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用于植物基因组编辑的多重CRISPR-Cas9系统的快速构建

Rapid Construction of Multiplexed CRISPR-Cas9 Systems for Plant Genome Editing.

作者信息

Lowder Levi, Malzahn Aimee, Qi Yiping

机构信息

Department of Biology, University of Maryland, College Park, N 108 Howell Science Complex, Greenville, NC, 27858, USA.

Department of Plant Science and Landscape Architecture, University of Maryland, College Park, MD, 20742, USA.

出版信息

Methods Mol Biol. 2017;1578:291-307. doi: 10.1007/978-1-4939-6859-6_25.

Abstract

Multiplex CRISPR-Cas9 nuclease mediated genome editing is an efficient method for disrupting gene function in plants. Use of CRISPR-Cas9 has escalated rapidly in recent years and is expected to become routine practice in molecular biology and related fields of research. Due to the relatively novel and widespread adoption of this technology, first-time users may not have regular access to experienced guidance or technical support from peers or mentors. Here, we offer guidance and technical support in the form of a detailed and tested protocol for simultaneous targeting of three separate loci on the TRANSPARENT TESTA 4 (TT4) gene in Arabidopsis thaliana using multiplex CRISPR-Cas9. Although we target multiple loci on a single gene in Arabidopsis, the same approach can be used to target multiple genes or alleles in other plant species as well. We recommend the use of a molecular toolkit to streamline the process and make recommendations for this type of approach. The protocol starts with an overview of the reagents and covers designing of gRNAs and assembly of components into a final T-DNA delivery molecule through Golden Gate cloning and Multisite Gateway LR recombination.

摘要

多重CRISPR-Cas9核酸酶介导的基因组编辑是一种破坏植物基因功能的有效方法。近年来,CRISPR-Cas9的使用迅速增加,预计将成为分子生物学及相关研究领域的常规操作。由于这项技术相对新颖且应用广泛,首次使用者可能无法经常获得同行或导师的经验指导或技术支持。在此,我们提供指导和技术支持,形式为一份详细且经过测试的方案,用于使用多重CRISPR-Cas9同时靶向拟南芥中透明种皮4(TT4)基因上的三个独立位点。虽然我们在拟南芥的单个基因上靶向多个位点,但相同的方法也可用于靶向其他植物物种中的多个基因或等位基因。我们建议使用分子工具包来简化流程,并针对此类方法提出建议。该方案首先概述了试剂,涵盖gRNA的设计以及通过金门克隆和多位点Gateway LR重组将组件组装成最终的T-DNA递送分子。

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