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Constructing Auxin-Inducible Degron Mutants Using an All-in-One Vector.

Aisha YesbolatovaYuichiro SaitoMasato T Kanemaki
Published in: Pharmaceuticals (Basel, Switzerland) (2020)
Conditional degron-based methods are powerful for studying protein function because a degron-fused protein can be rapidly and efficiently depleted by adding a defined ligand. Auxin-inducible degron (AID) is a popular technology by which a degron-fused protein can be degraded by adding an auxin. However, compared with other technologies such as dTAG and HaloPROTAC, AID is complicated because of its two protein components: OsTIR1 and mAID (degron). To simplify the use of AID in mammalian cells, we constructed bicistronic all-in-one plasmids that express OsTIR1 and a mAID-fused protein using a P2A self-cleavage sequence. To generate a HeLa mutant line for the essential replication factor MCM10, we transfected a CRISPR-knockout plasmid together with a bicistronic plasmid containing mAID-fused MCM10 cDNA. After drug selection and colony isolation, we successfully isolated HeLa mutant lines, in which mAID-MCM10 was depleted by the addition of indole-3-acetic acid, a natural auxin. The bicistronic all-in-one plasmids described in this report are useful for controlling degradation of a transgene-derived protein fused with mAID. These plasmids can be used for the construction of conditional mutants by combining them with a CRISPR-based gene knockout.
Keyphrases
  • escherichia coli
  • protein protein
  • amino acid
  • crispr cas
  • genome wide
  • binding protein
  • gene expression
  • emergency department
  • arabidopsis thaliana
  • wastewater treatment
  • transcription factor
  • drug induced