Tailoring poplar lignin without yield penalty by combining a null and haploinsufficient CINNAMOYL-CoA REDUCTASE2 allele.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
06 10 2020
Historique:
received: 31 03 2020
accepted: 16 09 2020
entrez: 7 10 2020
pubmed: 8 10 2020
medline: 30 10 2020
Statut: epublish

Résumé

Lignin causes lignocellulosic biomass recalcitrance to enzymatic hydrolysis. Engineered low-lignin plants have reduced recalcitrance but often exhibit yield penalties, offsetting their gains in fermentable sugar yield. Here, CRISPR/Cas9-generated CCR2(-/*) line 12 poplars have one knockout CCR2 allele while the other contains a 3-bp deletion, resulting in a 114I115A-to-114T conversion in the corresponding protein. Despite having 10% less lignin, CCR2(-/*) line 12 grows normally. On a plant basis, the saccharification efficiency of CCR2(-/*) line 12 is increased by 25-41%, depending on the pretreatment. Analysis of monoallelic CCR2 knockout lines shows that the reduced lignin amount in CCR2(-/*) line 12 is due to the combination of a null and the specific haploinsufficient CCR2 allele. Analysis of another CCR2(-/*) line shows that depending on the specific CCR2 amino-acid change, lignin amount and growth can be affected to different extents. Our findings open up new possibilities for stably fine-tuning residual gene function in planta.

Identifiants

pubmed: 33024118
doi: 10.1038/s41467-020-18822-w
pii: 10.1038/s41467-020-18822-w
pmc: PMC7538556
doi:

Substances chimiques

Plant Proteins 0
Lignin 9005-53-2
Aldehyde Oxidoreductases EC 1.2.-
cinnamoyl CoA reductase EC 1.2.1.44

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

5020

Références

Vanholme, R., De Meester, B., Ralph, J. & Boerjan, W. Lignin biosynthesis and its integration into metabolism. Curr. Opin. Biotechnol. 56, 230–239 (2019).
doi: 10.1016/j.copbio.2019.02.018
Mansfield, S. D., Kang, K.-Y. & Chapple, C. Designed for deconstruction—poplar trees altered in cell wall lignification improve the efficacy of bioethanol production. N. Phytol. 194, 91–101 (2012).
doi: 10.1111/j.1469-8137.2011.04031.x
Van Acker, R. et al. Improved saccharification and ethanol yield from field-grown transgenic poplar deficient in cinnamoyl-CoA reductase. Proc. Natl Acad. Sci. USA 111, 845–850 (2014).
doi: 10.1073/pnas.1321673111
Voelker, S. L. et al. Antisense down-regulation of 4CL expression alters lignification, tree growth, and saccharification potential of field-grown poplar. Plant Physiol. 154, 874–886 (2010).
doi: 10.1104/pp.110.159269
Leplé, J.-C. et al. Downregulation of cinnamoyl-coenzyme A reductase in poplar: multiple-level phenotyping reveals effects on cell wall polymer metabolism and structure. Plant Cell 19, 3669–3691 (2007).
doi: 10.1105/tpc.107.054148
Vanholme, R. et al. Caffeoyl shikimate esterase (CSE) is an enzyme in the lignin biosynthetic pathway in Arabidopsis. Science 341, 1103–1106 (2013).
doi: 10.1126/science.1241602
De Meester, B. et al. Vessel-specific reintroduction of CINNAMOYL-COA REDUCTASE1 (CCR1) in dwarfed ccr1 mutants restores vessel and xylary fiber integrity and increases biomass. Plant Physiol. 176, 611–633 (2018).
doi: 10.1104/pp.17.01462
Muro-Villanueva, F., Mao, X. & Chapple, C. Linking phenylpropanoid metabolism, lignin deposition, and plant growth inhibition. Curr. Opin. Biotechnol. 56, 202–208 (2019).
doi: 10.1016/j.copbio.2018.12.008
Pan, H. et al. Structural studies of cinnamoyl-CoA reductase and cinnamyl-alcohol dehydrogenase, key enzymes of monolignol biosynthesis. Plant Cell 26, 3709–3727 (2014).
doi: 10.1105/tpc.114.127399
Sonawane, P., Vishwakarma, R. K. & Khan, B. M. Biochemical characterization of recombinant cinnamoyl CoA reductase 1 (Ll-CCRH1) from Leucaena leucocephala. Int. J. Biol. Macromol. 58, 154–159 (2013).
doi: 10.1016/j.ijbiomac.2013.03.050
Chao, N. et al. Characterization of the cinnamoyl-CoA reductase (CCR) gene family in Populus tomentosa reveals the enzymatic active sites and evolution of CCR. Planta 245, 61–75 (2017).
doi: 10.1007/s00425-016-2591-6
Tsai, C.-J. & Xue, L.-J. CRISPRing into the woods. GM Crops Food 6, 206–215 (2015).
doi: 10.1080/21645698.2015.1091553
Chabannes, M. et al. Strong decrease in lignin content without significant alteration of plant development is induced by simultaneous down-regulation of cinnamoyl CoA reductase (CCR) and cinnamyl alcohol dehydrogenase (CAD) in tobacco plants. Plant J. 28, 257–270 (2001).
doi: 10.1046/j.1365-313X.2001.01140.x
Ralph, J. et al. Identification of the structure and origin of a thioacidolysis marker compound for ferulic acid incorporation into angiosperm lignins (and an indicator for cinnamoyl CoA reductase deficiency). Plant J. 53, 368–379 (2008).
doi: 10.1111/j.1365-313X.2007.03345.x
Goujon, T. et al. Down-regulation of the AtCCR1 gene in Arabidopsis thaliana: effects on phenotype, lignins and cell wall degradability. Planta 217, 218–228 (2003).
doi: 10.1007/s00425-003-0987-6
Mir Derikvand, M. et al. Redirection of the phenylpropanoid pathway to feruloyl malate in Arabidopsis mutants deficient for cinnamoyl-CoA reductase 1. Planta 227, 943–956 (2008).
doi: 10.1007/s00425-007-0669-x
Kim, H. et al. Characterization and elimination of undesirable protein residues in plant cell wall materials for enhancing lignin analysis by solution-state nuclear magnetic resonance spectroscopy. Biomacromolecules 18, 4184–4195 (2017).
doi: 10.1021/acs.biomac.7b01223
Van Acker, R. et al. Lignin biosynthesis perturbations affect secondary cell wall composition and saccharification yield in Arabidopsis thaliana. Biotechnol. Biofuels 6, 46 (2013).
doi: 10.1186/1754-6834-6-46
Piquemal, J. et al. Down-regulation of cinnamoyl-CoA reductase induces significant changes of lignin profiles in transgenic tobacco plants. Plant J. 13, 71–83 (1998).
doi: 10.1046/j.1365-313X.1998.00014.x
Chanoca, A., de Vries, L. & Boerjan, W. Lignin engineering in forest trees. Front. Plant Sci. 10, 912 (2019).
doi: 10.3389/fpls.2019.00912
Barrière, Y. Brown-midrib genes in maize and their efficiency in dairy cow feeding. Perspectives for breeding improved silage maize targeting gene modifications in the monolignol and p-hydroxycinnamate pathways. Maydica 62, 1–19 (2017).
Gui, J. et al. Fibre‐specific regulation of lignin biosynthesis improves biomass quality in Populus. N. Phytol. 226, 1074–1087 (2020).
doi: 10.1111/nph.16411
Zhou, X., Jacobs, T. B., Xue, L. J., Harding, S. A. & Tsai, C. J. Exploiting SNPs for biallelic CRISPR mutations in the outcrossing woody perennial Populus reveals 4‐coumarate:CoA ligase specificity and redundancy. N. Phytol. 208, 298–301 (2015).
doi: 10.1111/nph.13470
Xue, L. J., Alabady, M. S., Mohebbi, M. & Tsai, C. J. Exploiting genome variation to improve next-generation sequencing data analysis and genome editing efficiency in Populus tremula × alba 717-1B4. Tree Genet. Genomes 11, 82 (2015).
Jacobs, T. B. & Martin, G. B. High-throughput CRISPR vector construction and characterization of DNA modifications by generation of Tomato hairy roots. J. Vis. Exp. 110, 53843 (2016).
Leplé, J. C., Brasileiro, A. C. M., Michel, M. F., Delmotte, F. & Jouanin, L. Transgenic poplars: expression of chimeric genes using four different constructs. Plant Cell Rep. 11, 137–141 (1992).
doi: 10.1007/BF00232166
Updegraff, D. M. Semimicro determination of cellulose in biological materials. Anal. Biochem. 32, 420–424 (1969).
doi: 10.1016/S0003-2697(69)80009-6
Dence, C. W. in Methods in Lignin Chemistry, Vol. 33–61 (eds Lin, S. Y. & Dence, C. W.) (Springer-Verlag, Berlin, Germany, 1992).
Van den Bosch, S. et al. Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps. Energy Environ. Sci. 8, 1748–1763 (2015).
doi: 10.1039/C5EE00204D
Robinson, A. R. & Mansfield, S. D. Rapid analysis of poplar lignin monomer composition by a streamlined thioacidolysis procedure and near-infrared reflectance-based prediction modeling. Plant J. 58, 706–714 (2009).
doi: 10.1111/j.1365-313X.2009.03808.x
Kim, H. & Ralph, J. Solution-state 2D NMR of ball-milled plant cell wall gels in DMSO-d6/pyridine-d5. Org. Biomolecular Chem. 8, 576–591 (2010).
doi: 10.1039/B916070A
Kim, H. et al. Solution-state 2D NMR of ball-milled plant cell wall gels in DMSO-d6. BioEnergy. Research 1, 56–66 (2008).
Mansfield, S. D. et al. Whole plant cell wall characterization using solution-state 2D-NMR. Nat. Protoc. 7, 1579–1589 (2012).
doi: 10.1038/nprot.2012.064
Van Acker, R., Vanholme, R., Piens, K. & Boerjan, W. Saccharification protocol for small-scale lignocellulosic biomass samples to test processing of cellulose into glucose. Bio-Protoc. 6, e1701 (2016).
doi: 10.21769/BioProtoc.1701
Alberti, S., Gitler, A. D. & Lindquist, S. A suite of Gateway® cloning vectors for high-throughput genetic analysis in Saccharomyces cerevisiae. Yeast 24, 913–919 (2007).
doi: 10.1002/yea.1502
Gietz, R. D. & Woods, R. A. Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method. Methods Enzymol. 350, 87–96 (2002).
doi: 10.1016/S0076-6879(02)50957-5

Auteurs

Barbara De Meester (B)

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052, Ghent, Belgium.
VIB Center for Plant Systems Biology, Technologiepark 71, 9052, Ghent, Belgium.

Barbara Madariaga Calderón (B)

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052, Ghent, Belgium.
VIB Center for Plant Systems Biology, Technologiepark 71, 9052, Ghent, Belgium.

Lisanne de Vries (L)

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052, Ghent, Belgium.
VIB Center for Plant Systems Biology, Technologiepark 71, 9052, Ghent, Belgium.

Jacob Pollier (J)

VIB Metabolomics Core, Technologiepark 71, 9052, Ghent, Belgium.

Geert Goeminne (G)

VIB Metabolomics Core, Technologiepark 71, 9052, Ghent, Belgium.

Jan Van Doorsselaere (J)

Higher Institute for Nursing and Biotechnology, VIVES University College, Wilgenstraat 32, 8800, Roeselare, Belgium.

Mingjie Chen (M)

Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
US Department of Energy, Great Lakes Bioenergy Research Center, Wisconsin Energy Institute, Madison, WI, 53726, USA.

John Ralph (J)

Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
US Department of Energy, Great Lakes Bioenergy Research Center, Wisconsin Energy Institute, Madison, WI, 53726, USA.

Ruben Vanholme (R)

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052, Ghent, Belgium.
VIB Center for Plant Systems Biology, Technologiepark 71, 9052, Ghent, Belgium.

Wout Boerjan (W)

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 71, 9052, Ghent, Belgium. wout.boerjan@psb.vib-ugent.be.
VIB Center for Plant Systems Biology, Technologiepark 71, 9052, Ghent, Belgium. wout.boerjan@psb.vib-ugent.be.

Articles similaires

T-Lymphocytes, Regulatory Lung Neoplasms Proto-Oncogene Proteins p21(ras) Animals Humans

Pathogenic mitochondrial DNA mutations inhibit melanoma metastasis.

Spencer D Shelton, Sara House, Luiza Martins Nascentes Melo et al.
1.00
DNA, Mitochondrial Humans Melanoma Mutation Neoplasm Metastasis
Populus Soil Microbiology Soil Microbiota Fungi
Amaryllidaceae Alkaloids Lycoris NADPH-Ferrihemoprotein Reductase Gene Expression Regulation, Plant Plant Proteins

Classifications MeSH