Evidence map›Paper›PMID 30980716›Full record

ArticleEndocrinology2019

Glucocorticoid Receptor-Tethered Mineralocorticoid Receptors Increase Glucocorticoid-Induced Transcriptional Responses.

Caroline A Rivers, Mark F Rogers, Felicity E Stubbs, Becky L Conway-Campbell, Stafford L Lightman, John R Pooley

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.5field-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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. The glucocorticoid receptor potentiates aldosterone-induced transcription by the mineralocorticoid receptor.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. The mineralocorticoid receptor forms higher order oligomers upon DNA binding.Protein science : a publication of the Protein Society · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Transcriptional control of energy metabolism by nuclear receptors.Nature reviews. Molecular cell biology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Zebrafish Mutant Lines Reveal the Interplay betweenInternational journal of molecular sciences · 2022
    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

6 authors at 1 institution in 1 country.

Caroline A RiversTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Mark F RogersDepartment of Engineering Mathematics, University of Bristol, Bristol, United Kingdom.
Felicity E StubbsTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Becky L Conway-CampbellTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Stafford L LightmanTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
John R PooleyTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
University of Bristol · GB

Funding

Medical Research Council MR/R010919/1
6 · The paper itself

Abstract

Mineralocorticoid and glucocorticoid receptors (MRs and GRs) constitute a functionally important dual receptor system detecting and transmitting circulating corticosteroid signals. High expression of MRs and GRs occurs in the same cells in the limbic system, the primary site of glucocorticoid action on cognition, behavior, and mood; however, modes of interaction between the receptors are poorly characterized. We used chromatin immunoprecipitation with nucleotide resolution using exonuclease digestion, unique barcode, and single ligation (ChIP-nexus) for high-resolution genome-wide characterization of MR and GR DNA binding profiles in neuroblastoma cells and demonstrate recruitment to highly similar DNA binding sites. Expressed MR or GR showed differential regulation of endogenous gene targets, including Syt2 and Ddc, whereas coexpression produced augmented transcriptional responses even when MRs were unable to bind DNA (MR-XDBD). ChIP confirmed that MR-XDBD could be tethered to chromatin by GR. Our data demonstrate that MR can interact at individual genomic DNA sites in multiple modes and suggest a role for MR in increasing the transcriptional response to glucocorticoids.

Indexed as

AnimalsBase SequenceBinding SitesCell Line, TumorChromatin ImmunoprecipitationDNAGlucocorticoidsMiceProtein BindingRatsReceptors, GlucocorticoidReceptors, MineralocorticoidResponse ElementsRNA InterferenceTranscription, GeneticDNAGlucocorticoidsReceptors, GlucocorticoidReceptors, Mineralocorticoid

Identifiers

PMID30980716
PMCPMC6462215
OpenAlexW2921539299

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.