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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-3973285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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