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Binary recombinase systems for high-resolution conditional mutagenesis

机译:二元重组酶系统,用于高分辨率条件诱变

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摘要

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.
机译:使用从组织特异性启动子表达的CRE重组酶的条件诱变有助于基因功能和细胞谱系追踪分析。在这里,我们描述了两种新型双启动器驱动的条件诱变系统,设计用于更高的准确性和重组效率的更高。共同驱动器采用RE和DRE-受访者CRE的重组酶级联,仅当两种重组酶以预定的时间序列表达时,才能处理LOXP侧翼等位基因。这种独特的财产使共同司机是旨在解开细胞前体和成熟细胞类型之间的关系的顺序谱系追踪研究。 CO-CONTE设计用于高效的交叉条件转基因。它依赖于具有同时转录活性的高活性型转化性inteNIN和启动子,以将CRE重组酶从两个无活性前体片段重组。通过产生本地CRE,CO-CORCE达到超过本研究评估的所有其他二元SSR系统的重组率。共同司机和CO-CO11均显着扩展现有CRE响应等位基因的效用。

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  • 来源
    《Nucleic Acids Research》 |2014年第6期|共14页
  • 作者单位

    Institute of Laboratory Animal Science University of Zurich Sternwartstrasse 6 CH-8091 Zurich Switzerland;

    Institute of Laboratory Animal Science University of Zurich Sternwartstrasse 6 CH-8091 Zurich Switzerland;

    Institute of Pharmacology and Toxicology University of Zurich Winterthurerstrasse 190 CH-8057 Zurich Switzerland;

    National Centre for Biotechnology (CNB-CSIC) Darwin 3 28049 Madrid Spain;

    Institute of Laboratory Animal Science University of Zurich Sternwartstrasse 6 CH-8091 Zurich Switzerland;

    Program of Cardiovascular Development Department of Cardiovascular Development and Repair Centro Nacional de Investigaciones Cardiovasculares Carlos III calle Melchor Fernández Almagro 3 28029 Madrid Spain;

    Program of Cardiovascular Development Department of Cardiovascular Development and Repair Centro Nacional de Investigaciones Cardiovasculares Carlos III calle Melchor Fernández Almagro 3 28029 Madrid Spain;

    National Centre for Biotechnology (CNB-CSIC) Darwin 3 28049 Madrid Spain;

    Institute of Pharmacology and Toxicology University of Zurich Winterthurerstrasse 190 CH-8057 Zurich Switzerland;

    Institute of Laboratory Animal Science University of Zurich Sternwartstrasse 6 CH-8091 Zurich Switzerland;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
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