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A pathway of targeted autophagy is induced by DNA damage in budding yeast
- Source :
- Proceedings of the National Academy of Sciences, Vol. 114, No 7 (2017) pp. E1158-E1167
- Publication Year :
- 2017
- Publisher :
- Proceedings of the National Academy of Sciences, 2017.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
Programmed cell death
Saccharomyces cerevisiae Proteins
DNA Repair
DNA damage
DNA repair
Saccharomyces cerevisiae
Vesicular Transport Proteins
Autophagy-Related Proteins
Cell Cycle Proteins
Protein Serine-Threonine Kinases
BAG3
03 medical and health sciences
0302 clinical medicine
ddc:590
ddc:570
Autophagy
DNA Breaks, Double-Stranded
DNA, Fungal
Checkpoint Kinase 2
Multidisciplinary
biology
fungi
Intracellular Signaling Peptides and Proteins
biology.organism_classification
Cell biology
body regions
030104 developmental biology
PNAS Plus
Signal transduction
030217 neurology & neurosurgery
DNA Damage
Signal Transduction
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 114
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....49cf444b0432f4a8aa5302943ab1cdb0
- Full Text :
- https://doi.org/10.1073/pnas.1614364114