Publication:
Binary recombinase systems for high-resolution conditional mutagenesis.

cris.virtual.author-orcid0000-0002-0905-6399
cris.virtualsource.author-orcid79bc2168-817a-44ea-be31-b11af4269ff4
datacite.rightsopen.access
dc.contributor.authorHermann, Mario
dc.contributor.authorStillhard, Patrick
dc.contributor.authorWildner, Hendrik
dc.contributor.authorSeruggia, Davide
dc.contributor.authorKapp, Viktor
dc.contributor.authorSánchez-Iranzo, Héctor
dc.contributor.authorMercader Huber, Nadia Isabel
dc.contributor.authorMontoliu, Lluís
dc.contributor.authorZeilhofer, Hanns Ulrich
dc.contributor.authorPelczar, Pawel
dc.date.accessioned2024-10-24T16:58:37Z
dc.date.available2024-10-24T16:58:37Z
dc.date.issued2014-04
dc.description.abstractConditional mutagenesis using Cre recombinase expressed from tissue specific promoters facilitates analyses of gene function and cell lineage tracing. Here, we describe two novel dual-promoter-driven conditional mutagenesis systems designed for greater accuracy and optimal efficiency of recombination. Co-Driver employs a recombinase cascade of Dre and Dre-respondent Cre, which processes loxP-flanked alleles only when both recombinases are expressed in a predetermined temporal sequence. This unique property makes Co-Driver ideal for sequential lineage tracing studies aimed at unraveling the relationships between cellular precursors and mature cell types. Co-InCre was designed for highly efficient intersectional conditional transgenesis. It relies on highly active trans-splicing inteins and promoters with simultaneous transcriptional activity to reconstitute Cre recombinase from two inactive precursor fragments. By generating native Cre, Co-InCre attains recombination rates that exceed all other binary SSR systems evaluated in this study. Both Co-Driver and Co-InCre significantly extend the utility of existing Cre-responsive alleles.
dc.description.numberOfPages14
dc.description.sponsorshipInstitut für Anatomie
dc.identifier.doi10.7892/boris.79616
dc.identifier.pmid24413561
dc.identifier.publisherDOI10.1093/nar/gkt1361
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/140303
dc.language.isoen
dc.publisherInformation Retrieval Ltd.
dc.relation.ispartofNucleic acids research
dc.relation.issn0305-1048
dc.relation.organizationDCD5A442BCD7E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleBinary recombinase systems for high-resolution conditional mutagenesis.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage3907
oaire.citation.issue6
oaire.citation.startPage3894
oaire.citation.volume42
oairecerif.author.affiliationInstitut für Anatomie
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unibe.description.ispublishedpub
unibe.eprints.legacyId79616
unibe.journal.abbrevTitleNUCLEIC ACIDS RES
unibe.refereedtrue
unibe.subtype.articlejournal

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