Evidence map›Paper›PMID 26924399›Full record

ArticleBiochimie2016

Formate supplementation enhances folate-dependent nucleotide biosynthesis and prevents spina bifida in a mouse model of folic acid-resistant neural tube defects.

Sonia Sudiwala, Sandra C P De Castro, Kit-Yi Leung, John T Brosnan, Margaret E Brosnan, Kevin Mills, Andrew J Copp, Nicholas D E Greene

Open access · hybridAbstract read
In one paragraph

Article in Biochimie, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Acidity induces durable enhancement of TMolecular immunology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Formate metabolism in health and disease.Molecular metabolism · 2020
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Deletion of the neural tube defect-associated geneThe Journal of biological chemistry · 2018
    Article
  13. Observational
  14. Article
  15. Review
  16. 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 at 3 institutions in 2 countries.

Sonia SudiwalaNewlife Birth Defects Research Centre and Developmental Biology & Cancer Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK.
Sandra C P De CastroNewlife Birth Defects Research Centre and Developmental Biology & Cancer Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK.
Kit-Yi LeungNewlife Birth Defects Research Centre and Developmental Biology & Cancer Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK.
John T BrosnanDepartment of Biochemistry, Memorial University of Newfoundland, St John's, NL, A1B3X9, Canada.
Margaret E BrosnanDepartment of Biochemistry, Memorial University of Newfoundland, St John's, NL, A1B3X9, Canada.
Kevin MillsGenetics & Genomic Medicine Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK.
Andrew J CoppNewlife Birth Defects Research Centre and Developmental Biology & Cancer Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK.
Nicholas D E GreeneNewlife Birth Defects Research Centre and Developmental Biology & Cancer Programme, Institute of Child Health, University College London, London, WC1N 1EH, UK. Electronic address: n.greene@ucl.ac.uk.
University College London · GBMemorial University of Newfoundland · CACancer Research UK · GB

Funding

Medical Research Council J003794Medical Research Council MR/J003794/1Medical Research Council MR/N003713/1Wellcome Trust 087525
6 · The paper itself

Abstract

The curly tail mouse provides a model for neural tube defects (spina bifida and exencephaly) that are resistant to prevention by folic acid. The major ct gene, responsible for spina bifida, corresponds to a hypomorphic allele of grainyhead-like 3 (Grhl3) but the frequency of NTDs is strongly influenced by modifiers in the genetic background. Moreover, exencephaly in the curly tail strain is not prevented by reinstatement of Grhl3 expression. In the current study we found that expression of Mthfd1L, encoding a key component of mitochondrial folate one-carbon metabolism (FOCM), is significantly reduced in ct/ct embryos compared to a partially congenic wild-type strain. This expression change is not attributable to regulation by Grhl3 or the genetic background at the Mthfd1L locus. Mitochondrial FOCM provides one-carbon units as formate for FOCM reactions in the cytosol. We found that maternal supplementation with formate prevented NTDs in curly tail embryos and also resulted in increased litter size. Analysis of the folate profile of neurulation-stage embryos showed that formate supplementation resulted in an increased proportion of formyl-THF and THF but a reduction in proportion of 5-methyl THF. In contrast, THF decreased and 5-methyl THF was relatively more abundant in the liver of supplemented dams than in controls. In embryos cultured through the period of spinal neurulation, incorporation of labelled thymidine and adenine into genomic DNA was suppressed by supplemental formate, suggesting that de novo folate-dependent biosynthesis of nucleotides (thymidylate and purines) was enhanced. We hypothesise that reduced Mthfd1L expression may contribute to susceptibility to NTDs in the curly tail strain and that formate acts as a one-carbon donor to prevent NTDs.

Indexed as

Spinal DysraphismAnimalsDisease Models, AnimalFolic AcidFormatesMiceNucleotidesFolic AcidFormatesformic acidNucleotidesFolate one-carbon metabolismFolic acidFormateGrainyhead-like 3mthfd1LNeural tube defects

Identifiers

PMID26924399
PMCPMC4909716
OpenAlexW2275626939

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.