DNA targeting by Clostridium cellulolyticum CRISPR-Cas9 Type II-C system

Nucleic Acids Res. 2020 Feb 28;48(4):2026-2034. doi: 10.1093/nar/gkz1225.

Abstract

Type II CRISPR-Cas9 RNA-guided nucleases are widely used for genome engineering. Type II-A SpCas9 protein from Streptococcus pyogenes is the most investigated and highly used enzyme of its class. Nevertheless, it has some drawbacks, including a relatively big size, imperfect specificity and restriction to DNA targets flanked by an NGG PAM sequence. Cas9 orthologs from other bacterial species may provide a rich and largely untapped source of biochemical diversity, which can help to overcome the limitations of SpCas9. Here, we characterize CcCas9, a Type II-C CRISPR nuclease from Clostridium cellulolyticum H10. We show that CcCas9 is an active endonuclease of comparatively small size that recognizes a novel two-nucleotide PAM sequence. The CcCas9 can potentially broaden the existing scope of biotechnological applications of Cas9 nucleases and may be particularly advantageous for genome editing of C. cellulolyticum H10, a bacterium considered to be a promising biofuel producer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CRISPR-Associated Protein 9 / chemistry*
  • CRISPR-Associated Protein 9 / genetics
  • CRISPR-Cas Systems / genetics*
  • Clostridium cellulolyticum / enzymology*
  • Crystallography, X-Ray
  • DNA / chemistry*
  • DNA / genetics
  • Gene Editing
  • Mutation
  • Nucleotide Motifs / genetics
  • RNA, Guide, CRISPR-Cas Systems / genetics
  • Streptococcus pyogenes / enzymology
  • Substrate Specificity

Substances

  • RNA, Guide, CRISPR-Cas Systems
  • DNA
  • CRISPR-Associated Protein 9