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      Allele exchange at the EPSPS locus confers glyphosate tolerance in cassava

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          Summary

          Effective weed control can protect yields of cassava ( Manihot esculenta) storage roots. Farmers could benefit from using herbicide with a tolerant cultivar. We applied traditional transgenesis and gene editing to generate robust glyphosate tolerance in cassava. By comparing promoters regulating expression of transformed 5‐enolpyruvylshikimate‐3‐phosphate synthase ( EPSPS) genes with various paired amino acid substitutions, we found that strong constitutive expression is required to achieve glyphosate tolerance during in vitro selection and in whole cassava plants. Using strategies that exploit homologous recombination ( HR) and nonhomologous end‐joining ( NHEJ) DNA repair pathways, we precisely introduced the best‐performing allele into the cassava genome, simultaneously creating a promoter swap and dual amino acid substitutions at the endogenous EPSPS locus. Primary EPSPS‐edited plants were phenotypically normal, tolerant to high doses of glyphosate, with some free of detectable T‐ DNA integrations. Our methods demonstrate an editing strategy for creating glyphosate tolerance in crop plants and demonstrate the potential of gene editing for further improvement of cassava.

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          Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9.

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            Golden Gate Shuffling: A One-Pot DNA Shuffling Method Based on Type IIs Restriction Enzymes

            We have developed a protocol to assemble in one step and one tube at least nine separate DNA fragments together into an acceptor vector, with 90% of recombinant clones obtained containing the desired construct. This protocol is based on the use of type IIs restriction enzymes and is performed by simply subjecting a mix of 10 undigested input plasmids (nine insert plasmids and the acceptor vector) to a restriction-ligation and transforming the resulting mix in competent cells. The efficiency of this protocol allows generating libraries of recombinant genes by combining in one reaction several fragment sets prepared from different parental templates. As an example, we have applied this strategy for shuffling of trypsinogen from three parental templates (bovine cationic trypsinogen, bovine anionic trypsinogen and human cationic trypsinogen) each divided in 9 separate modules. We show that one round of shuffling using the 27 trypsinogen entry plasmids can easily produce the 19,683 different possible combinations in one single restriction-ligation and that expression screening of a subset of the library allows identification of variants that can lead to higher expression levels of trypsin activity. This protocol, that we call ‘Golden Gate shuffling’, is robust, simple and efficient, can be performed with templates that have no homology, and can be combined with other shuffling protocols in order to introduce any variation in any part of a given gene.
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              Efficient and transgene-free genome editing in wheat through transient expression of CRISPR/Cas9 DNA or RNA

              Editing plant genomes is technically challenging in hard-to-transform plants and usually involves transgenic intermediates, which causes regulatory concerns. Here we report two simple and efficient genome-editing methods in which plants are regenerated from callus cells transiently expressing CRISPR/Cas9 introduced as DNA or RNA. This transient expression-based genome-editing system is highly efficient and specific for producing transgene-free and homozygous wheat mutants in the T0 generation. We demonstrate our protocol to edit genes in hexaploid bread wheat and tetraploid durum wheat, and show that we are able to generate mutants with no detectable transgenes. Our methods may be applicable to other plant species, thus offering the potential to accelerate basic and applied plant genome-engineering research.
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                Author and article information

                Contributors
                ntaylor@danforthcenter.org
                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
                22 January 2018
                July 2018
                : 16
                : 7 ( doiID: 10.1111/pbi.2018.16.issue-7 )
                : 1275-1282
                Affiliations
                [ 1 ] Department of Genetics, Cell Biology, & Development and Center for Genome Engineering University of Minnesota Minneapolis MN USA
                [ 2 ] Donald Danforth Plant Science Center St. Louis MO USA
                [ 3 ]Present address: KWS Gateway Research Center St. Louis MO USA
                [ 4 ]Present address: Inari Agriculture Inc 200 Sidney St Suite 340, Cambridge MA 02139 USA
                [ 5 ]Present address: Elemental Enzymes St. Louis MO USA
                [ 6 ]Present address: Monsanto St. Louis MO USA
                Author notes
                [*] [* ] Correspondence (Tel 314 587 1257; fax 314 587 1357; email ntaylor@ 123456danforthcenter.org )
                [†]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-5426-2247
                Article
                PBI12868
                10.1111/pbi.12868
                5999311
                29223136
                315f34d6-64e8-439d-9970-6ac85aa0e918
                © 2017 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
                : 19 July 2017
                : 22 November 2017
                : 03 December 2017
                Page count
                Figures: 3, Tables: 1, Pages: 8, Words: 5475
                Funding
                Funded by: Bill & Melinda Gates Foundation
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                pbi12868
                July 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.3 mode:remove_FC converted:05.07.2018

                Biotechnology
                gene replacement,gene editing,cassava,herbicide tolerance
                Biotechnology
                gene replacement, gene editing, cassava, herbicide tolerance

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