Evidence map›Paper›PMID 28541580›Full record

ArticleTree physiology2018

Genes and gene clusters related to genotype and drought-induced variation in saccharification potential, lignin content and wood anatomical traits in Populus nigra.

Henning Wildhagen, Shanty Paul, Mike Allwright, Hazel K Smith, Marta Malinowska, Sabine K Schnabel, M João Paulo, Federica Cattonaro, Vera Vendramin, Simone Scalabrin and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Tree physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 45 citations in OpenAlex.

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  17. Engineering Drought Resistance in Forest Trees.Frontiers in plant science · 2018
    Review
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

25 authors at 8 institutions in 6 countries.

Henning WildhagenForest Botany and Tree Physiology, Georg-August University of Goettingen, Büsgenweg 2, 37077 Göttingen, Germany.
Shanty PaulForest Botany and Tree Physiology, Georg-August University of Goettingen, Büsgenweg 2, 37077 Göttingen, Germany.
Mike AllwrightCenter for Biological Sciences, University of Southampton, University Road, Southampton SO17 1BJ, UK.
Hazel K SmithCenter for Biological Sciences, University of Southampton, University Road, Southampton SO17 1BJ, UK.
Marta MalinowskaInstitute of Biological, Environmental & Rural Sciences (IBERS), Aberystwyth University, Gogerddan, Aberystwyth, SY233EE, UK.
Sabine K SchnabelBiometris, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
M João PauloBiometris, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
Federica CattonaroIGA Technology Services, via Jacopo Linussio 51, 33100 Udine, Italy.
Vera VendraminIGA Technology Services, via Jacopo Linussio 51, 33100 Udine, Italy.
Simone ScalabrinIGA Technology Services, via Jacopo Linussio 51, 33100 Udine, Italy.
Dennis JanzForest Botany and Tree Physiology, Georg-August University of Goettingen, Büsgenweg 2, 37077 Göttingen, Germany.
Cyril DoutheUniversidad de les Illes Balears, Carretera de Valldemossa Km 7.5, 07122 Palma de Mallorca, Illes Balears, Spain.
Oliver BrendelEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
Cyril BuréEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
David CohenEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
Irène HummelEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
Didier Le ThiecEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
Fred van EeuwijkBiometris, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
Joost J B KeurentjesLaboratory of Genetics, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
Jaume FlexasUniversidad de les Illes Balears, Carretera de Valldemossa Km 7.5, 07122 Palma de Mallorca, Illes Balears, Spain.
Michele MorganteUniversità Di Udine, Istituto di Genomica Applicata, via Jacopo Linussio 51, 33100 Udine, Italy.
Paul RobsonInstitute of Biological, Environmental & Rural Sciences (IBERS), Aberystwyth University, Gogerddan, Aberystwyth, SY233EE, UK.
Marie-Béatrice Bogeat-TriboulotEEF, INRA, Université de Lorraine, rue d'Amance, 54280 Champenoux, France.
Gail TaylorCenter for Biological Sciences, University of Southampton, University Road, Southampton SO17 1BJ, UK.
Andrea PolleForest Botany and Tree Physiology, Georg-August University of Goettingen, Büsgenweg 2, 37077 Göttingen, Germany.
Université de Lorraine · FRIstituto di Genomica Applicata · ITUniversity of Göttingen · DEWageningen University & Research · NLUniversity of Southampton · GBUniversitat de les Illes Balears · ESAberystwyth University · GBInstitute of Biological, Environmental and Rural Sciences · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/W/00003134A
6 · The paper itself

Abstract

Wood is a renewable resource that can be employed for the production of second generation biofuels by enzymatic saccharification and subsequent fermentation. Knowledge on how the saccharification potential is affected by genotype-related variation of wood traits and drought is scarce. Here, we used three Populus nigra L. genotypes from habitats differing in water availability to (i) investigate the relationships between wood anatomy, lignin content and saccharification and (ii) identify genes and co-expressed gene clusters related to genotype and drought-induced variation in wood traits and saccharification potential. The three poplar genotypes differed in wood anatomy, lignin content and saccharification potential. Drought resulted in reduced cambial activity, decreased vessel and fiber lumina, and increased the saccharification potential. The saccharification potential was unrelated to lignin content as well as to most wood anatomical traits. RNA sequencing of the developing xylem revealed that 1.5% of the analyzed genes were differentially expressed in response to drought, while 67% differed among the genotypes. Weighted gene correlation network analysis identified modules of co-expressed genes correlated with saccharification potential. These modules were enriched in gene ontology terms related to cell wall polysaccharide biosynthesis and modification and vesicle transport, but not to lignin biosynthesis. Among the most strongly saccharification-correlated genes, those with regulatory functions, especially kinases, were prominent. We further identified transcription factors whose transcript abundances differed among genotypes, and which were co-regulated with genes for biosynthesis and modifications of hemicelluloses and pectin. Overall, our study suggests that the regulation of pectin and hemicellulose metabolism is a promising target for improving wood quality of second generation bioenergy crops. The causal relationship of the identified genes and pathways with saccharification potential needs to be validated in further experiments.

Indexed as

DroughtsGenotypeGene ExpressionGenes, PlantHydrolysisLigninMultigene FamilyPolysaccharidesPopulusWoodLigninPolysaccharides

Identifiers

PMID28541580
PMCPMC5982782
OpenAlexW2749395047

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.