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Vol 54(2020) N 1 p. 24-42; DOI 10.1134/S0026893320010069 Full Text

G.A. Gerashchenkov1*, N.A. Rozhnova1, B.R. Kuluev1, O.Yu. Kiryanova1,2, G.R. Gumerova1, A.V. Knyazev1, Z.R. Vershinina1, E.V. Mikhailova1, D.A. Chemeris1, R.T. Matniyazov1, An.Kh. Baimiev1, I.M. Gubaidullin3, Al.Kh. Baimiev1, A.V. Chemeris1

Design of Guide RNA for CRISPR/Cas Plant Genome Editing

1Institute of Biochemistry and Genetics, Russian Academy of Sciences, Ufa, 450054 Russia
2Ufa State Petroleum Technological University, Ufa, 450062 Russia
3Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, Ufa, 450075 Russia

*apomixis@anrb.ru
Received - 2019-05-31; Revised - 2019-05-31; Accepted - 2019-07-08

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.

CRISPR, Cas9, Cas12a, Cpf1, PAM, guide RNA, spacer, protospacer, target site, guide sequence, off-target, computer program, web-resource



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