Eapen Vinay V, Waterman David P, Bernard Amélie, Schiffmann Nathan, Sayas Enrich, Kamber Roarke, Lemos Brenda, Memisoglu Gonen, Ang Jessie, Mazella Allison, Chuartzman Silvia G, Loewith Robbie J, Schuldiner Maya, Denic Vladimir, Klionsky Daniel J, Haber James E
Department of Biology, Brandeis University, Waltham, MA 02454.
Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Proc Natl Acad Sci U S A. 2017 Feb 14;114(7):E1158-E1167. doi: 10.1073/pnas.1614364114. Epub 2017 Feb 2.
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.
自噬通过控制各种DNA修复和检查点蛋白的水平在DNA损伤反应(DDR)中发挥核心作用;然而,DDR如何与自噬途径进行通信仍不清楚。利用芽殖酵母,我们证明全局基因毒性损伤甚至单个未修复的双链断裂(DSB)会启动一条以前未描述的选择性自噬途径,我们将其称为基因毒素诱导的靶向自噬(GTA)。GTA主要需要Mec1/ATR和Rad53/CHEK2检查点激酶的作用,部分是通过自噬核心蛋白的转录上调。GTA不同于饥饿诱导的自噬。GTA需要Atg11,这是选择性自噬机制的核心组成部分,但与先前描述的自噬途径不同。通过筛选约6000个酵母突变体的集合,我们鉴定出了控制GTA但对雷帕霉素诱导的自噬没有显著影响的基因。总体而言,我们的发现建立了一条特定于DNA损伤反应的自噬途径。