Evidence map›Paper›PMID 30919132›Full record

ArticleProtoplasma2019

SlNAC2 overexpression in Arabidopsis results in enhanced abiotic stress tolerance with alteration in glutathione metabolism.

Pankaj Borgohain, Bedabrata Saha, Rajkishan Agrahari, Bhaben Chowardhara, Smita Sahoo, Christell van der Vyver, Sanjib Kumar Panda

Abstract read
PubMed Publisher
In one paragraph

Article in Protoplasma, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
8.1field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
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  7. Review
  8. Review
  9. Plants (Basel, Switzerland) · 2022
    Article
  10. A Transcription FactorInternational journal of molecular sciences · 2022
    Article
  11. Over-Expression of an R2R3 MYB Gene,International journal of molecular sciences · 2022
    Article
  12. Article
  13. ThePhysiology and molecular biology of plants : an international journal of functional plant biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

7 authors at 2 institutions in 2 countries.

Pankaj BorgohainPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India.
Bedabrata SahaPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India.
Rajkishan AgrahariPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India.
Bhaben ChowardharaPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India.
Smita SahooPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India.
Christell van der VyverInstitute for Plant Biotechnology, Department of Genetics, University of Stellenbosch, Stellenbosch, 7602, South Africa.
Sanjib Kumar PandaPlant Functional Genomics Laboratory, Department of Life Science and Bioinformatics, Assam University, Silchar, 788011, India. drskpanda@gmail.com.
Assam University · INStellenbosch University · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant NAC (NAM, ATAF, and CUC) transcription factors (TF) have important roles to play in abiotic stress responses through activation of a battery of functional genes/transcriptional regulators responsible for stress tolerance. Here we report the cloning of a novel Solanum lycopersicum L., NAC2 TF having 960 nucleotides long CDS (GenBank: KT740994.1). Phylogenetic analysis depicted the similarity of SlNAC2 to other orthologs. SlNAC2 was overexpressed in Arabidopsis thaliana to assess and characterize its role in plant abiotic stress responses. The transgenic events were first confirmed by genomic DNA PCR and qRT PCR; then the T3 generation plants were used for stress assays. Soil stress assay depicted better survivability of the transgenic plants under both salt (NaCl) and drought (PEG) stress. The transgenic plants showed enhanced endurance; with better antioxidative response, reduced accumulation of reactive oxygen species (ROS) molecules and better retention of water in tissue. This study for the very first time analyzed the different stakeholders of the glutathione metabolism in SlNAC2 overexpressing transgenic lines on exposure to both salinity and PEG stress. The expression of the two genes (ɤ-ECS, GS) responsible for glutathione biosynthesis increased with SlNAC2 overexpression. Further glutathione reductase responsible for reduction of glutathione disulfide (GSSG) to glutathione (GSH) also increased significantly which suggested the regulation of glutathione metabolism as a mechanism for the osmotic stress tolerance conferred to plants upon NAC overexpression.

Indexed as

AntioxidantsArabidopsisChlorophyllCloning, MolecularDroughtsEnzymesGene Expression Regulation, PlantGlutathioneMalondialdehydeOxidative StressPhylogenyPlant ProteinsPlants, Genetically ModifiedSalt StressSolanum lycopersicumStress, PhysiologicalAntioxidantsChlorophyllEnzymesGlutathioneMalondialdehydePlant ProteinsTranscription FactorsAbiotic stressArabidopsis thalianaDroughtGlutathioneNACSalinityTomato

Identifiers

PMID30919132
OpenAlexW2922636182

What OpenQuestion holds

Textmetadata
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.