0000000000499721

AUTHOR

César Díez-villaseñor

0000-0001-6140-9625

showing 2 related works from this author

Cooperation between CRISPR-Cas types enables adaptation in an RNA-targeting system

2020

AbstractCRISPR-Cas immune systems adapt to new threats by acquiring spacers from invading nucleic acids such as phage genomes. However, some CRISPR-Cas loci lack genes necessary for spacer acquisition, despite apparent variation in spacer content between strains. It has been suggested that such loci may use acquisition machinery from co-occurring CRISPR-Cas systems. Here, using a lytic dsDNA phage, we observe spacer acquisition in the native host Flavobacterium columnare that carries an acquisition-deficient subtype VI-B locus and a complete subtype II-C locus. We characterize acquisition events in both loci and show that the RNA-targeting VI-B locus acquires spacers in trans using acquisit…

0303 health sciences030306 microbiologyLocus (genetics)Computational biologyBiologybiology.organism_classificationGenome03 medical and health sciencesLytic cycleFlavobacterium columnareNucleic acidCRISPRTrans-actingGene030304 developmental biology
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Cooperation between Different CRISPR-Cas Types Enables Adaptation in an RNA-Targeting System

2021

CRISPR-Cas systems are immune systems that protect bacteria and archaea against their viruses, bacteriophages. Immunity is achieved through the acquisition of short DNA fragments from the viral invader’s genome.

bacteriophagesanimal diseasesvirusesevoluutiotype VIchemical and pharmacologic phenomenaadaptationFlavobacteriumMicrobiologybakteriofagitbakteeritClustered Regularly Interspaced Short Palindromic Repeatstype II1184 Genetics developmental biology physiologyDNAbiochemical phenomena metabolism and nutritionAdaptation PhysiologicalQR1-502immuunijärjestelmäCRISPRcoevolutionRNA ViralbacteriaRNAspacer acquisitionCRISPR-Cas Systemshorisontaalinen geeninsiirtoGenome BacterialResearch Article
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