Evidence map›Paper›PMID 40583573›Full record

ArticleThe Journal of experimental biology2025

Prolonged fasting and glucocorticoid exposure drive dynamic DNA methylation in northern elephant seals.

Emily F Gibson, Julia María Torres-Velarde, David C Ensminger, Diana D Moreno-Santillán, Daniel E Crocker, José Pablo Vázquez-Medina

Abstract read
In one paragraph

Article in The Journal of experimental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Emily F GibsonDepartment of Integrative Biology, University of California, Berkeley, 3040 Valley Life Sciences Building #3140, Berkeley, CA 94720-3140, USA.
Julia María Torres-VelardeDepartment of Integrative Biology, University of California, Berkeley, 3040 Valley Life Sciences Building #3140, Berkeley, CA 94720-3140, USA.ORCID 0000-0003-3300-2849
David C EnsmingerDepartment of Integrative Biology, University of California, Berkeley, 3040 Valley Life Sciences Building #3140, Berkeley, CA 94720-3140, USA.ORCID 0000-0001-5554-1638
Diana D Moreno-SantillánDepartment of Integrative Biology, University of California, Berkeley, 3040 Valley Life Sciences Building #3140, Berkeley, CA 94720-3140, USA.ORCID 0000-0003-2153-0732
Daniel E CrockerDepartment of Biology, Sonoma State University, Rohnert Park, CA 94928, USA.ORCID 0000-0002-7940-8011
José Pablo Vázquez-MedinaDepartment of Integrative Biology, University of California, Berkeley, 3040 Valley Life Sciences Building #3140, Berkeley, CA 94720-3140, USA.ORCID 0000-0003-1014-5214

Funding

Consejo Nacional de Ciencia y TecnologíasNational Science FoundationUniversity of California BerkeleyUniversity of California, BerkeleyUniversity of California Institute for Mexico and the United States
6 · The paper itself

Abstract

Northern elephant seals experience prolonged fasting while breeding, molting and undergoing postnatal development. Fasting elephant seals adjust neuroendocrine function and gene expression to cope with potentially detrimental effects associated with extended fasting. DNA methylation alters gene expression by modulating accessibility to regions necessary to initiate transcription. The effect of fasting and glucocorticoids on DNA methylation in elephant seals is understudied. We evaluated whether fasting alters global blood DNA methylation, the potential correlation between increased glucocorticoids and methylation, and the effects of glucocorticoids on DNA methylation in cultured northern elephant seal muscle cells. We found that fasting transiently increases blood DNA methylation and that blood DNA methylation levels correlate with plasma cortisol. We then conducted bioinformatic analyses to identify regions in the northern elephant seal glucocorticoid receptor (GR) promoter that influence gene transcription through methylation (CpG islands). We identified one CpG island within the putative GR promoter. Methylation in this region, however, was unaffected by prolonged fasting. We then investigated whether exogenous glucocorticoids alter DNA methylation and gene expression profiles in seal muscle cells in primary culture (myotubes). Exposure to glucocorticoids for 12 or 48 h decreased DNA methylation while upregulating pro-survival gene expression in northern elephant seal muscle cells. Our results show that whereas prolonged fasting transiently increases DNA methylation in northern elephant seal blood, sustained exposure to exogenous glucocorticoids decreases DNA methylation and activates a pro-survival transcriptional program in seal muscle cells. Therefore, our results suggest that DNA methylation is a plastic, potentially cell type-specific response that regulates gene expression in fasting northern elephant seals.

Indexed as

DNA MethylationFastingGlucocorticoidsSeals, EarlessAnimalsCpG IslandsFemaleGene Expression RegulationHydrocortisoneMalePromoter Regions, GeneticReceptors, GlucocorticoidGlucocorticoidsHydrocortisoneReceptors, GlucocorticoidBisulfite sequencingEpigeneticsMarine mammals

Identifiers

PMID40583573
PMCPMC12319411

What Socratic 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 Socratic graph.