Genome Editing Using Crispr/Cas System: New Era Genetic Technology in Agriculture to Boost Crop Output

P. Choudhary, M. Mushtaq, Anil Kumar Singh, Shazia Mukhtar, A. Shah, Gagan Mehta, P. Bakshi
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引用次数: 8

Abstract

Genome engineering with the RNA-guided CRISPR-Cas9 system in animals and plants is revolutionizing biology. First techniques of genome editing like zinc finger nucleases and synthetic nucleases called TALENs were a starting point but turned out to be expensive, difficult to handle and timeconsuming to engineer, limiting their widespread use, particularly for large scale, high-throughput studies. Moreover, these existing technologies depending on proteins as address labels and customizing new proteins for any new change to introduce in the DNA is a cumbersome process. Of the current generation of genome editing technologies, CRISPR-Cas9 is easier to use and more efficient and can be easily targeted to almost any genomic location of choice by a short RNA guide and has been successfully applied in many organisms, including model and crop plants. Together the system has the ability to detect specific sequences of letters within the genetic code and to cut DNA at a specific point. Simultaneously with other sequence-specific nucleases, CRISPR/ Cas9 has already breach the boundaries and made genetic engineering much more versatile, efficient and easy. There really doesn’t seem to be a limit in applications of CRISPR system extendable from bacteria to complex eukaryotic organisms including plants changing the pace and course of agricultural, Biomedicine and Biotechnological research in the future. This review provides an overview of recent advances in genome editing technologies in plants, and discusses how these can provide insights into current plant molecular biology research and molecular breeding technology.
利用Crispr/Cas系统进行基因组编辑:新时代农业基因技术提高作物产量
在动物和植物中使用rna引导的CRISPR-Cas9系统的基因组工程正在彻底改变生物学。最初的基因组编辑技术,如锌指核酸酶和被称为TALENs的合成核酸酶,是一个起点,但事实证明,这些技术昂贵、难以操作、耗时,限制了它们的广泛应用,尤其是在大规模、高通量的研究中。此外,这些现有的技术依赖于蛋白质作为地址标签,并为DNA中的任何新变化定制新的蛋白质是一个繁琐的过程。在当前一代基因组编辑技术中,CRISPR-Cas9更容易使用,效率更高,可以通过短RNA向导轻松靶向几乎任何选择的基因组位置,并已成功应用于许多生物,包括模型和作物植物。总之,该系统有能力检测遗传密码中的特定字母序列,并在特定点切割DNA。与其他序列特异性核酸酶同时,CRISPR/ Cas9已经突破了界限,使基因工程更加通用、高效和容易。CRISPR系统的应用似乎没有任何限制,它可以从细菌扩展到包括植物在内的复杂真核生物,改变未来农业、生物医学和生物技术研究的步伐和进程。本文综述了植物基因组编辑技术的最新进展,并讨论了这些技术如何为当前植物分子生物学研究和分子育种技术提供见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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