| dc.contributor.author | Shmakov, Sergey | |
| dc.contributor.author | Smargon, Aaron Andrew | |
| dc.contributor.author | Scott, David (David Arthur) | |
| dc.contributor.author | Cox, David D. | |
| dc.contributor.author | Pyzocha, Neena | |
| dc.contributor.author | Yan, Winston Xia | |
| dc.contributor.author | Abudayyeh, Omar O. | |
| dc.contributor.author | Gootenberg, Jonathan S | |
| dc.contributor.author | Makarova, Kira S. | |
| dc.contributor.author | Wolf, Yuri I. | |
| dc.contributor.author | Severinov, Konstantin | |
| dc.contributor.author | Zhang, Feng | |
| dc.contributor.author | Koonin, Eugene V. | |
| dc.date.accessioned | 2020-05-20T19:02:48Z | |
| dc.date.available | 2020-05-20T19:02:48Z | |
| dc.date.issued | 2017-01 | |
| dc.identifier.issn | 1740-1526 | |
| dc.identifier.issn | 1740-1534 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/125361 | |
| dc.description.abstract | Class 2 CRISPR-Cas systems are characterized by effector modules that consist of a single multidomain protein, such as Cas9 or Cpf1. We designed a computational pipeline for the discovery of novel class 2 variants and used it to identify six new CRISPR-Cas subtypes. The diverse properties of these new systems provide potential for the development of versatile tools for genome editing and regulation. In this Analysis article, we present a comprehensive census of class 2 types and class 2 subtypes in complete and draft bacterial and archaeal genomes, outline evolutionary scenarios for the independent origin of different class 2 CRISPR-Cas systems from mobile genetic elements, and propose an amended classification and nomenclature of CRISPR-Cas. Keywords:
Bacterial evolution; Bacterial genetics; CRISPR-Cas systems | en_US |
| dc.description.sponsorship | US National Institute of Mental Health (Grant 5DP1-MH100706) | en_US |
| dc.description.sponsorship | US National Institute of Mental Health (Grant 1R01-MH110049) | en_US |
| dc.language.iso | en | |
| dc.publisher | Springer Science and Business Media LLC | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1038/nrmicro.2016.184 | en_US |
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
| dc.source | PMC | en_US |
| dc.title | Diversity and evolution of class 2 CRISPR–Cas systems | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Shmakov, Sergey et al. "Diversity and evolution of class 2 CRISPR–Cas systems." Nature Reviews Microbiology 15, 3 (March 2017): 169–182 | en_US |
| dc.contributor.department | Broad Institute of MIT and Harvard | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
| dc.contributor.department | Harvard University--MIT Division of Health Sciences and Technology | en_US |
| dc.contributor.department | McGovern Institute for Brain Research at MIT | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
| dc.relation.journal | Nature Reviews Microbiology | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2019-10-08T12:18:08Z | |
| dspace.date.submission | 2019-10-08T12:18:11Z | |
| mit.journal.volume | 15 | en_US |
| mit.journal.issue | 3 | en_US |
| mit.metadata.status | Complete | |