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DNA interference is controlled by R-loop length in a type I-F1 CRISPR-Cas system.

Donata TuminauskaiteDanguole NorkunaiteMarija FiodorovaiteSarunas TumasInga SongailieneGiedre TamulaitieneTomas Sinkunas
Published in: BMC biology (2020)
We provide a comprehensive characterisation of the DNA interference mechanism in the type I-F1 CRISPR-Cas system, which is different from the type I-E in a few aspects. First, DNA cleavage initiation, which usually happens at the PAM-proximal end in type I-E, is shifted to the PAM-distal end of WT R-loop in the type I-F1. Second, the R-loop length controls on/off switch of DNA interference in the type I-F1, while cleavage initiation is less restricted in the type I-E. These results indicate that DNA interference in type I-F1 systems is governed through a checkpoint provided by the Cascade complex, which verifies the appropriate length for the R-loop.
Keyphrases
  • circulating tumor
  • crispr cas
  • cell free
  • single molecule
  • genome editing
  • transcription factor
  • dna damage
  • circulating tumor cells
  • minimally invasive