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Cell Rep ; 30(5): 1417-1433.e7, 2020 02 04.
Artigo em Inglês | MEDLINE | ID: mdl-32023459

RESUMO

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.


Assuntos
Estresse Oxidativo , Via de Pentose Fosfato , Peroxissomos/metabolismo , Sistemas CRISPR-Cas , Catalase/metabolismo , Citoproteção , Citosol/metabolismo , Genoma Humano , Glucose/metabolismo , Glicólise , Células HeLa , Humanos , Células K562 , Fosfogluconato Desidrogenase , Transporte Proteico , RNA Interferente Pequeno/metabolismo , Espécies Reativas de Oxigênio/metabolismo
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