Publication:
A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation

dc.contributor.authorLucas-Elio, Patricia
dc.contributor.authorMolina-Quintero, Luisa Raquel
dc.contributor.authorXu, Hengyi
dc.contributor.authorSánchez-Amat, Antonio
dc.contributor.departmentGenética y Microbiología
dc.date.accessioned2025-01-14T13:16:17Z
dc.date.available2025-01-14T13:16:17Z
dc.date.issued2021-10-18
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.abstractCRISPR-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.formatapplication/pdfes
dc.format.extent13es
dc.identifier.citationScientific Reports (2021) 11:20564
dc.identifier.doihttps://doi.org/10.1038/s41598-021-99740-9
dc.identifier.issnElectronic: 2045-2322
dc.identifier.urihttp://hdl.handle.net/10201/148423
dc.languageenges
dc.publisherNature Researches
dc.relationDiversidad 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.relation.publisherversionhttps://www.nature.com/articles/s41598-021-99740-9
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMarinomonas mediterraneaes
dc.subjectCRISPR-Cases
dc.subjectBacteriofagoes
dc.subjectRegulaciónes
dc.subject.otherCDU::5 - Ciencias puras y naturales::57 - Biología::579 - Microbiologíaes
dc.titleA histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulationes
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
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