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- W4311036075 abstract "Abstract Loss-of-function and gain-of-function genetic perturbations provide valuable insights into gene function. In Drosophila cells, while genome-wide loss-of-function screens have been extensively used to reveal mechanisms of a variety of biological processes, approaches for performing genome-wide gain-of-function screens are still lacking. Here, we describe a pooled CRISPR activation (CRISPRa) screening platform in Drosophila cells and apply this method to both focused and genome-wide screens to identify rapamycin resistance genes. The screens identified three genes as novel rapamycin resistance genes: a member of SLC16 family of monocarboxylate transporters ( CG8468) , a member of the lipocalin protein family ( CG5399 ), and a zinc finger C2H2 transcription factor ( CG9932 ). Mechanistically, we demonstrate that CG5399 overexpression activates the RTK-Akt-mTOR signaling pathway and that activation of InR by CG5399 requires cholesterol and clathrin-coated pits at the cell membrane. This study establishes a novel platform for functional genetic studies in Drosophila cells." @default.
- W4311036075 created "2022-12-22" @default.
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- W4311036075 date "2022-12-10" @default.
- W4311036075 modified "2023-10-15" @default.
- W4311036075 title "Pooled genome-wide CRISPR activation screening for rapamycin resistance genes in<i>Drosophila</i>cells" @default.
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- W4311036075 doi "https://doi.org/10.1101/2022.12.09.519790" @default.
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