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dc.contributor.authorSidik, Saima M.
dc.contributor.authorHackett, Caroline G.
dc.contributor.authorTran, Fanny
dc.contributor.authorWestwood, Nicholas J.
dc.contributor.authorLourido, Sebastian
dc.date.accessioned2014-08-11T16:01:01Z
dc.date.available2014-08-11T16:01:01Z
dc.date.issued2014-06-27
dc.identifier139613000
dc.identifier5f102462-c325-4f8f-81a2-8a9f6b1d5731
dc.identifier000338512200032
dc.identifier84903544109
dc.identifier000338512200032
dc.identifier.citationSidik , S M , Hackett , C G , Tran , F , Westwood , N J & Lourido , S 2014 , ' Efficient genome engineering of Toxoplasma gondii using CRISPR/Cas9 ' , PLoS One , vol. 9 , no. 6 , e100450 . https://doi.org/10.1371/journal.pone.0100450en
dc.identifier.issn1932-6203
dc.identifier.otherORCID: /0000-0003-0630-0138/work/56424171
dc.identifier.urihttps://hdl.handle.net/10023/5110
dc.descriptionThis work was supported in part by NIH grant 1DP5OD017892 to S.Len
dc.description.abstractToxoplasma gondii is a parasite of humans and animals, and a model for other apicomplexans including Plasmodium spp., the causative agents of malaria. Despite many advances, manipulating the T. gondii genome remains labor intensive, and is often restricted to lab-adapted strains or lines carrying mutations that enable selection. Here, we use the RNA-guided Cas9 nuclease to efficiently generate knockouts without selection, and to introduce point mutations and epitope tags into the T. gondii genome. These methods will streamline the functional analysis of parasite genes and enable high-throughput engineering of their genomes.
dc.format.extent8
dc.format.extent1552210
dc.language.isoeng
dc.relation.ispartofPLoS Oneen
dc.subjectInvasionen
dc.subjectSystemsen
dc.subjectMarkeren
dc.subjectGenesen
dc.subjectQD Chemistryen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccQDen
dc.titleEfficient genome engineering of Toxoplasma gondii using CRISPR/Cas9en
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1371/journal.pone.0100450
dc.description.statusPeer revieweden


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