Publication: Binary recombinase systems for high-resolution conditional mutagenesis.
cris.virtual.author-orcid | 0000-0002-0905-6399 | |
cris.virtualsource.author-orcid | 79bc2168-817a-44ea-be31-b11af4269ff4 | |
datacite.rights | open.access | |
dc.contributor.author | Hermann, Mario | |
dc.contributor.author | Stillhard, Patrick | |
dc.contributor.author | Wildner, Hendrik | |
dc.contributor.author | Seruggia, Davide | |
dc.contributor.author | Kapp, Viktor | |
dc.contributor.author | Sánchez-Iranzo, Héctor | |
dc.contributor.author | Mercader Huber, Nadia Isabel | |
dc.contributor.author | Montoliu, Lluís | |
dc.contributor.author | Zeilhofer, Hanns Ulrich | |
dc.contributor.author | Pelczar, Pawel | |
dc.date.accessioned | 2024-10-24T16:58:37Z | |
dc.date.available | 2024-10-24T16:58:37Z | |
dc.date.issued | 2014-04 | |
dc.description.abstract | Conditional 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.numberOfPages | 14 | |
dc.description.sponsorship | Institut für Anatomie | |
dc.identifier.doi | 10.7892/boris.79616 | |
dc.identifier.pmid | 24413561 | |
dc.identifier.publisherDOI | 10.1093/nar/gkt1361 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/140303 | |
dc.language.iso | en | |
dc.publisher | Information Retrieval Ltd. | |
dc.relation.ispartof | Nucleic acids research | |
dc.relation.issn | 0305-1048 | |
dc.relation.organization | DCD5A442BCD7E17DE0405C82790C4DE2 | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Binary recombinase systems for high-resolution conditional mutagenesis. | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.endPage | 3907 | |
oaire.citation.issue | 6 | |
oaire.citation.startPage | 3894 | |
oaire.citation.volume | 42 | |
oairecerif.author.affiliation | Institut für Anatomie | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 79616 | |
unibe.journal.abbrevTitle | NUCLEIC ACIDS RES | |
unibe.refereed | true | |
unibe.subtype.article | journal |
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