Binary recombinase systems for high-resolution conditional mutagenesis.
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BORIS DOI
Date of Publication
April 2014
Publication Type
Article
Division/Institute
Author
Hermann, Mario | |
Stillhard, Patrick | |
Wildner, Hendrik | |
Seruggia, Davide | |
Kapp, Viktor | |
Sánchez-Iranzo, Héctor | |
Montoliu, Lluís | |
Zeilhofer, Hanns Ulrich | |
Pelczar, Pawel |
Subject(s)
Series
Nucleic acids research
ISSN or ISBN (if monograph)
0305-1048
Publisher
Information Retrieval Ltd.
Language
English
Publisher DOI
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.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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3894.full.pdf | text | Adobe PDF | 10.85 MB | Attribution-NonCommercial (CC BY-NC 4.0) | published |