| Literature DB >> 32023459 |
Michael M Dubreuil1, David W Morgens2, Kanji Okumoto3, Masanori Honsho4, Kévin Contrepois2, Brittany Lee-McMullen2, Gavin McAllister Traber2, Ria S Sood2, Scott J Dixon5, Michael P Snyder2, Yukio Fujiki6, Michael C Bassik7.
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.Entities:
Keywords: CRISPR; catalase; genome-wide screen; oxidative stress; pentose phosphate pathway; peroxisomal import pathway; phosphogluconate dehydrogenase; reactive oxygen species; shRNA
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Year: 2020 PMID: 32023459 PMCID: PMC7184925 DOI: 10.1016/j.celrep.2020.01.013
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423