Precise gene replacement in plants through CRISPR/Cas genome editing technology: current status and future perspectives

IF 4.6 4区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY aBIOTECH Pub Date : 2019-11-07 DOI:10.1007/s42994-019-00009-7
Shaoya Li, Lanqin Xia
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引用次数: 25

Abstract

CRISPR/Cas, as a simple, versatile, robust and cost-effective system for genome manipulation, has dominated the genome editing field over the past few years. The application of CRISPR/Cas in crop improvement is particularly important in the context of global climate change, as well as diverse agricultural, environmental and ecological challenges. Various CRISPR/Cas toolboxes have been developed and allow for targeted mutagenesis at specific genome loci, transcriptome regulation and epigenome editing, base editing, and precise targeted gene/allele replacement or tagging in plants. In particular, precise replacement of an existing allele with an elite allele in a commercial variety through homology-directed repair (HDR) is a holy grail in genome editing for crop improvement as it has been very difficult, laborious and time-consuming to introgress the elite alleles into commercial varieties without any linkage drag from parental lines within a few generations in crop breeding practice. However, it still remains very challenging in crop plants. This review intends to provide an informative summary of the latest development and breakthroughs in gene replacement using CRISPR/Cas technology, with a focus on achievements, potential mechanisms and future perspectives in plant biological science as well as crop improvement.

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CRISPR/Cas基因组编辑技术在植物中的精确基因替换:现状和未来展望
CRISPR/Cas作为一种简单、通用、稳健且具有成本效益的基因组操作系统,在过去几年中一直主导着基因组编辑领域。在全球气候变化以及各种农业、环境和生态挑战的背景下,CRISPR/Cas在作物改良中的应用尤为重要。已经开发了各种CRISPR/Cas工具箱,可以在特定的基因组位点进行靶向诱变、转录组调控和表观基因组编辑、碱基编辑,以及在植物中进行精确的靶向基因/等位基因替换或标记。特别是,通过同源定向修复(HDR)用商业品种中的精英等位基因精确替换现有等位基因是作物改良基因组编辑中的圣杯,因为这非常困难,在作物育种实践中,在几代内将优良等位基因导入到商业品种中而不受亲本系的任何连锁阻力是费时费力的。然而,它在作物中仍然非常具有挑战性。本综述旨在对利用CRISPR/Cas技术进行基因替换的最新进展和突破进行信息总结,重点介绍植物生物科学和作物改良方面的成就、潜在机制和未来前景。
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来源期刊
CiteScore
7.70
自引率
2.80%
发文量
0
期刊最新文献
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