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Binary recombinase systems for high-resolution conditional mutagenesis

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 recombinatio...

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Autores principales: Hermann, Mario, Stillhard, Patrick, Wildner, Hendrik, Seruggia, Davide, Kapp, Viktor, Sánchez-Iranzo, Héctor, Mercader, Nadia, Montoliu, Lluís, Zeilhofer, Hanns Ulrich, Pelczar, Pawel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973285/
https://www.ncbi.nlm.nih.gov/pubmed/24413561
http://dx.doi.org/10.1093/nar/gkt1361
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author Hermann, Mario
Stillhard, Patrick
Wildner, Hendrik
Seruggia, Davide
Kapp, Viktor
Sánchez-Iranzo, Héctor
Mercader, Nadia
Montoliu, Lluís
Zeilhofer, Hanns Ulrich
Pelczar, Pawel
author_facet Hermann, Mario
Stillhard, Patrick
Wildner, Hendrik
Seruggia, Davide
Kapp, Viktor
Sánchez-Iranzo, Héctor
Mercader, Nadia
Montoliu, Lluís
Zeilhofer, Hanns Ulrich
Pelczar, Pawel
author_sort Hermann, Mario
collection PubMed
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.
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spelling pubmed-39732852014-04-04 Binary recombinase systems for high-resolution conditional mutagenesis Hermann, Mario Stillhard, Patrick Wildner, Hendrik Seruggia, Davide Kapp, Viktor Sánchez-Iranzo, Héctor Mercader, Nadia Montoliu, Lluís Zeilhofer, Hanns Ulrich Pelczar, Pawel Nucleic Acids Res Nucleic Acid Enzymes 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. Oxford University Press 2014-04 2014-01-09 /pmc/articles/PMC3973285/ /pubmed/24413561 http://dx.doi.org/10.1093/nar/gkt1361 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Nucleic Acid Enzymes
Hermann, Mario
Stillhard, Patrick
Wildner, Hendrik
Seruggia, Davide
Kapp, Viktor
Sánchez-Iranzo, Héctor
Mercader, Nadia
Montoliu, Lluís
Zeilhofer, Hanns Ulrich
Pelczar, Pawel
Binary recombinase systems for high-resolution conditional mutagenesis
title Binary recombinase systems for high-resolution conditional mutagenesis
title_full Binary recombinase systems for high-resolution conditional mutagenesis
title_fullStr Binary recombinase systems for high-resolution conditional mutagenesis
title_full_unstemmed Binary recombinase systems for high-resolution conditional mutagenesis
title_short Binary recombinase systems for high-resolution conditional mutagenesis
title_sort binary recombinase systems for high-resolution conditional mutagenesis
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973285/
https://www.ncbi.nlm.nih.gov/pubmed/24413561
http://dx.doi.org/10.1093/nar/gkt1361
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