Evidence map›Paper›PMID 27679640›Full record

ReviewFrontiers in plant science2016

Methylglyoxal: An Emerging Signaling Molecule in Plant Abiotic Stress Responses and Tolerance.

Tahsina S Hoque, Mohammad A Hossain, Mohammad G Mostofa, David J Burritt, Masayuki Fujita, Lam-Son P Tran

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in plant science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
37.7field-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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 243 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Plants (Basel, Switzerland) · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Genes · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Applied and environmental microbiology · 2024
    Article
  15. Article
  16. Article
  17. The Maize GeneInternational journal of molecular sciences · 2024
    Article
  18. Article
  19. Article
  20. Article

35 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

6 authors at 5 institutions in 4 countries.

Tahsina S HoqueDepartment of Soil Science, Bangladesh Agricultural University Mymensingh, Bangladesh.
Mohammad A HossainDepartment of Genetics and Plant Breeding, Bangladesh Agricultural University Mymensingh, Bangladesh.
Mohammad G MostofaDepartment of Biochemistry and Molecular Biology, Bangabandhu Sheikh Mujibur Rahman Agricultural University Gazipur, Bangladesh.
David J BurrittDepartment of Botany, University of Otago Dunedin, New Zealand.
Masayuki FujitaLaboratory of Plant Stress Responses, Department of Applied Biological Science, Faculty of Agriculture, Kagawa University Kagawa, Japan.
Lam-Son P TranPlant Abiotic Stress Research Group & Faculty of Applied Sciences, Ton Duc Thang UniversityHo Chi Minh City, Vietnam; Signaling Pathway Research Unit, RIKEN Center for Sustainable Resource ScienceYokohama, Japan.
Bangladesh Agricultural University · BDBangabandhu Sheikh Mujibur Rahman Agricultural University · BDKagawa University · JPTon Duc Thang University · VNUniversity of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oxygenated short aldehyde methylglyoxal (MG) is produced in plants as a by-product of a number of metabolic reactions, including elimination of phosphate groups from glycolysis intermediates dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. MG is mostly detoxified by the combined actions of the enzymes glyoxalase I and glyoxalase II that together with glutathione make up the glyoxalase system. Under normal growth conditions, basal levels of MG remain low in plants; however, when plants are exposed to abiotic stress, MG can accumulate to much higher levels. Stress-induced MG functions as a toxic molecule, inhibiting different developmental processes, including seed germination, photosynthesis and root growth, whereas MG, at low levels, acts as an important signaling molecule, involved in regulating diverse events, such as cell proliferation and survival, control of the redox status of cells, and many other aspects of general metabolism and cellular homeostases. MG can modulate plant stress responses by regulating stomatal opening and closure, the production of reactive oxygen species, cytosolic calcium ion concentrations, the activation of inward rectifying potassium channels and the expression of many stress-responsive genes. MG appears to play important roles in signal transduction by transmitting and amplifying cellular signals and functions that promote adaptation of plants growing under adverse environmental conditions. Thus, MG is now considered as a potential biochemical marker for plant abiotic stress tolerance, and is receiving considerable attention by the scientific community. In this review, we will summarize recent findings regarding MG metabolism in plants under abiotic stress, and evaluate the concept of MG signaling. In addition, we will demonstrate the importance of giving consideration to MG metabolism and the glyoxalase system, when investigating plant adaptation and responses to various environmental stresses.

Indexed as

abiotic stressglyoxalasesmethylglyoxalreactive oxygen speciessignaling crosstalkstress tolerance mechanism

Identifiers

PMID27679640
PMCPMC5020096
OpenAlexW2520070183

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.