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CRISPR/Cas系统在培育抗病原体植物中的应用。

Application of the CRISPR/Cas System for Generation of Pathogen-Resistant Plants.

作者信息

Makarova S S, Khromov A V, Spechenkova N A, Taliansky M E, Kalinina N O

机构信息

Doka-Gene Technology Ltd., 141880 Rogachevo, Moscow Region, Russia.

Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119991, Russia.

出版信息

Biochemistry (Mosc). 2018 Dec;83(12):1552-1562. doi: 10.1134/S0006297918120131.

Abstract

The use of the CRISPR/Cas9 prokaryotic adaptive immune system has led to a breakthrough in targeted genome editing in eukaryotes. The CRISPR/Cas technology allows to generate organisms with desirable characteristics by introducing deletions/insertions into selected genome loci resulting in the knockout or modification of target genes. This review focuses on the current state of the CRISPR/Cas use for the generation of plants resistant to viruses, bacteria, and parasitic fungi. Resistance to DNA- and RNA-containing viruses is usually provided by expression in transgenic plants of the Cas endonuclease gene and short guide RNAs (sgRNAs) targeting certain sites in the viral or the host plant genomes to ensure either direct cleavage of the viral genome or modification of the plant host genome in order to decrease the efficiency of virus replication. Editing of plant genes involved in the defense response to pathogens increases plants resistance to bacteria and pathogenic fungi. The review explores strategies and prospects of the development of pathogen-resistant plants with a focus on the generation of non-transgenic (non-genetically modified) organisms, in particular, by using plasmid (DNA)-free systems for delivery of the Cas/sgRNA editing complex into plant cells.

摘要

CRISPR/Cas9原核生物适应性免疫系统的应用在真核生物靶向基因组编辑方面取得了突破。CRISPR/Cas技术通过在选定的基因组位点引入缺失/插入,从而实现靶基因的敲除或修饰,进而培育出具有理想特性的生物体。本综述聚焦于CRISPR/Cas技术在培育抗病毒、细菌和寄生真菌植物方面的应用现状。对含DNA和RNA病毒的抗性通常通过在转基因植物中表达Cas核酸内切酶基因和靶向病毒或宿主植物基因组特定位点的短引导RNA(sgRNA)来实现,以确保直接切割病毒基因组或修饰植物宿主基因组,从而降低病毒复制效率。对参与病原体防御反应的植物基因进行编辑可增强植物对细菌和致病真菌的抗性。本综述探讨了培育抗病植物的策略和前景,重点关注非转基因生物体的培育,特别是通过使用无质粒(DNA)系统将Cas/sgRNA编辑复合体导入植物细胞。

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