Evidence map›Paper›PMID 29192139›Full record

ArticleNature communications2017

BEX1 is an RNA-dependent mediator of cardiomyopathy.

Federica Accornero, Tobias G Schips, Jennifer M Petrosino, Shan-Qing Gu, Onur Kanisicak, Jop H van Berlo, Jeffery D Molkentin

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. 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
1.3field-weighted citation impact, top 19% 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, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. RNA binding proteins as mediators of pathological cardiac remodeling.Frontiers in cell and developmental biology · 2024
    Review
  6. Article
  7. Article
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  11. Article
  12. CCN2 participates in overload-induced skeletal muscle hypertrophy.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  13. The mNature communications · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Recurrent rewiring of the adult hippocampal mossy fiber system by a single transcriptional regulator, Id2.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Article
  19. Article
  20. Remodeling of the mJournal of molecular and cellular cardiology · 2021
    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

7 authors at 1 institution in 1 country.

Federica AccorneroCincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA. federica.accornero@osumc.edu.
Tobias G SchipsCincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Jennifer M PetrosinoDorothy M. Davis Heart and Lung Research Institute, Department of Physiology and Cell Biology, Ohio State University, Columbus, OH, 43210, USA.
Shan-Qing GuDorothy M. Davis Heart and Lung Research Institute, Department of Physiology and Cell Biology, Ohio State University, Columbus, OH, 43210, USA.
Onur KanisicakCincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.
Jop H van BerloCincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA.ORCID http://orcid.org/0000-0001-9229-4429
Jeffery D MolkentinCincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA. jeff.molkentin@cchmc.org.
Cincinnati Children's Hospital Medical Center · US

Funding

Post-transcriptional regulation of cardiac hypertrophyR01HL136951 · NHLBI · OHIO STATE UNIVERSITY · PI Federica Accornero · 2017 to 2026
$4.7M
Integrative Training in Biomedical SystemsT32GM068412 · NIGMS · OHIO STATE UNIVERSITY · PI PARVIN, JEFFREY D · 2005 to 2020
$2.4M
BEX1 and the control of protein translation in cardiac hypertrophyR00HL121284 · NHLBI · OHIO STATE UNIVERSITY · PI ACCORNERO, FEDERICA · 2016 to 2018
$727k
Howard Hughes Medical InstituteNHLBI NIH HHS R00 HL121284NHLBI NIH HHS R01 HL136951NIGMS NIH HHS T32 GM068412
6 · The paper itself

Abstract

Regulation of mRNA splicing, processing and stability is increasingly recognized as a critical control point in dynamically altering gene expression during stress or disease. Very little is understood of this process in heart failure. Here, we show that BEX1 is a heart failure-induced gene functioning as an mRNA-associated protein that enhances expression of a subset of cardiac disease-promoting genes. Modeling the increase in BEX1 that occurs in disease, cardiac-specific BEX1 transgenic mice show worse cardiac disease with stress stimulation, whereas Bex1 gene-deleted mice are protected from heart failure-promoting insults. Proteomic and interactive screening assays show that BEX1 is part of a large ribonucleoprotein processing complex involved in regulating proinflammatory mRNA expression in the heart. Specifically, induction of BEX1 augments the stability and expression of AU-rich element containing mRNAs typically found within proinflammatory genes. Thus, BEX1 functions as an mRNA-dependent effector that augments pathology-promoting gene expression during heart failure.

Indexed as

Gene Expression RegulationAnimalsCardiomegalyCardiomyopathiesCase-Control StudiesHeart FailureHumansMiceMice, KnockoutMice, TransgenicNerve Tissue ProteinsProtein Interaction MappingRatsRNA, MessengerRNA SplicingBEX1 protein, humanBex1 protein, mouseNerve Tissue ProteinsRNA, Messenger

Identifiers

PMID29192139
PMCPMC5709413
OpenAlexW2769106524

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.