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  3. Binary recombinase systems for high-resolution conditional mutagenesis.
 

Binary recombinase systems for high-resolution conditional mutagenesis.

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BORIS DOI
10.7892/boris.79616
Date of Publication
April 2014
Publication Type
Article
Division/Institute

Institut für Anatomie...

Author
Hermann, Mario
Stillhard, Patrick
Wildner, Hendrik
Seruggia, Davide
Kapp, Viktor
Sánchez-Iranzo, Héctor
Mercader Huber, Nadia Isabelorcid-logo
Institut für Anatomie
Montoliu, Lluís
Zeilhofer, Hanns Ulrich
Pelczar, Pawel
Subject(s)

600 - Technology::610...

Series
Nucleic acids research
ISSN or ISBN (if monograph)
0305-1048
Publisher
Information Retrieval Ltd.
Language
English
Publisher DOI
10.1093/nar/gkt1361
PubMed ID
24413561
Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/140303
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
3894.full.pdftextAdobe PDF10.85 MBAttribution-NonCommercial (CC BY-NC 4.0)publishedOpen
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