基因编辑工具的进展、影响和在植物中的成功:综述

IF 4.9 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in genome editing Pub Date : 2023-12-07 DOI:10.3389/fgeed.2023.1272678
Suman Jyoti Bhuyan, Manoj Kumar, Pandurang Ramrao Devde, A. C. Rai, Amit Kumar Mishra, Prashant Kumar Singh, K. Siddique
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引用次数: 0

摘要

在作物改良计划中,通过各种诱变技术进行基因修饰。在这些诱变工具中,传统方法包括化学诱变和辐射诱变,会导致基因组发生脱靶和意外突变。然而,与诱导诱变和育种群体中自然发生的突变相比,最近的进展是引入了用于基因编辑的定点定向核酸酶(SDNs),从而大大减少了基因组中的脱靶变化。近几十年来,SDNs 使基因工程发生了革命性变化,实现了精确的基因编辑。同源定向修复(HDR)是一种广泛使用的方法,在某些植物物种中可有效实现精确的碱基替换和基因改变。然而,由于 HDR 在植物细胞中的效率低下,以及非同源末端连接(NHEJ)这一易出错的修复途径的普遍存在,该方法的应用受到了限制。CRISPR-Cas 的发现改变了这一领域的游戏规则。该系统通过在基因组中产生双链断裂(DSB)来诱导突变,并通过相关的修复途径(如 NHEJ)对其进行修复。因此,CRISPR-Cas 系统已被广泛用于转化植物,以进行基因功能分析和增强理想性状。近年来,研究人员在基因工程领域取得了重大进展,尤其是在理解 CRISPR-Cas 机制方面。由此产生了各种 CRISPR-Cas 变体,包括 CRISPR-Cas13、CRISPR 干扰、CRISPR 激活、碱基编辑器、primes 编辑器,以及用于基因工程的可裂解蛋白质的新型 CRISPR-Cas 系统 CRASPASE。此外,基因编辑技术(如素编辑器和碱基编辑器方法)为植物基因组工程提供了绝佳的机会。这些尖端工具为快速操作植物基因组开辟了新途径。这篇综述文章全面概述了植物基因工程的现状,重点介绍了最近开发的基因改变工具及其在植物研究中的潜在应用。
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Progress in gene editing tools, implications and success in plants: a review
Genetic modifications are made through diverse mutagenesis techniques for crop improvement programs. Among these mutagenesis tools, the traditional methods involve chemical and radiation-induced mutagenesis, resulting in off-target and unintended mutations in the genome. However, recent advances have introduced site-directed nucleases (SDNs) for gene editing, significantly reducing off-target changes in the genome compared to induced mutagenesis and naturally occurring mutations in breeding populations. SDNs have revolutionized genetic engineering, enabling precise gene editing in recent decades. One widely used method, homology-directed repair (HDR), has been effective for accurate base substitution and gene alterations in some plant species. However, its application has been limited due to the inefficiency of HDR in plant cells and the prevalence of the error-prone repair pathway known as non-homologous end joining (NHEJ). The discovery of CRISPR-Cas has been a game-changer in this field. This system induces mutations by creating double-strand breaks (DSBs) in the genome and repairing them through associated repair pathways like NHEJ. As a result, the CRISPR-Cas system has been extensively used to transform plants for gene function analysis and to enhance desirable traits. Researchers have made significant progress in genetic engineering in recent years, particularly in understanding the CRISPR-Cas mechanism. This has led to various CRISPR-Cas variants, including CRISPR-Cas13, CRISPR interference, CRISPR activation, base editors, primes editors, and CRASPASE, a new CRISPR-Cas system for genetic engineering that cleaves proteins. Moreover, gene editing technologies like the prime editor and base editor approaches offer excellent opportunities for plant genome engineering. These cutting-edge tools have opened up new avenues for rapidly manipulating plant genomes. This review article provides a comprehensive overview of the current state of plant genetic engineering, focusing on recently developed tools for gene alteration and their potential applications in plant research.
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CiteScore
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