TY - JOUR
T1 - CRISPR-Cas adaptation
T2 - Insights into the mechanism of action
AU - Amitai, Gil
AU - Sorek, Rotem
N1 - Israel Science Foundation [1303/ 12]; Israeli Centers of Research Excellence (I-CORE) [1796/ 12]; European Research Council (ERC) [260432]; Human Frontier Science Program (HFSP) [RGP0011/2013]; Abisch-Frenkel foundation; Pasteur-Weizmann council; Institut Merieux; Leona M. and Harry B. Helmsley Charitable Trust; Minerva Foundation; Deutsche Forschungsgemeinschaft (a Deutsch-Israelische Projektkooperation (DIP) grant) The authors thank P. Fineran for discussions on primed acquisition. R.S. was supported, in part, by the Israel Science Foundation (personal grant 1303/ 12 and Israeli Centers of Research Excellence (I-CORE) grant 1796/ 12), the European Research Council (ERC; Starting Grant 260432), the Human Frontier Science Program (HFSP; grant RGP0011/2013), the Abisch-Frenkel foundation, the Pasteur-Weizmann council, the Institut Merieux, the Leona M. and Harry B. Helmsley Charitable Trust, the Minerva Foundation and the Deutsche Forschungsgemeinschaft (a Deutsch-Israelische Projektkooperation (DIP) grant).
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Since the first demonstration that CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against phages and plasmids, numerous studies have yielded key insights into the molecular mechanisms governing how these systems attack and degrade foreign DNA. However, the molecular mechanisms underlying the adaptation stage, in which new immunological memory is formed, have until recently represented a major unresolved question. In this Progress article, we discuss recent discoveries that have shown both how foreign DNA is identified by the CRISPR-Cas adaptation machinery and the molecular basis for its integration into the chromosome to form an immunological memory. Furthermore, we describe the roles of each of the specific CRISPR-Cas components that are involved in memory formation, and consider current models for their evolutionary origin.
AB - Since the first demonstration that CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against phages and plasmids, numerous studies have yielded key insights into the molecular mechanisms governing how these systems attack and degrade foreign DNA. However, the molecular mechanisms underlying the adaptation stage, in which new immunological memory is formed, have until recently represented a major unresolved question. In this Progress article, we discuss recent discoveries that have shown both how foreign DNA is identified by the CRISPR-Cas adaptation machinery and the molecular basis for its integration into the chromosome to form an immunological memory. Furthermore, we describe the roles of each of the specific CRISPR-Cas components that are involved in memory formation, and consider current models for their evolutionary origin.
UR - http://www.scopus.com/inward/record.url?scp=84954537942&partnerID=8YFLogxK
U2 - 10.1038/nrmicro.2015.14
DO - 10.1038/nrmicro.2015.14
M3 - مقالة
SN - 1740-1526
VL - 14
SP - 67
EP - 76
JO - Nature Reviews Microbiology
JF - Nature Reviews Microbiology
IS - 2
ER -