Impact of predictive selection of LbCas12a CRISPR RNAs upon on- and off-target editing rates in soybean

被引:1
作者
Rymarquis, Linda [1 ]
Wu, Chenxi [1 ]
Hohorst, Diane [1 ]
Vega-Sanchez, Miguel [1 ]
Mullen, Thomas E. [2 ]
Vemulapalli, Vijetha [2 ]
Smith, Douglas R. [2 ]
机构
[1] Bayer Crop Sci, Chesterfield, MO 63017 USA
[2] SeQure DX, Waltham, MA USA
关键词
genome editing; gRNA design; LbCas12a; GENOME; DESIGN; CPF1; SPECIFICITIES; ENDONUCLEASE;
D O I
10.1002/pld3.627
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Clustered regularly interspaced short palindromic repeats (CRISPR) technology has revolutionized creating targeted genetic variation in crops. Although CRISPR enzymes have been reported to have high sequence-specificity, careful design of the editing reagents can also reduce unintended edits at highly homologous sites. This work details the first large-scale study of the heritability of on-target edits and the rate of edits at off-target sites in soybean (Glycine max), assaying similar to 700 T1 plants each resulting from transformation with LbCas12a constructs containing CRISPR RNAs (crRNAs) predicted to be either "unique" with no off-target sites or "promiscuous" with >10 potential off-targets in the soybean genome. Around 80% of the on-target edits observed in T0 plants were inherited in the T1 generation, and similar to 49% of the total observed on-target edits in T1 were not observed at T0, indicating continued activity of LbCas12a throughout the life cycle of the plant. In planta editing at off-target sites was observed for the Promiscuous but not the Unique crRNA. Examination of the edited off-target sites revealed that LbCas12a was highly tolerant to mismatches between the crRNA and target site in bases 21-23 relative to the start of the protospacer, but even a single mismatch in the first 20 nt drastically reduced the editing rate. In addition, edits at off-target sites have lower inheritance rates than on-target edits, suggesting that they occur later in the plant's lifecycle. Plants with a desired on-target edit and no off-target edits could be identified in the T1 generation for 100% of the T0 plants edited with the Unique crRNA compared with the 65% of T0 plants edited with the Promiscuous crRNA. This confirms that proper crRNA selection can reduce or eliminate off-target editing. Even when potential off-target sites are predicted, plants containing only the intended edits can still be identified and propagated.
引用
收藏
页数:10
相关论文
共 47 条
  • [21] Genome-wide specificities of CRISPR-Cas Cpf1 nucleases in human cells
    Kleinstiver, Benjamin P.
    Tsai, Shengdar Q.
    Prew, Michelle S.
    Nguyen, Nhu T.
    Welch, Moira M.
    Lopez, Jose M.
    McCaw, Zachary R.
    Aryee, Martin J.
    Joung, J. Keith
    [J]. NATURE BIOTECHNOLOGY, 2016, 34 (08) : 869 - +
  • [22] Demonstration of targeted crossovers in hybrid maize using CRISPR technology
    Kouranov, Andrei
    Armstrong, Charles
    Shrawat, Ashok
    Sidorov, Vladimir
    Huesgen, Scott
    Lemke, Bryce
    Boyle, Timothy
    Gasper, Michelle
    Lawrence, Richard
    Yang, Samuel
    [J]. COMMUNICATIONS BIOLOGY, 2022, 5 (01)
  • [23] A systematic evaluation of nucleotide properties for CRISPR sgRNA design
    Kuan, Pei Fen
    Powers, Scott
    He, Shuyao
    Li, Kaiqiao
    Zhao, Xiaoyu
    Huang, Bo
    [J]. BMC BIOINFORMATICS, 2017, 18
  • [24] Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
    Langmead, Ben
    Trapnell, Cole
    Pop, Mihai
    Salzberg, Steven L.
    [J]. GENOME BIOLOGY, 2009, 10 (03):
  • [25] Whole genome sequencing reveals rare off-target mutations and considerable inherent genetic or/and somaclonal variations in CRISPR/Cas9-edited cotton plants
    Li, Jianying
    Manghwar, Hakim
    Sun, Lin
    Wang, Pengcheng
    Wang, Guanying
    Sheng, Hanyan
    Zhang, Jie
    Liu, Hao
    Qin, Lei
    Rui, Hangping
    Li, Bo
    Lindsey, Keith
    Daniell, Henry
    Jin, Shuangxia
    Zhang, Xianlong
    [J]. PLANT BIOTECHNOLOGY JOURNAL, 2019, 17 (05) : 858 - 868
  • [26] BREEDIT: a multiplex genome editing strategy to improve complex quantitative traits in maize
    Lorenzo, Christian Damian
    Debray, Kevin
    Herwegh, Denia
    Develtere, Ward
    Impens, Lennert
    Schaumont, Dries
    Vandeputte, Wout
    Aesaert, Stijn
    Coussens, Griet
    De Boe, Yara
    Demuynck, Kirin
    Van Hautegem, Tom
    Pauwels, Laurens
    Jacobs, Thomas B.
    Ruttink, Tom
    Nelissen, Hilde
    Inze, Dirk
    [J]. PLANT CELL, 2023, 35 (01) : 218 - 238
  • [27] New Strategies to Overcome Present CRISPR/Cas9 Limitations in Apple and Pear: Efficient Dechimerization and Base Editing
    Malabarba, Jaiana
    Chevreau, Elisabeth
    Dousset, Nicolas
    Veillet, Florian
    Moizan, Julie
    Vergne, Emilie
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (01) : 1 - 20
  • [28] Defining genome-wide CRISPR-Cas genome-editing nuclease activity with GUIDE-seq
    Malinin, Nikolay L.
    Lee, GaHyun
    Lazzarotto, Cicera R.
    Li, Yichao
    Zheng, Zongli
    Nguyen, Nhu T.
    Liebers, Matthew
    Topkar, Ved V.
    Iafrate, A. John
    Le, Long P.
    Aryee, Martin J.
    Joung, J. Keith
    Tsai, Shengdar Q.
    [J]. NATURE PROTOCOLS, 2021, 16 (12) : 5593 - +
  • [29] CRISPR/Cas Systems in Genome Editing: Methodologies and Tools for sgRNA Design, Off-Target Evaluation, and Strategies to Mitigate Off-Target Effects
    Manghwar, Hakim
    Li, Bo
    Ding, Xiao
    Hussain, Amjad
    Lindsey, Keith
    Zhang, Xianlong
    Jin, Shuangxia
    [J]. ADVANCED SCIENCE, 2020, 7 (06)
  • [30] Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing
    Mengstie, Misganaw Asmamaw
    Wondimu, Belay Zawdie
    [J]. BIOLOGICS-TARGETS & THERAPY, 2021, 15 : 353 - 361