Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-775
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dc.contributor.authorScheuermann, Barbara-
dc.contributor.authorDiem, Tanja-
dc.contributor.authorIvics, Zoltán-
dc.contributor.authorAndrade, Miguel-
dc.date.accessioned2019-04-23T09:26:47Z-
dc.date.available2019-04-23T11:26:47Z-
dc.date.issued2019-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/777-
dc.description.abstractSleeping Beauty (SB) is a synthetic Tc1/mariner transposon that is widely used for genetic engineering in vertebrates, including humans. Its sequence was derived from a consensus of sequences found in fish species including the Atlantic salmon (Salmo salar). One of the functional components of SB, the transposase enzyme, has been subject to extensive mutagenesis yielding hyperactive protein variants for advanced applications. The second functional component, the transposon inverted terminal repeats (ITRs), has so far not been extensively modified, mainly due to a lack of natural sequence information. Importantly, as genome sequences become available, they can provide a rich source of information for a refined molecular definition of the functional components of these transposons. Here we have mined the Salmo salar genome for a comprehensive set of transposon sequences that were used to build a refined consensus sequence. We synthetically produced the new consensus ITR sequences and used them to build a new transposon, the performance of which has been tested in cell-based transposition assays. The consensus sequence did not support enhanced transposition, suggesting alternative mechanisms responsible for the preferential amplification of these sequence variants in the salmon genome.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin-
dc.language.isoeng-
dc.rightsCC BYde_DE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.titleEvolution-guided evaluation of the inverted terminal repeats of the synthetic transposon Sleeping Beautyen_GB
dc.typeZeitschriftenaufsatzde_DE
dc.identifier.doihttp://doi.org/10.25358/openscience-775-
jgu.type.dinitypearticle-
jgu.type.versionPublished versionen_GB
jgu.type.resourceText-
jgu.organisation.departmentFB 10 Biologie-
jgu.organisation.number7970-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleScientific reports-
jgu.journal.volume9-
jgu.pages.alternativeArt. 1171-
jgu.publisher.year2019-
jgu.publisher.nameMacmillan Publishers Limited, part of Springer Nature-
jgu.publisher.placeLondon-
jgu.publisher.urihttp://dx.doi.org/10.1038/s41598-018-38061-w-
jgu.publisher.issn2045-2322-
jgu.notes.publicAndrade, Miguel veröffentlicht unter: Andrade-Navarro, Miguel A.de_DE
jgu.organisation.placeMainz-
jgu.subject.ddccode570-
opus.date.accessioned2019-04-23T09:26:47Z-
opus.date.modified2019-05-06T10:37:36Z-
opus.date.available2019-04-23T11:26:47-
opus.subject.dfgcode00-000-
opus.organisation.stringFB 10: Biologie: Institut für Organismische und Molekulare Evolutionsbiologiede_DE
opus.identifier.opusid59042-
opus.institute.number1011-
opus.metadataonlyfalse-
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_GB
opus.affiliatedAndrade, Miguel-
jgu.publisher.doi10.1038/s41598-018-38061-w
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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