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[用于CRISPR/Cas植物基因组编辑的引导RNA设计]

[Design of Guide RNA for CRISPR/Cas Plant Genome Editing].

作者信息

Gerashchenkov G A, Rozhnova N A, Kuluev B R, Kiryanova O Yu, Gumerova G R, Knyazev A V, Vershinina Z R, Mikhailova E V, Chemeris D A, Matniyazov R T, Baimiev An Kh, Gubaidullin I M, Baimiev Al Kh, Chemeris A V

机构信息

Institute of Biochemistry and Genetics, Russian Academy of Sciences, Ufa, 450054 Russia.

Ufa State Petroleum Technological University, Ufa, 450062 Russia.

出版信息

Mol Biol (Mosk). 2020 Jan-Feb;54(1):29-50. doi: 10.31857/S0026898420010061.

Abstract

CRISPR/Cas technology of genome editing is a powerful tool for making targeted changes in the DNA of various organisms, including plants. The choice of the precise nucleotide sequence (protospacer) in the gene to be edited is important in the design of guide RNA, which can be carried out by specialized software. We review and compare all the known on-line and off-line resources for guide RNA design, with special attention paid to tools capable of searching for off-target edits sites in plant genomes. The use of Cas12a may be preferable to Cas9. Techniques allowing C→T and G→A base editing without DNA cleavage are discussed along with the basic requirements for the design of effective and highly specific guide RNAs. Ways for improving guide RNA design software are presented. We also discuss the lesser risks of off-target editing in plant genomes as opposed to animal genomes. Examples of edited plant genomes including those that do not lead to the creation of transgenic plants are reviewed.

摘要

CRISPR/Cas基因组编辑技术是一种用于对包括植物在内的各种生物体的DNA进行靶向改变的强大工具。在设计引导RNA时,选择要编辑基因中的精确核苷酸序列(原间隔序列)很重要,这可以通过专门软件来完成。我们回顾并比较了所有已知的用于引导RNA设计的在线和离线资源,特别关注能够在植物基因组中搜索脱靶编辑位点的工具。使用Cas12a可能比Cas9更可取。讨论了无需DNA切割即可实现C→T和G→A碱基编辑的技术以及设计有效且高度特异性引导RNA的基本要求。提出了改进引导RNA设计软件的方法。我们还讨论了与动物基因组相比,植物基因组中脱靶编辑风险较小的情况。回顾了编辑植物基因组的实例,包括那些不会产生转基因植物的实例。

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