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Evolutionary classification of CRISPR-Cas systems: a burst of class 2 and derived variants

  • Kira S Makarova
  • , Yuri I Wolf
  • , Jaime Iranzo
  • , Sergey A Shmakov
  • , Omer S Alkhnbashi
  • , Stan J J Brouns
  • , Emmanuelle Charpentier
  • , David Cheng
  • , Daniel H Haft
  • , Philippe Horvath
  • , Sylvain Moineau
  • , Francisco J M Mojica
  • , David Scott
  • , Shiraz A Shah
  • , Virginijus Siksnys
  • , Michael P Terns
  • , Česlovas Venclovas
  • , Malcolm F White
  • , Alexander F Yakunin
  • , Winston Yan
  • Feng Zhang, Roger A Garrett, Rolf Backofen, John van der Oost, Rodolphe Barrangou, Eugene V Koonin
  • National Center for Biotechnology Information
  • University of Freiberg
  • Delft University of Technology
  • Humboldt-University, Berlin
  • Arbor Biotechnologies
  • DuPont Nutrition and Health
  • Félix d'Hérelle Reference Center for Bacterial Viruses
  • Departamento de Fisiología
  • University of Copenhagen
  • Vilnius University
  • University of Georgia
  • University of St. Andrews
  • University of Toronto
  • Broad Institute of MIT and Harvard
  • Copenhagen University Hospital
  • Wageningen University
  • North Carolina State University

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygl adolyguadolygiad gan gymheiriaid

Crynodeb

The number and diversity of known CRISPR-Cas systems have substantially increased in recent years. Here, we provide an updated evolutionary classification of CRISPR-Cas systems and cas genes, with an emphasis on the major developments that have occurred since the publication of the latest classification, in 2015. The new classification includes 2 classes, 6 types and 33 subtypes, compared with 5 types and 16 subtypes in 2015. A key development is the ongoing discovery of multiple, novel class 2 CRISPR-Cas systems, which now include 3 types and 17 subtypes. A second major novelty is the discovery of numerous derived CRISPR-Cas variants, often associated with mobile genetic elements that lack the nucleases required for interference. Some of these variants are involved in RNA-guided transposition, whereas others are predicted to perform functions distinct from adaptive immunity that remain to be characterized experimentally. The third highlight is the discovery of numerous families of ancillary CRISPR-linked genes, often implicated in signal transduction. Together, these findings substantially clarify the functional diversity and evolutionary history of CRISPR-Cas.

Iaith wreiddiolSaesneg
Tudalennau (o-i)67-83
Nifer y tudalennau17
CyfnodolynNature reviews. Microbiology
Cyfrol18
Rhif cyhoeddi2
Dyddiad ar-lein cynnar19 Rhag 2019
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - Chwef 2020
Cyhoeddwyd yn allanolIe

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