Reilianum 孢子虫中 CRISPR/Cas9 核糖核蛋白介导的突变。

IF 1 Q3 BIOLOGY
Janina Werner, Weiliang Zuo, Gunther Doehlemann
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引用次数: 0

摘要

聚类规则间隔短回文重复序列/CRISPR相关蛋白9(CRISPR/Cas9)已成为丝状真菌诱变的最新技术。在这里,我们描述了一种由核糖核蛋白复合物(RNP)介导的CRISPR/Cas9诱变Sporisorium reilianum的方法。我们在体外用裂解试验测试了这种方法的效率,并在体内用表达 GFP 的雷氏孢子菌株进行了测试。我们利用这种方法,通过使用自动复制质粒进行选择,在 S. reilianum 中产生了无抗性标记的移帧突变体和基因敲除突变体。RNP 介导的 CRISPR/Cas9 提高了诱变效率,可用于所有类型的突变,并实现了 S. reilianum 的无标记基因组编辑。主要特点 - 首次在 S. reilianum 中应用 CRISPR/Cas9。- 在不整合抗性标记的情况下生成 S. reilianum 突变体。- 允许产生多基因敲除以及大基因组区域的删除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CRISPR/Cas9 Ribonucleoprotein-Mediated Mutagenesis in Sporisorium reilianum.

Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) has become the state of the art for mutagenesis in filamentous fungi. Here, we describe a ribonucleoprotein complex (RNP)-mediated CRISPR/Cas9 for mutagenesis in Sporisorium reilianum. The efficiency of the method was tested in vitro with a cleavage assay as well as in vivo with a GFP-expressing S. reilianum strain. We applied this method to generate frameshift- and knock-out mutants in S. reilianum without a resistance marker by using an auto-replicating plasmid for selection. The RNP-mediated CRISPR/Cas9 increased the mutagenesis efficiency, can be applied for all kinds of mutations, and enables a marker-free genome editing in S. reilianum. Key features • First CRISPR/Cas9 application in S. reilianum. • Generation of S. reilianum mutants without genomic integration of resistance marker. • Allows the generation of multiple gene knockouts as well as deletion of large genomic regions.

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