR and Rad53/CHEK2 checkpoint kinases, in part via transcriptional up-regulation of central autophagy proteins. GTA is distinct from starvation-induced autophagy. GTA requires Atg11, a central component of the selective autophagy machinery, but is different from previously described autophagy pathways. By screening a collection of ∼6,000 yeast mutants, we identified genes that control GTA but do not significantly affect rapamycin-induced autophagy. Overall, our findings establish a pathway of autophagy specific to the DNA damage response.
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