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A one-step tRNA-CRISPR system for genome-wide genetic interaction mapping in mammalian cells.

Yulei ZhaoKathrin TyrishkinCalvin SjaardaPrem KhanalJeff StaffordMichael J RauhXudong LiuTomas BabakXiaolong Yang
Published in: Scientific reports (2019)
Mapping genetic interactions in mammalian cells is limited due to technical obstacles. Here we describe a method called TCGI (tRNA-CRISPR for genetic interactions) to generate a high-efficient, barcode-free and scalable pairwise CRISPR libraries in mammalian cells for identifying genetic interactions. We have generated a genome- wide library to identify genes genetically interacting with TAZ in cell viability regulation. Validation of candidate synergistic genes reveals the screening accuracy of 85% and TAZ-MCL1 is characterized as combinational drug targets for non-small cell lung cancer treatments. TCGI has dramatically improved the current methods for mapping genetic interactions and screening drug targets for combinational therapies.
Keyphrases
  • genome wide
  • dna methylation
  • copy number
  • high resolution
  • gene expression
  • high density
  • crispr cas
  • drug induced
  • transcription factor