Evidence map›Paper›PMID 30786857›Full record

ArticleBMC genomics2019

The NAC family transcription factor GmNAC42-1 regulates biosynthesis of the anticancer and neuroprotective glyceollins in soybean.

Md Asraful Jahan, Brianna Harris, Matthew Lowery, Katie Coburn, Aniello M Infante, Ryan J Percifield, Amanda G Ammer, Nik Kovinich

Abstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

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  20. TransgenePlants (Basel, Switzerland) · 2021
    Article
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

8 authors.

Md Asraful JahanDivision of Plant and Soil Sciences, West Virginia University, Morgantown, West Virginia, 26506, USA.
Brianna HarrisDepartment of Biology, West Virginia University, Morgantown, West Virginia, 26506, USA.
Matthew LoweryDepartment of Biochemistry, West Virginia University, Morgantown, West Virginia, 26506, USA.
Katie CoburnDepartment of Biology, West Virginia University, Morgantown, West Virginia, 26506, USA.
Aniello M InfanteDepartment of Biostatistics, West Virginia University, Morgantown, West Virginia, 26506, USA.
Ryan J PercifieldDepartment of Biology, West Virginia University, Morgantown, West Virginia, 26506, USA.
Amanda G AmmerMicroscope Imaging Facility, West Virginia University, Morgantown, West Virginia, 26506, USA.
Nik KovinichDivision of Plant and Soil Sciences, West Virginia University, Morgantown, West Virginia, 26506, USA. Nikola.Kovinich@mail.wvu.edu.ORCID http://orcid.org/0000-0002-9396-6626

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
THE ROLE OF HEF1 PROTEIN IN INVASION OF METASTATIC BREAST CANCERP20RR016440 · NCRR · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2001 to 2010
$22.8M
West Virginia Flow Cytometry Core FacilityP30GM103488 · NIGMS · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2012 to 2016
$4.8M
COBRE FOR SIGNAL TRANSDUCTION AND CANCER PHASE IIIP30RR032138 · NCRR · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2011 to 2011
$1.1M
National Institute of Food and Agriculture 1010200NCRR NIH HHS P20 RR016440NCRR NIH HHS P30 RR032138NIGMS NIH HHS P30 GM103488NIGMS NIH HHS U54 GM104942West Virginia University start-up
6 · The paper itself

Abstract

backgroundGlyceollins are isoflavonoid-derived pathogen-inducible defense metabolites (phytoalexins) from soybean (Glycine max L. Merr) that have important roles in providing defense against pathogens. They also have impressive anticancer and neuroprotective activities in mammals. Despite their potential usefulness as therapeutics, glyceollins are not economical to synthesize and are biosynthesized only transiently and in low amounts in response to specific stresses. Engineering the regulation of glyceollin biosynthesis may be a promising approach to enhance their bioproduction, yet the transcription factors (TFs) that regulate their biosynthesis have remained elusive. To address this, we first aimed to identify novel abiotic stresses that enhance or suppress the elicitation of glyceollins and then used a comparative transcriptomics approach to search for TF gene candidates that may positively regulate glyceollin biosynthesis.

resultsAcidity stress (pH 3.0 medium) and dehydration exerted prolonged (week-long) inductive or suppressive effects on glyceollin biosynthesis, respectively. RNA-seq found that all known biosynthetic genes were oppositely regulated by acidity stress and dehydration, but known isoflavonoid TFs were not. Systemic acquired resistance (SAR) genes were highly enriched in the geneset. We chose to functionally characterize the NAC (NAM/ATAF1/2/CUC2)-family TF GmNAC42-1 that was annotated as an SAR gene and a homolog of the Arabidopsis thaliana (Arabidopsis) indole alkaloid phytoalexin regulator ANAC042. Overexpressing and silencing GmNAC42-1 in elicited soybean hairy roots dramatically enhanced and suppressed the amounts of glyceollin metabolites and biosynthesis gene mRNAs, respectively. Yet, overexpressing GmNAC42-1 in non-elicited hairy roots failed to stimulate the expressions of all biosynthesis genes. Thus, GmNAC42-1 was necessary but not sufficient to activate all biosynthesis genes on its own, suggesting an important role in the glyceollin gene regulatory network (GRN). The GmNAC42-1 protein directly bound the promoters of biosynthesis genes IFS2 and G4DT in the yeast one-hybrid (Y1H) system.

conclusionsAcidity stress is a novel elicitor and dehydration is a suppressor of glyceollin biosynthesis. The TF gene GmNAC42-1 is an essential positive regulator of glyceollin biosynthesis. Overexpressing GmNAC42-1 in hairy roots can be used to increase glyceollin yields > 10-fold upon elicitation. Thus, manipulating the expressions of glyceollin TFs is an effective strategy for enhancing the bioproduction of glyceollins in soybean.

Indexed as

Antineoplastic Agents, PhytogenicBiological TransportGene Expression Regulation, PlantGlycine maxIsoflavonesNeuroprotective AgentsPlant RootsPromoter Regions, GeneticPterocarpansStress, PhysiologicalTranscription FactorsAntineoplastic Agents, PhytogenicglyceollinIsoflavonesNeuroprotective AgentsPterocarpansTranscription FactorsGlyceollinsIsoflavonoidsNACPhytoalexinTranscription factor

Identifiers

PMID30786857
PMCPMC6381636

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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.