Evidence map›Paper›PMID 26093023›Full record

ArticleJournal of experimental botany2015

Effects of PHENYLALANINE AMMONIA LYASE (PAL) knockdown on cell wall composition, biomass digestibility, and biotic and abiotic stress responses in Brachypodium.

Cynthia L Cass, Antoine Peraldi, Patrick F Dowd, Yaseen Mottiar, Nicholas Santoro, Steven D Karlen, Yury V Bukhman, Cliff E Foster, Nick Thrower, Laura C Bruno and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of experimental botany, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

89 citing papers in PubMed, 1 synthesis or guideline pooled it, 217 citations in OpenAlex.

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29 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 7 institutions in 3 countries.

Cynthia L CassSchool of Biological Sciences, Illinois State University, Normal, IL 61790 USA US Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
Antoine PeraldiDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Patrick F DowdUSDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Crop Bioprotection Research Unit, Peoria, IL 61604, USA.
Yaseen MottiarUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA Department of Wood Science, University of British Columbia, Vancouver, V6T 1Z4, Canada.
Nicholas SantoroUS Department of Energy Great Lakes Bioenergy Research Center, Michigan State University, East Lansing, MI 48824, USA.
Steven D KarlenUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
Yury V BukhmanUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
Cliff E FosterUS Department of Energy Great Lakes Bioenergy Research Center, Michigan State University, East Lansing, MI 48824, USA.
Nick ThrowerUS Department of Energy Great Lakes Bioenergy Research Center, Michigan State University, East Lansing, MI 48824, USA.
Laura C BrunoDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Oleg V MoskvinUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
Eric T JohnsonUSDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Crop Bioprotection Research Unit, Peoria, IL 61604, USA.
Megan E WillhoitSchool of Biological Sciences, Illinois State University, Normal, IL 61790 USA US Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
Megha PhutaneSchool of Biological Sciences, Illinois State University, Normal, IL 61790 USA US Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA.
John RalphUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA Department of Biochemistry, Wisconsin Energy Institute, University of Wisconsin, Madison, WI 53706, USA.
Shawn D MansfieldUS Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA Department of Wood Science, University of British Columbia, Vancouver, V6T 1Z4, Canada.
Paul NicholsonDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
John C SedbrookSchool of Biological Sciences, Illinois State University, Normal, IL 61790 USA US Department of Energy Great Lakes Bioenergy Research Center, Madison, WI 53706, USA jcsedbr@ilstu.edu.
Great Lakes Bioenergy Research Center · USIllinois State University · USJohn Innes Centre · GBMichigan State University · USNational Center for Agricultural Utilization Research · USNorwich Research Park · GBUniversity of Wisconsin–Madison · US

Funding

Biotechnology and Biological Sciences Research Council BBS/E/J/00000606
6 · The paper itself

Abstract

The phenylpropanoid pathway in plants synthesizes a variety of structural and defence compounds, and is an important target in efforts to reduce cell wall lignin for improved biomass conversion to biofuels. Little is known concerning the trade-offs in grasses when perturbing the function of the first gene family in the pathway, PHENYLALANINE AMMONIA LYASE (PAL). Therefore, PAL isoforms in the model grass Brachypodium distachyon were targeted, by RNA interference (RNAi), and large reductions (up to 85%) in stem tissue transcript abundance for two of the eight putative BdPAL genes were identified. The cell walls of stems of BdPAL-knockdown plants had reductions of 43% in lignin and 57% in cell wall-bound ferulate, and a nearly 2-fold increase in the amounts of polysaccharide-derived carbohydrates released by thermochemical and hydrolytic enzymic partial digestion. PAL-knockdown plants exhibited delayed development and reduced root growth, along with increased susceptibilities to the fungal pathogens Fusarium culmorum and Magnaporthe oryzae. Surprisingly, these plants generally had wild-type (WT) resistances to caterpillar herbivory, drought, and ultraviolet light. RNA sequencing analyses revealed that the expression of genes associated with stress responses including ethylene biosynthesis and signalling were significantly altered in PAL knocked-down plants under non-challenging conditions. These data reveal that, although an attenuation of the phenylpropanoid pathway increases carbohydrate availability for biofuel, it can adversely affect plant growth and disease resistance to fungal pathogens. The data identify notable differences between the stress responses of these monocot pal mutants versus Arabidopsis (a dicot) pal mutants and provide insights into the challenges that may arise when deploying phenylpropanoid pathway-altered bioenergy crops.

Indexed as

BiomassStress, PhysiologicalBrachypodiumPhenylalanine Ammonia-LyasePhenylalanine Ammonia-LyaseBioenergyferulic acidFusariumgrassherbivoryligninphenylpropanoidsaccharificationtyrosine ammonia lyaseultraviolet light.

Identifiers

PMID26093023
PMCPMC4493789
OpenAlexW2127335219

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.