Evidence map›Paper›PMID 32332750›Full record

ArticleNature communications2020

Methylglyoxal couples metabolic and translational control of Notch signalling in mammalian neural stem cells.

Deivid Carvalho Rodrigues, Emily M Harvey, Rejitha Suraj, Sarah L Erickson, Lamees Mohammad, Mengli Ren, Hongrui Liu, Guiqiong He, David R Kaplan, James Ellis and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. 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
2.1field-weighted citation impact, top 12% 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, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Methylglyoxal Formation-Metabolic Routes and Consequences.Antioxidants (Basel, Switzerland) · 2025
    Review
  7. Article
  8. eLife · 2023
    Article
  9. Metabolites as signalling molecules.Nature reviews. Molecular cell biology · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  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

11 authors at 4 institutions in 2 countries.

Deivid Carvalho RodriguesProgram in Developmental & Stem Cell Biology, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada.
Emily M Harvey *Department of Medical Genetics, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0002-8848-5529
Rejitha Suraj *Department of Medical Genetics, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Sarah L EricksonDepartment of Medical Genetics, University of Calgary, Calgary, AB, T2N 4N1, Canada.ORCID http://orcid.org/0000-0003-3618-5601
Lamees MohammadDepartment of Medical Genetics, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Mengli RenInstitute of Neuroscience, Chongqing Medical University, Chongqing, 400016, China.
Hongrui LiuDepartment of Medical Genetics, University of Calgary, Calgary, AB, T2N 4N1, Canada.
Guiqiong HeInstitute of Neuroscience, Chongqing Medical University, Chongqing, 400016, China.
David R KaplanProgram in Developmental & Stem Cell Biology, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada.
James EllisProgram in Developmental & Stem Cell Biology, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada.ORCID http://orcid.org/0000-0002-4400-0091
Guang YangProgram in Developmental & Stem Cell Biology, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada. guang.yang2@ucalgary.ca.
University of Calgary · CAChongqing Medical University · CNUniversity of Toronto · CAHospital for Sick Children · CA

Funding

CIHR ERT161303CIHR PJT-148746CIHR PJT-165821
6 · The paper itself

Abstract

Gene regulation and metabolism are two fundamental processes that coordinate the self-renewal and differentiation of neural precursor cells (NPCs) in the developing mammalian brain. However, little is known about how metabolic signals instruct gene expression to control NPC homeostasis. Here, we show that methylglyoxal, a glycolytic intermediate metabolite, modulates Notch signalling to regulate NPC fate decision. We find that increased methylglyoxal suppresses the translation of Notch1 receptor mRNA in mouse and human NPCs, which is mediated by binding of the glycolytic enzyme GAPDH to an AU-rich region within Notch1 3'UTR. Interestingly, methylglyoxal inhibits the enzymatic activity of GAPDH and engages it as an RNA-binding protein to suppress Notch1 translation. Reducing GAPDH levels or restoring Notch signalling rescues methylglyoxal-induced NPC depletion and premature differentiation in the developing mouse cortex. Taken together, our data indicates that methylglyoxal couples the metabolic and translational control of Notch signalling to control NPC homeostasis.

Indexed as

Gene Expression Regulation, Developmental3' Untranslated RegionsAnimalsBrainCell DifferentiationCell LineFemaleGlyceraldehyde-3-Phosphate DehydrogenasesHEK293 CellsHumansMiceNeural Stem CellsNeurogenesisProtein BiosynthesisPyruvaldehydeReceptor, Notch13' Untranslated RegionsGlyceraldehyde-3-Phosphate DehydrogenasesNOTCH1 protein, humanNotch1 protein, mousePyruvaldehydeReceptor, Notch1RNA, Messenger

Identifiers

PMID32332750
PMCPMC7181744
OpenAlexW3018878465

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.