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http://purl.uniprot.org/citations/34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34810254http://www.w3.org/2000/01/rdf-schema#comment"Enzymes that produce second messengers are highly regulated. Revealing the mechanisms underlying such regulation is critical to understanding both how cells achieve specific signaling outcomes and return to homeostasis following a particular stimulus. Pooled genome-wide CRISPR screens are powerful unbiased approaches to elucidate regulatory networks, their principal limitation being the choice of phenotype selection. Here, we merge advances in bioorthogonal fluorescent labeling and CRISPR screening technologies to discover regulators of phospholipase D (PLD) signaling, which generates the potent lipid second messenger phosphatidic acid. Our results reveal glycogen synthase kinase 3 as a positive regulator of protein kinase C and PLD signaling. More generally, this work demonstrates how bioorthogonal, activity-based fluorescent tagging can expand the power of CRISPR screening to uncover mechanisms regulating specific enzyme-driven signaling pathways in mammalian cells."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.org/dc/terms/identifier"doi:10.1073/pnas.2025265118"xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/author"Huang S."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/author"Baskin J.M."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/author"Tei R."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/author"Bumpus T.W."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/name"Proc Natl Acad Sci U S A"xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/pages"e2025265118"xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/title"Click chemistry-enabled CRISPR screening reveals GSK3 as a regulator of PLD signaling."xsd:string
http://purl.uniprot.org/citations/34810254http://purl.uniprot.org/core/volume"118"xsd:string
http://purl.uniprot.org/citations/34810254http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34810254
http://purl.uniprot.org/citations/34810254http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34810254
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http://purl.uniprot.org/uniprot/#_P49840-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
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http://purl.uniprot.org/uniprot/#_P17252-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
http://purl.uniprot.org/uniprot/#_Q2TSD3-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
http://purl.uniprot.org/uniprot/#_Q13393-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
http://purl.uniprot.org/uniprot/#_Q59EA4-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
http://purl.uniprot.org/uniprot/#_Q59FI5-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254
http://purl.uniprot.org/uniprot/#_Q68D16-mappedCitation-34810254http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34810254