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      Efficient genetic transformation and CRISPR/Cas9‐mediated genome editing in Lemna aequinoctialis

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          Summary

          The fast growth, ease of metabolic labelling and potential for feedstock and biofuels production make duckweeds not only an attractive model system for understanding plant biology, but also a potential future crop. However, current duckweed research is constrained by the lack of efficient genetic manipulation tools. Here, we report a case study on genome editing in a duckweed species, Lemna aequinoctialis, using a fast and efficient transformation and CRISPR/Cas9 tool. By optimizing currently available transformation protocols, we reduced the duration time of Agrobacterium‐mediated transformation to 5–6 weeks with a success rate of over 94%. Based on the optimized transformation protocol, we generated 15 (14.3% success rate) biallelic La PDS mutants that showed albino phenotype using a CRISPR/Cas9 system. Investigations on CRISPR/Cas9‐mediated mutation spectrum among mutated L. aequinoctialis showed that most of mutations were short insertions and deletions. This study presents the first example of CRISPR/Cas9‐mediated genome editing in duckweeds, which will open new research avenues in using duckweeds for both basic and applied research.

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          Assaying chimeric genes in plants: The GUS gene fusion system

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            The CRISPR/Cas9 system produces specific and homozygous targeted gene editing in rice in one generation.

            The CRISPR/Cas9 system has been demonstrated to efficiently induce targeted gene editing in a variety of organisms including plants. Recent work showed that CRISPR/Cas9-induced gene mutations in Arabidopsis were mostly somatic mutations in the early generation, although some mutations could be stably inherited in later generations. However, it remains unclear whether this system will work similarly in crops such as rice. In this study, we tested in two rice subspecies 11 target genes for their amenability to CRISPR/Cas9-induced editing and determined the patterns, specificity and heritability of the gene modifications. Analysis of the genotypes and frequency of edited genes in the first generation of transformed plants (T0) showed that the CRISPR/Cas9 system was highly efficient in rice, with target genes edited in nearly half of the transformed embryogenic cells before their first cell division. Homozygotes of edited target genes were readily found in T0 plants. The gene mutations were passed to the next generation (T1) following classic Mendelian law, without any detectable new mutation or reversion. Even with extensive searches including whole genome resequencing, we could not find any evidence of large-scale off-targeting in rice for any of the many targets tested in this study. By specifically sequencing the putative off-target sites of a large number of T0 plants, low-frequency mutations were found in only one off-target site where the sequence had 1-bp difference from the intended target. Overall, the data in this study point to the CRISPR/Cas9 system being a powerful tool in crop genome engineering. © 2014 Society for Experimental Biology, Association of Applied Biologists and John Wiley & Sons Ltd.
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              Genome editing in rice and wheat using the CRISPR/Cas system.

              Targeted genome editing nucleases, such as zinc-finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs), are powerful tools for understanding gene function and for developing valuable new traits in plants. The clustered regularly interspersed short palindromic repeats (CRISPR)/Cas system has recently emerged as an alternative nuclease-based method for efficient and versatile genome engineering. In this system, only the 20-nt targeting sequence within the single-guide RNA (sgRNA) needs to be changed to target different genes. The simplicity of the cloning strategy and the few limitations on potential target sites make the CRISPR/Cas system very appealing. Here we describe a stepwise protocol for the selection of target sites, as well as the design, construction, verification and use of sgRNAs for sequence-specific CRISPR/Cas-mediated mutagenesis and gene targeting in rice and wheat. The CRISPR/Cas system provides a straightforward method for rapid gene targeting within 1-2 weeks in protoplasts, and mutated rice plants can be generated within 13-17 weeks.
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                Author and article information

                Contributors
                mayb@qibebt.ac.cn
                zhougk@qibebt.ac.cn
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                03 May 2019
                November 2019
                : 17
                : 11 ( doiID: 10.1111/pbi.v17.11 )
                : 2143-2152
                Affiliations
                [ 1 ] College of Resources and Environment Qingdao Agricultural University Qingdao China
                [ 2 ] Key Laboratory of Biofuels Qingdao Engineering Research Center of Biomass Resources and Environment Shandong Provincial Key Laboratory of Energy Genetics Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao China
                [ 3 ] Institute for Evolution and Biodiversity University of Münster Münster Germany
                Author notes
                [*] [* ] Correspondence (Tel +86‐532‐86080222; Fax +86‐532‐80662778; emails mayb@ 123456qibebt.ac.cn (YM), zhougk@ 123456qibebt.ac.cn (GZ))
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-2378-5122
                https://orcid.org/0000-0003-1458-5751
                Article
                PBI13128
                10.1111/pbi.13128
                6790374
                30972865
                98dc913b-b6a2-4aba-9ef7-18eb0eb3728d
                © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 February 2019
                : 03 April 2019
                : 08 April 2019
                Page count
                Figures: 4, Tables: 3, Pages: 10, Words: 8764
                Funding
                Funded by: National Key Technology Research and Development Program of China
                Award ID: 2015BAD15B01
                Funded by: Natural Science Foundation of China (NSFC) , open-funder-registry 10.13039/501100001809;
                Award ID: No.U1632140
                Award ID: No.31700308
                Award ID: No.31600285
                Funded by: Key projects of the Chinese Academy of Sciences , open-funder-registry 10.13039/501100002367;
                Award ID: ZDRW‐ZS‐2017‐2‐1
                Funded by: Science and technology service network plan of Chinese Academy of Science, Natural Science Foundation of Shandong Province
                Award ID: ZR2017BC089
                Funded by: Youth Innovation Promotion Association of CAS
                Award ID: 2018242
                Funded by: Qingdao National Science and technology project
                Award ID: 16‐6‐2‐40‐nsh
                Award ID: 17‐1‐1‐56‐jch
                Funded by: Taishan Scholar Program of Shandong
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                November 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.0 mode:remove_FC converted:14.10.2019

                Biotechnology
                agrobacterium‐mediated transformation,crispr/cas9,duckweed,genome editing
                Biotechnology
                agrobacterium‐mediated transformation, crispr/cas9, duckweed, genome editing

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