Publication: Type III CRISPR-Cas systems can provide redundancy to counteract viral escape from type I systems
| dc.contributor.author | Silas, Sukrit | |
| dc.contributor.author | Elío Lucas, Patrícia | |
| dc.contributor.author | Jackson, Simon A. | |
| dc.contributor.author | Aroca Crevillén, Alejandra | |
| dc.contributor.author | Hansen, Loren L. | |
| dc.contributor.author | Fineran, Peter C. | |
| dc.contributor.author | Fire, Andrew Z. | |
| dc.contributor.author | Sánchez Amat, Antonio | |
| dc.contributor.department | Genética y Microbiología | |
| dc.date.accessioned | 2026-01-12T13:00:57Z | |
| dc.date.available | 2026-01-12T13:00:57Z | |
| dc.date.copyright | © Silas et al. 2017 | |
| dc.date.issued | 2017-08-17 | |
| dc.description.abstract | CRISPR-Cas-mediated defense utilizes information stored as spacers in CRISPR arrays to defend against genetic invaders. We define the mode of target interference and role in antiviral defense for two CRISPR-Cas systems in Marinomonas mediterranea. One system (type I-F) targets DNA. A second system (type III-B) is broadly capable of acquiring spacers in either orientation from RNA and DNA, and exhibits transcription-dependent DNA interference. Examining resistance to phages isolated from Mediterranean seagrass meadows, we found that the type III-B machinery co- opts type I-F CRISPR-RNAs. Sequencing and infectivity assessments of related bacterial and phage strains suggests an ‘arms race’ in which phage escape from the type I-F system can be overcome through use of type I-F spacers by a horizontally-acquired type III-B system. We propose that the phage-host arms race can drive selection for horizontal uptake and maintenance of promiscuous type III interference modules that supplement existing host type I CRISPR-Cas systems. | |
| dc.format | application/pdf | |
| dc.format.extent | 27 | |
| dc.identifier.citation | eLife, 2017, Vol. 6 : e27601 | |
| dc.identifier.doi | https://doi.org/10.7554/eLife.27601.001 | |
| dc.identifier.eissn | 2050-084X | |
| dc.identifier.uri | http://hdl.handle.net/10201/185731 | |
| dc.language | eng | |
| dc.publisher | eLife Sciences Publications | |
| dc.relation | Nacional: PID2021- 124464NB-I00 | |
| dc.relation.publisherversion | https://elifesciences.org/articles/27601 | |
| dc.rights | Attribution 4.0 International | * |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject.ods | No relacionado con ningún objetivo de desarrollo sostenible | |
| dc.title | Type III CRISPR-Cas systems can provide redundancy to counteract viral escape from type I systems | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dspace.entity.type | Publication | es |
| relation.isAuthorOfPublication | 66095fe4-223f-4dbc-9b73-7cade64d2e20 | |
| relation.isAuthorOfPublication | 15331c24-15e1-4518-824f-57238c36ed42 | |
| relation.isAuthorOfPublication.latestForDiscovery | 66095fe4-223f-4dbc-9b73-7cade64d2e20 |
Collections
Este ítem está sujeto a una licencia Creative Commons. http://creativecommons.org/licenses/by/4.0/