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CRISPR:从原核生物免疫系统到植物基因组编辑工具

CRISPR: From Prokaryotic Immune Systems to Plant Genome Editing Tools.

作者信息

Bandyopadhyay Anindya, Mazumdar Shamik, Yin Xiaojia, Quick William Paul

机构信息

C4 Rice Center, Genetics and Biotechnology Department, International Rice Research Institute, DAPO 7777, Manila, 1301, Philippines.

出版信息

Adv Exp Med Biol. 2017;1016:101-120. doi: 10.1007/978-3-319-63904-8_6.

Abstract

The clustered regularly interspaced short palindromic repeats (CRISPR) system is a prokaryotic adaptive immune system that has the ability to identify specific locations on the bacteriophage (phage) genome to create breaks in it, and internalize the phage genome fragments in its own genome as CRISPR arrays for memory-dependent resistance. Although CRISPR has been used in the dairy industry for a long time, it recently gained importance in the field of genome editing because of its ability to precisely target locations in a genome. This system has further been modified to locate and target any region of a genome of choice due to modifications in the components of the system. By changing the nucleotide sequence of the 20-nucleotide target sequence in the guide RNA, targeting any location is possible. It has found an application in the modification of plant genomes with its ability to generate mutations and insertions, thus helping to create new varieties of plants. With the ability to introduce specific sequences into the plant genome after cleavage by the CRISPR system and subsequent DNA repair through homology-directed repair (HDR), CRISPR ensures that genome editing can be successfully applied in plants, thus generating stronger and more improved traits. Also, the use of the CRISPR editing system can generate plants that are transgene-free and have mutations that are stably inherited, thus helping to circumvent current GMO regulations.

摘要

成簇规律间隔短回文重复序列(CRISPR)系统是一种原核生物适应性免疫系统,它能够识别噬菌体基因组上的特定位置并在其中产生断裂,然后将噬菌体基因组片段内化到自身基因组中形成CRISPR阵列,用于依赖记忆的抗性。尽管CRISPR在乳制品行业已经使用了很长时间,但由于其能够精确靶向基因组中的位置,最近在基因组编辑领域变得尤为重要。由于该系统组件的改进,它进一步被改造以定位和靶向任何选定基因组的区域。通过改变引导RNA中20个核苷酸靶序列的核苷酸序列,靶向任何位置都成为可能。它已在植物基因组修饰中得到应用,具有产生突变和插入的能力,从而有助于培育新的植物品种。通过CRISPR系统切割后能够将特定序列引入植物基因组,并通过同源定向修复(HDR)进行后续DNA修复,CRISPR确保基因组编辑能够成功应用于植物,从而产生更强和更优良的性状。此外,使用CRISPR编辑系统可以培育出无转基因且具有稳定遗传突变的植物,从而有助于规避当前的转基因生物法规。

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引用本文的文献

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