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Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway.
- Source :
-
Cell reports [Cell Rep] 2020 Feb 04; Vol. 30 (5), pp. 1417-1433.e7. - Publication Year :
- 2020
-
Abstract
- Reactive oxygen species (ROS) play critical roles in metabolism and disease, yet a comprehensive analysis of the cellular response to oxidative stress is lacking. To systematically identify regulators of oxidative stress, we conducted genome-wide Cas9/CRISPR and shRNA screens. This revealed a detailed picture of diverse pathways that control oxidative stress response, ranging from the TCA cycle and DNA repair machineries to iron transport, trafficking, and metabolism. Paradoxically, disrupting the pentose phosphate pathway (PPP) at the level of phosphogluconate dehydrogenase (PGD) protects cells against ROS. This dramatically alters metabolites in the PPP, consistent with rewiring of upper glycolysis to promote antioxidant production. In addition, disruption of peroxisomal import unexpectedly increases resistance to oxidative stress by altering the localization of catalase. Together, these studies provide insights into the roles of peroxisomal matrix import and the PPP in redox biology and represent a rich resource for understanding the cellular response to oxidative stress.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.<br /> (Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Subjects :
- CRISPR-Cas Systems
Catalase metabolism
Cytoprotection
Cytosol metabolism
Genome, Human
Glucose metabolism
Glycolysis
HeLa Cells
Humans
K562 Cells
Phosphogluconate Dehydrogenase
Protein Transport
RNA, Small Interfering metabolism
Reactive Oxygen Species metabolism
Oxidative Stress
Pentose Phosphate Pathway
Peroxisomes metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 30
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 32023459
- Full Text :
- https://doi.org/10.1016/j.celrep.2020.01.013