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CRISPR-Cas 介导的番茄基因敲除。

CRISPR-Cas-Mediated Gene Knockout in Tomato.

机构信息

Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.

VIB Center for Plant Systems Biology, Ghent, Belgium.

出版信息

Methods Mol Biol. 2020;2083:321-341. doi: 10.1007/978-1-4939-9952-1_25.

Abstract

Loss-of-function mutants are crucial for plant functional genomics studies. With the advent of CRISPR-Cas genome editing, generating null alleles for one or multiple specific gene(s) has become feasible for many plant species including tomato (Solanum lycopersicum). An easily programmable RNA-guided Cas endonuclease efficiently creates DNA double-strand breaks (DSBs) at targeted genomic sites that can be repaired by nonhomologous end joining (NHEJ) typically leading to small insertions or deletions that can produce null mutations. Here, we describe how to utilize CRISPR-Cas genome editing to obtain stable tomato gene knockout lines.

摘要

功能丧失突变体对于植物功能基因组学研究至关重要。随着 CRISPR-Cas 基因组编辑技术的出现,对于包括番茄(Solanum lycopersicum)在内的许多植物物种,生成一个或多个特定基因的无效等位基因已成为可能。一种易于编程的 RNA 指导 Cas 内切核酸酶可以在靶向基因组位点有效地产生 DNA 双链断裂(DSBs),这些断裂可以通过非同源末端连接(NHEJ)修复,通常导致小的插入或缺失,从而产生无效突变。在这里,我们将描述如何利用 CRISPR-Cas 基因组编辑来获得稳定的番茄基因敲除系。

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