Evidence map›Paper›PMID 27422824›Full record

ArticleThe Journal of biological chemistry2016

Phosphorylation of Mineralocorticoid Receptor Ligand Binding Domain Impairs Receptor Activation and Has a Dominant Negative Effect over Non-phosphorylated Receptors.

Rubén Jiménez-Canino, Miguel X Fernandes, Diego Alvarez de la Rosa

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. 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
  2. The mineralocorticoid receptor forms higher order oligomers upon DNA binding.Protein science : a publication of the Protein Society · 2024
    Article
  3. Article
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  7. Review
  8. Review
  9. Mineralocorticoid receptor as a therapeutic target in chronic kidney disease and hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2017
    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

3 authors at 1 institution in 1 country.

Rubén Jiménez-CaninoFrom the Departamento de Ciencias Médicas Básicas, Instituto de Tecnologías Biomédicas y Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, 38071 La Laguna, Tenerife, Spain.
Miguel X FernandesFrom the Departamento de Ciencias Médicas Básicas, Instituto de Tecnologías Biomédicas y Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, 38071 La Laguna, Tenerife, Spain.
Diego Alvarez de la RosaFrom the Departamento de Ciencias Médicas Básicas, Instituto de Tecnologías Biomédicas y Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, 38071 La Laguna, Tenerife, Spain diego.alvarez@ull.edu.es.ORCID 0000-0002-4324-2793
Universidad de La Laguna · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-translational modification of steroid receptors allows fine-tuning different properties of this family of proteins, including stability, activation, or interaction with co-regulators. Recently, a novel effect of phosphorylation on steroid receptor biology was described. Phosphorylation of human mineralocorticoid receptor (MR) on Ser-843, a residue placed on the ligand binding domain, lowers affinity for agonists, producing inhibition of gene transactivation. We now show that MR inhibition by phosphorylation occurs even at high agonist concentration, suggesting that phosphorylation may also impair coupling between ligand binding and receptor activation. Our results demonstrate that agonists are able to induce partial nuclear translocation of MR but fail to produce transactivation due at least in part to impaired co-activator recruitment. The inhibitory effect of phosphorylation on MR acts in a dominant-negative manner, effectively amplifying its functional effect on gene transactivation.

Indexed as

Active Transport, Cell NucleusAmino Acid SubstitutionAnimalsCell NucleusChlorocebus aethiopsCOS CellsHumansMiceMutation, MissensePhosphorylationProtein BindingReceptors, MineralocorticoidTranscriptional ActivationReceptors, Mineralocorticoidaldosteronecortisolgene transcriptionglucocorticoid receptorkidneymineralocorticoid receptorphosphorylationsteroid hormone receptor

Identifiers

PMID27422824
PMCPMC5009277
OpenAlexW2464252422

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.