| Literature DB >> 30993331 |
Kira S Makarova1, Svetlana Karamycheva1, Shiraz A Shah2, Gisle Vestergaard3, Roger A Garrett2, Eugene V Koonin1.
Abstract
Screening of genomic and metagenomic databases for new variants of CRISPR-Cas systems increasingly results in the discovery of derived variants that do not seem to possess the interference capacity and are implicated in functions distinct from adaptive immunity. We describe an extremely derived putative class 1 CRISPR-Cas system that is present in many Halobacteria and consists of distant homologs of the Cas5 and Cas7 protein along with an uncharacterized conserved protein and various nucleases. We hypothesize that, although this system lacks typical CRISPR effectors or a CRISPR array, it functions as a RNA-dependent defense mechanism that, unlike other derived CRISPR-Cas, utilizes alternative nucleases to cleave invader genomes. Published by Oxford University Press on behalf of FEMS 2019.Entities:
Keywords: CRISPR-Cas systems; Cas7, Cas5; Halobacteria; defense systems; nuclease
Mesh:
Substances:
Year: 2019 PMID: 30993331 PMCID: PMC6702361 DOI: 10.1093/femsle/fnz079
Source DB: PubMed Journal: FEMS Microbiol Lett ISSN: 0378-1097 Impact factor: 2.742