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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Lucas-Elio, Patricia | - |
dc.contributor.author | Molina-Quintero, Luisa Raquel | - |
dc.contributor.author | Xu, Hengyi | - |
dc.contributor.author | Sánchez-Amat, Antonio | - |
dc.date.accessioned | 2025-01-14T13:16:17Z | - |
dc.date.available | 2025-01-14T13:16:17Z | - |
dc.date.issued | 2021-10-18 | - |
dc.identifier.citation | Scientific Reports (2021) 11:20564 | es |
dc.identifier.issn | Electronic: 2045-2322 | - |
dc.identifier.uri | http://hdl.handle.net/10201/148423 | - |
dc.description | © The Author(s) 2021. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by/4.0/. This document is the Published version of a Published Work that appeared in final form in Scientific Reports. To access the final edited and published work see https://doi.org/10.1038/s41598-021-99740-9 | - |
dc.description.abstract | CRISPR-Cas systems are used by many prokaryotes to defend against invading genetic elements. In many cases, more than one CRISPR-Cas system co-exist in the same cell. Marinomonas mediterranea MMB-1 possesses two CRISPR-Cas systems, of type I-F and III-B respectively, which collaborate in phage resistance raising questions on how their expression is regulated. This study shows that the expression of both systems is controlled by the histidine kinase PpoS and a response regulator, PpoR, identified and cloned in this study. These proteins show similarity to the global regulators BarA/UvrY. In addition, homologues to the sRNAs CsrB and CsrC and the gene coding for the post-transcriptional repressor CsrA have been also identified indicating the conservation of the elements of the BarA/UvrY regulatory cascade in M. mediterranea. RNA-Seq analyses have revealed that all these genetics elements are regulated by PpoS/R supporting their participation in the regulatory cascade. The regulation by PpoS and PpoR of the CRISPR-Cas systems plays a role in phage defense since mutants in these proteins show an increase in phage sensitivity. | es |
dc.format | application/pdf | es |
dc.format.extent | 13 | es |
dc.language | eng | es |
dc.publisher | Nature Research | es |
dc.relation | Diversidad funcional de sistemas CRISPR-Cas. Papel de los sistemas con RT-Cas1 en la defensa frente a fagos. Ministerio de Economía, Industria y Competitividad (BFU2017-85464) Identificación de elementos genéticos infectivos diana de sistemas CRISPR-Cas. Fundación Séneca, Comunidad Autónoma de la Región de Murcia (20883/PI/18). The analysis of RNAseq data by Hengyi Xu was supported by NIH grants R01 GM37949 and R35 GM136216 to Alan M. Lambowitz. | es |
dc.rights | info:eu-repo/semantics/openAccess | es |
dc.rights | Atribución 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | Marinomonas mediterranea | es |
dc.subject | CRISPR-Cas | es |
dc.subject | Bacteriofago | es |
dc.subject | Regulación | es |
dc.subject.other | CDU::5 - Ciencias puras y naturales::57 - Biología::579 - Microbiología | es |
dc.title | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation | es |
dc.type | info:eu-repo/semantics/article | es |
dc.relation.publisherversion | https://www.nature.com/articles/s41598-021-99740-9 | - |
dc.identifier.doi | https://doi.org/10.1038/s41598-021-99740-9 | - |
dc.contributor.department | Genética y Microbiología | - |
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