Evidence map›Paper›PMID 26335593›Full record

ArticleBMC plant biology2015

Implications of ethylene biosynthesis and signaling in soybean drought stress tolerance.

Fabricio Barbosa Monteiro Arraes, Magda Aparecida Beneventi, Maria Eugenia Lisei de Sa, Joaquin Felipe Roca Paixao, Erika Valeria Saliba Albuquerque, Silvana Regina Rockenbach Marin, Eduardo Purgatto, Alexandre Lima Nepomuceno, Maria Fatima Grossi-de-Sa

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
16.6field-weighted citation impact, top 1% 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

70 citing papers in PubMed, 168 citations in OpenAlex.

  1. Article
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  8. Elevated COThe New phytologist · 2025
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  9. Ethylene Signaling Modulates Dehydrin Expression inInternational journal of molecular sciences · 2025
    Article
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  12. Improved Protocol for EfficientPlants (Basel, Switzerland) · 2024
    Article
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10 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

9 authors at 2 institutions in 1 country.

Fabricio Barbosa Monteiro ArraesFederal University of Rio Grande do Sul, Campus do Vale, Av. Bento Gonçalves 9500, Postal Code 15005, CEP 91501-970, Porto Alegre, RS, Brazil. fabricio.arraes@gmail.com.
Magda Aparecida BeneventiFederal University of Rio Grande do Sul, Campus do Vale, Av. Bento Gonçalves 9500, Postal Code 15005, CEP 91501-970, Porto Alegre, RS, Brazil. magbeneventi@gmail.com.
Maria Eugenia Lisei de SaEmbrapa Genetic Resources and Biotechnology, PqEB, Av. W5-Norte, Postal Code 02372, CEP 70770-910, Brasilia, DF, Brazil. maria-eugenia.sa@colaborador.embrapa.br.
Joaquin Felipe Roca PaixaoEmbrapa Genetic Resources and Biotechnology, PqEB, Av. W5-Norte, Postal Code 02372, CEP 70770-910, Brasilia, DF, Brazil. joaquinfrp@gmail.com.
Erika Valeria Saliba AlbuquerqueEmbrapa Genetic Resources and Biotechnology, PqEB, Av. W5-Norte, Postal Code 02372, CEP 70770-910, Brasilia, DF, Brazil. erika.albuquerque@embrapa.br.
Silvana Regina Rockenbach MarinEmbrapa Soybean, Rodovia Carlos João Strass, SN, Acesso Orlando Amaral, Distrito de Warta, Postal Code 231, CEP 86001-970, Londrina, PR, Brazil. silvana.marin@embrapa.br.
Eduardo PurgattoFood Chemistry and Biochemistry Laboratory, Sao Paulo University, Av. Lineu Prestes 580, Bloco 14, Cidade Universitaria, CEP 05508-000, Sao Paulo, SP, Brazil. epurgatt@usp.br.
Alexandre Lima NepomucenoEmbrapa Soybean, Rodovia Carlos João Strass, SN, Acesso Orlando Amaral, Distrito de Warta, Postal Code 231, CEP 86001-970, Londrina, PR, Brazil. alexandre.nepomuceno@embrapa.br.
Maria Fatima Grossi-de-SaEmbrapa Genetic Resources and Biotechnology, PqEB, Av. W5-Norte, Postal Code 02372, CEP 70770-910, Brasilia, DF, Brazil. fatima.grossi@embrapa.br.
Brazilian Agricultural Research Corporation · BRUniversidade Federal do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEthylene is a phytohormone known for inducing a triple response in seedlings, leaf abscission and other responses to various stresses. Several studies in model plants have evaluated the importance of this hormone in crosstalk signaling with different metabolic pathways, in addition to responses to biotic stresses. However, the mechanism of action in plants of agricultural interest, such as soybean, and its participation in abiotic stresses remain unclear.

resultsThe studies presented in this work allowed for the identification of 176 soybean genes described elsewhere for ethylene biosynthesis (108 genes) and signal transduction (68 genes). A model to predict these routes in soybean was proposed, and it had great representability compared to those described for Arabidopsis thaliana and Oryza sativa. Furthermore, analysis of putative gene promoters from soybean gene orthologs permitted the identification of 29 families of cis-acting elements. These elements are essential for ethylene-mediated regulation and its possible crosstalk with other signaling pathways mediated by other plant hormones. From genes that are differentially expressed in the transcriptome database, we analyzed the relative expression of some selected genes in resistant and tolerant soybean plants subjected to water deficit. The differential expression of a set of five soybean ethylene-related genes (MAT, ACS, ACO, ETR and CTR) was validated with RT-qPCR experiments, which confirmed variations in the expression of these soybean target genes, as identified in the transcriptome database. In particular, two families of ethylene biosynthesis genes (ACS and ACO) were upregulated under these experimental conditions, whereas CTR (involved in ethylene signal transduction) was downregulated. In the same samples, high levels of ethylene production were detected and were directly correlated with the free fraction levels of ethylene's precursor. Thus, the combination of these data indicated the involvement of ethylene biosynthesis and signaling in soybean responses to water stress.

conclusionsThe in silico analysis, combined with the quantification of ethylene production (and its precursor) and RT-qPCR experiments, allowed for a better understanding of the importance of ethylene at a molecular level in this crop as well as its role in the response to abiotic stresses. In summary, all of the data presented here suggested that soybean responses to water stress could be regulated by a crosstalk network among different signaling pathways, which might involve various phytohormones, such as auxins, ABA and jasmonic acid. The integration of in silico and physiological data could also contribute to the application of biotechnological strategies to the development of improved cultivars with regard to different stresses, such as the isolation of stress-specific plant promoters.

Indexed as

DroughtsGene Expression Regulation, PlantComputer SimulationEthylenesGlycine maxMetabolic Networks and PathwaysModels, GeneticPlant Growth RegulatorsSignal TransductionStress, PhysiologicalTranscriptomeethyleneEthylenesPlant Growth Regulators

Identifiers

PMID26335593
PMCPMC4557918
OpenAlexW2169004866

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LicenceCC BY
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Registered trials

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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.