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      Defined tetra-allelic gene disruption of the 4-coumarate:coenzyme A ligase 1 (Pv4CL1) gene by CRISPR/Cas9 in switchgrass results in lignin reduction and improved sugar release

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          Abstract

          Background

          The development of genome editing technologies offers new prospects in improving bioenergy crops like switchgrass ( Panicum virgatum). Switchgrass is an outcrossing species with an allotetraploid genome (2 n = 4 x = 36), a complexity which forms an impediment to generating homozygous knock-out plants. Lignin, a major component of the plant cell wall and a contributor to cellulosic feedstock’s recalcitrance to decomposition, stands as a barrier to efficient biofuel production by limiting enzyme access to cell wall polymers during the fermentation process.

          Results

          We developed a CRISPR/Cas9 genome editing system in switchgrass to target a key enzyme involved in the early steps of monolignol biosynthesis, 4-Coumarate:coenzyme A ligase (4CL). Three 4CL genes, Pv4CL1, Pv4CL2, and Pv4CL3, were identified in switchgrass. Expression analysis revealed that Pv4CL1 transcripts were more abundant in the stem than in the leaf, while Pv4CL2 transcripts were barely detectable and Pv4CL3 was mainly expressed in the leaf. Pv4CL1 was selected as the target for CRISPR/Cas9 editing because of its preferential expression in highly lignified stem tissues. Specific guide RNA was constructed to target Pv4CL1. After introducing the construct into switchgrass calli, 39 transgenic plants were regenerated. Using two rounds of PCR screening and sequencing, four plants were confirmed to have tetra-allelic mutations simultaneously. The Pv4CL1 knock-out plants had reduced cell wall thickness, an 8–30% reduction in total lignin content, a 7–11% increase in glucose release, and a 23–32% increase in xylose release.

          Conclusion

          This study established a successful CRISPR/Cas9 system in switchgrass with mutation efficiency reaching 10%. The system allows the precise targeting of the selected Pv4CL1 gene to create switchgrass knock-out mutant plants with decreased lignin content and reduced recalcitrance.

          Electronic supplementary material

          The online version of this article (10.1186/s13068-017-0972-0) contains supplementary material, which is available to authorized users.

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          Most cited references25

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          Plant genome editing made easy: targeted mutagenesis in model and crop plants using the CRISPR/Cas system

          Targeted genome engineering (also known as genome editing) has emerged as an alternative to classical plant breeding and transgenic (GMO) methods to improve crop plants. Until recently, available tools for introducing site-specific double strand DNA breaks were restricted to zinc finger nucleases (ZFNs) and TAL effector nucleases (TALENs). However, these technologies have not been widely adopted by the plant research community due to complicated design and laborious assembly of specific DNA binding proteins for each target gene. Recently, an easier method has emerged based on the bacterial type II CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated) immune system. The CRISPR/Cas system allows targeted cleavage of genomic DNA guided by a customizable small noncoding RNA, resulting in gene modifications by both non-homologous end joining (NHEJ) and homology-directed repair (HDR) mechanisms. In this review we summarize and discuss recent applications of the CRISPR/Cas technology in plants.
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            Gene-edited CRISPR mushroom escapes US regulation.

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              Silencing of 4-coumarate:coenzyme A ligase in switchgrass leads to reduced lignin content and improved fermentable sugar yields for biofuel production.

              • The lignin content of feedstock has been proposed as one key agronomic trait impacting biofuel production from lignocellulosic biomass. 4-Coumarate:coenzyme A ligase (4CL) is one of the key enzymes involved in the monolignol biosynthethic pathway. • Two homologous 4CL genes, Pv4CL1 and Pv4CL2, were identified in switchgrass (Panicum virgatum) through phylogenetic analysis. Gene expression patterns and enzymatic activity assays suggested that Pv4CL1 is involved in monolignol biosynthesis. Stable transgenic plants were obtained with Pv4CL1 down-regulated. • RNA interference of Pv4CL1 reduced extractable 4CL activity by 80%, leading to a reduction in lignin content with decreased guaiacyl unit composition. Altered lignification patterns in the stems of RNAi transgenic plants were observed with phloroglucinol-HCl staining. The transgenic plants also had uncompromised biomass yields. After dilute acid pretreatment, the low lignin transgenic biomass had significantly increased cellulose hydrolysis (saccharification) efficiency. • The results demonstrate that Pv4CL1, but not Pv4CL2, is the key 4CL isozyme involved in lignin biosynthesis, and reducing lignin content in switchgrass biomass by silencing Pv4CL1 can remarkably increase the efficiency of fermentable sugar release for biofuel production. © 2011 The Authors. New Phytologist © 2011 New Phytologist Trust.
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                Author and article information

                Contributors
                archegon48@gmail.com
                yoocg80@gmail.com
                amflanagan@noble.org
                puy1@ornl.gov
                sdebnath@noble.org
                yge@noble.org
                aragausk@utk.edu
                zywang@noble.org
                Journal
                Biotechnol Biofuels
                Biotechnol Biofuels
                Biotechnology for Biofuels
                BioMed Central (London )
                1754-6834
                30 November 2017
                30 November 2017
                2017
                : 10
                : 284
                Affiliations
                [1 ]ISNI 0000 0004 0370 5663, GRID grid.419447.b, Noble Research Institute, ; Ardmore, OK 73401 USA
                [2 ]ISNI 0000 0004 0446 2659, GRID grid.135519.a, BioEnergy Science Center, , Oak Ridge National Laboratory, ; Oak Ridge, TN 37831 USA
                [3 ]ISNI 0000 0004 0446 2659, GRID grid.135519.a, Joint Institute for Biological Sciences, Biosciences Division, , Oak Ridge National Laboratory, ; Oak Ridge, TN 37830 USA
                [4 ]ISNI 0000 0001 2315 1184, GRID grid.411461.7, Department of Chemical and Biomolecular Engineering, , University of Tennessee, ; Knoxville, TN 37996 USA
                [5 ]ISNI 0000 0001 2315 1184, GRID grid.411461.7, Center for Renewable Carbon, Department of Forestry, Wildlife, and Fisheries, , University of Tennessee Institute of Agriculture, ; Knoxville, TN 37996 USA
                Author information
                http://orcid.org/0000-0002-6835-7917
                Article
                972
                10.1186/s13068-017-0972-0
                5708096
                29213323
                063e3d32-1805-4bcb-bc50-0e2c2687e9b2
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 16 June 2017
                : 18 November 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100006132, Office of Science;
                Award ID: DE-AC05-00OR22725
                Award Recipient :
                Funded by: The Samuel Roberts Noble Foundation
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Biotechnology
                genome editing,crispr/cas9,switchgrass,panicum virgatum,bioenergy,lignin biosynthesis,4-coumarate:coenzyme a ligase,4cl,sugar release

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