TY - JOUR
T1 - A pathway of targeted autophagy is induced by DNA damage in budding yeast
AU - Eapen, Vinay V.
AU - Waterman, David P.
AU - Bernard, Amelie
AU - Schiffmann, Nathan
AU - Sayas, Enrich
AU - Kamber, Roarke
AU - Lemos, Brenda
AU - Memisoglu, Gonen
AU - Ang, Jessie
AU - Mazella, Allison
AU - Chuartzman, Silvia G.
AU - Loewith, Robbie J.
AU - Schuldiner, Maya
AU - Denic, Vladimir
AU - Klionsky, Daniel J.
AU - Haber, James E.
N1 - Publisher Copyright: © 2017, National Academy of Sciences. All rights reserved.
PY - 2017/2/14
Y1 - 2017/2/14
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85013001194&partnerID=8YFLogxK
U2 - 10.1073/pnas.1614364114
DO - 10.1073/pnas.1614364114
M3 - مقالة
SN - 0027-8424
VL - 114
SP - E1158-E1167
JO - Proceedings of the National Academy of Sciences - PNAS
JF - Proceedings of the National Academy of Sciences - PNAS
IS - 7
ER -