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An updated evolutionary classification of CRISPR-Cas systems including rare variants

  • Kira S Makarova
  • , Sergey A Shmakov
  • , Yuri I Wolf
  • , Pascal Mutz
  • , Han Altae-Tran
  • , Chase L Beisel
  • , Stan J J Brouns
  • , Emmanuelle Charpentier
  • , David Cheng
  • , Jennifer Doudna
  • , Daniel H Haft
  • , Philippe Horvath
  • , Sylvain Moineau
  • , Francisco J M Mojica
  • , Patrick Pausch
  • , Rafael Pinilla-Redondo
  • , Shiraz A Shah
  • , Virginijus Siksnys
  • , Michael P Terns
  • , Jesse Tordoff
  • Česlovas Venclovas, Malcolm F White, Alexander F Yakunin, Feng Zhang, Roger A Garrett, Rolf Backofen, John van der Oost, Rodolphe Barrangou, Eugene V Koonin
  • National Institutes of Health
  • University of Washington
  • Helmholtz Institute for RNA-based Infection Research (HIRI)
  • Delft University of Technology
  • Humboldt-University, Berlin
  • Arbor Biotechnologies
  • University of California
  • Dangé-Saint-Romain
  • Universite Laval
  • Universidad de Alicante
  • Vilnius University
  • University of Copenhagen
  • University of Georgia
  • University of St. Andrews
  • Broad Institute of MIT and Harvard
  • Copenhagen University Hospital
  • University of Freiburg
  • Wageningen University
  • North Carolina State University

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

Crynodeb

The known diversity of CRISPR-Cas systems continues to expand. To encompass new discoveries, here we present an updated evolutionary classification of CRISPR-Cas systems. The updated CRISPR-Cas classification includes 2 classes, 7 types and 46 subtypes, compared with the 6 types and 33 subtypes in our previous survey 5 years ago. In addition, a classification of the cyclic oligoadenylate-dependent signalling pathway in type III systems is presented. We also discuss recently characterized alternative CRISPR-Cas functionalities, notably, type IV variants that cleave the target DNA and type V variants that inhibit the target replication without cleavage. Analysis of the abundance of CRISPR-Cas variants in genomes and metagenomes shows that the previously defined systems are relatively common, whereas the more recently characterized variants are comparatively rare. These low abundance variants comprise the long tail of the CRISPR-Cas distribution in prokaryotes and their viruses, and remain to be characterized experimentally.

Iaith wreiddiolSaesneg
Tudalennau (o-i)3346-3361
Nifer y tudalennau16
CyfnodolynNature Microbiology
Cyfrol10
Rhif cyhoeddi12
Dyddiad ar-lein cynnar6 Tach 2025
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 6 Tach 2025

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