Evidence map›Paper›PMID 24201695›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2014

Expression of DNA methyltransferases is influenced by growth hormone in the long-living Ames dwarf mouse in vivo and in vitro.

Vanessa L Armstrong, Sharlene Rakoczy, Lalida Rojanathammanee, Holly M Brown-Borg

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2014. 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
1.6field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  4. Article
  5. The epigenetic aging, obesity, and lifestyle.Frontiers in cell and developmental biology · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Nutritional Epigenomics and Age-Related Disease.Current developments in nutrition · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Revisiting the genomic hypomethylation hypothesis of aging.Annals of the New York Academy of Sciences · 2018
    Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Vanessa L ArmstrongDepartment of Pharmacology, Physiology, and Therapeutics, University of North Dakota School of Medicine and Health Sciences, Grand Forks.
Sharlene RakoczyDepartment of Pharmacology, Physiology, and Therapeutics, University of North Dakota School of Medicine and Health Sciences, Grand Forks.
Lalida RojanathammaneeDepartment of Pharmacology, Physiology, and Therapeutics, University of North Dakota School of Medicine and Health Sciences, Grand Forks.
Holly M Brown-BorgDepartment of Pharmacology, Physiology, and Therapeutics, University of North Dakota School of Medicine and Health Sciences, Grand Forks. holly.brown.borg@med.und.edu.
University of North Dakota · US

Funding

Role of growth hormone in thiol metabolism, stress resistance and agingR01AG034206 · NIA · UNIVERSITY OF NORTH DAKOTA · PI BROWN-BORG, HOLLY M. · 2009 to 2013
$1.4M
Role of GH on thiol metabolism, stress resistance and agingK02AG038509 · NIA · UNIVERSITY OF NORTH DAKOTA · PI BROWN-BORG, HOLLY M. · 2010 to 2014
$575k
NIA NIH HHS K02 AG038509NIA NIH HHS KO2 AG038509NIA NIH HHS R01 AG034206NIA NIH HHS R01AG034206
6 · The paper itself

Abstract

Methyltransferase expression and DNA methylation are linked to aging and age-related disease. We utilized 3-, 12-, and 24-month-old Ames dwarf and their wild-type siblings to examine the genotype and age-related differences in the expression of methyltransferase enzymes related to DNA methylation in the liver, glycine-N-methyltransferase and DNA methyltransferase (DNMT). We found that DNMT proteins and transcripts are differentially expressed in dwarf mice compared with wild-type siblings that can be attributed to age and/or genotype. However, DNMT1 protein expression is drastically reduced compared with wild-type controls at every age. DNMT3a protein levels coincide with differences observed in DNMT activity. Growth hormone appears to modulate expression of DNMT1 and 3a in dwarf liver tissue and primary hepatocytes. Therefore, growth hormone may contribute to age-related processes, DNA methylation, and, ultimately, longevity.

Indexed as

AnimalsColorimetryDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3ADwarfism, PituitaryGlycine N-MethyltransferaseGrowth HormoneHepatocytesImmunoblottingLongevityMethyltransferasesMiceMice, Inbred StrainsRepressor ProteinsDmap1 protein, mouseDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADnmt3a protein, mouseGlycine N-MethyltransferaseGrowth HormoneMethyltransferasesRepressor ProteinsAgingAmes dwarf miceDNA methylationDNA methyltransferaseGlycine-N-methyltransferaseLiver.

Identifiers

PMID24201695
PMCPMC4111294
OpenAlexW2099444594

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.