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CRISPR/Cas基因组编辑工具:在作物改良中的应用。

The CRISPR/Cas Genome-Editing Tool: Application in Improvement of Crops.

作者信息

Khatodia Surender, Bhatotia Kirti, Passricha Nishat, Khurana S M P, Tuteja Narendra

机构信息

Amity Institute of Biotechnology, Amity University Haryana Gurgaon, India.

Plant Molecular Biology Group, International Centre for Genetic Engineering and Biotechnology New Delhi, India.

出版信息

Front Plant Sci. 2016 Apr 19;7:506. doi: 10.3389/fpls.2016.00506. eCollection 2016.

Abstract

The Clustered Regularly Interspaced Short Palindromic Repeats associated Cas9/sgRNA system is a novel targeted genome-editing technique derived from bacterial immune system. It is an inexpensive, easy, most user friendly and rapidly adopted genome editing tool transforming to revolutionary paradigm. This technique enables precise genomic modifications in many different organisms and tissues. Cas9 protein is an RNA guided endonuclease utilized for creating targeted double-stranded breaks with only a short RNA sequence to confer recognition of the target in animals and plants. Development of genetically edited (GE) crops similar to those developed by conventional or mutation breeding using this potential technique makes it a promising and extremely versatile tool for providing sustainable productive agriculture for better feeding of rapidly growing population in a changing climate. The emerging areas of research for the genome editing in plants include interrogating gene function, rewiring the regulatory signaling networks and sgRNA library for high-throughput loss-of-function screening. In this review, we have described the broad applicability of the Cas9 nuclease mediated targeted plant genome editing for development of designer crops. The regulatory uncertainty and social acceptance of plant breeding by Cas9 genome editing have also been described. With this powerful and innovative technique the designer GE non-GM plants could further advance climate resilient and sustainable agriculture in the future and maximizing yield by combating abiotic and biotic stresses.

摘要

成簇规律间隔短回文重复序列相关的Cas9/sgRNA系统是一种源自细菌免疫系统的新型靶向基因组编辑技术。它是一种廉价、简便、用户友好且迅速被采用的基因组编辑工具,正在转变为革命性的范例。该技术能够在许多不同的生物体和组织中实现精确的基因组修饰。Cas9蛋白是一种RNA引导的内切核酸酶,用于在动植物中仅通过一段短RNA序列来识别靶标,从而产生靶向双链断裂。利用这一潜在技术培育与传统育种或诱变育种所培育的作物相似的基因编辑(GE)作物,使其成为一种有前景且用途极为广泛的工具,可为在气候变化背景下快速增长的人口提供可持续的高产农业。植物基因组编辑的新兴研究领域包括探究基因功能、重塑调控信号网络以及构建用于高通量功能丧失筛选的sgRNA文库。在本综述中,我们描述了Cas9核酸酶介导的靶向植物基因组编辑在培育定制作物方面的广泛适用性。我们还描述了Cas9基因组编辑在植物育种中的监管不确定性和社会接受度。借助这一强大且创新的技术,定制的基因编辑非转基因植物未来可进一步推动适应气候变化且可持续的农业发展,并通过抵御非生物和生物胁迫实现产量最大化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a14/4835450/2488bb16117c/fpls-07-00506-g001.jpg

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