Evidence map›Paper›PMID 26160899›Full record

ArticleDevelopment (Cambridge, England)2015

Endothelin signaling activates Mef2c expression in the neural crest through a MEF2C-dependent positive-feedback transcriptional pathway.

Jianxin Hu, Michael P Verzi, Ashley S Robinson, Paul Ling-Fung Tang, Lisa L Hua, Shan-Mei Xu, Pui-Yan Kwok, Brian L Black

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Endothelin signaling in development.Development (Cambridge, England) · 2023
    Review
  5. Biomolecules · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. A CRISPR Path to Engineering New Genetic Mouse Models for Cardiovascular Research.Arteriosclerosis, thrombosis, and vascular biology · 2016
    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

8 authors at 1 institution in 1 country.

Jianxin HuCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Michael P VerziCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Ashley S RobinsonCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Paul Ling-Fung TangCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Lisa L HuaCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Shan-Mei XuCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA.
Pui-Yan KwokCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA Department of Dermatology, University of California, San Francisco, CA 94143, USA.
Brian L BlackCardiovascular Research Institute, University of California, San Francisco, CA 94143, USA Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94143, USA brian.black@ucsf.edu.
University of California, San Francisco · US

Funding

Transcriptional Networks During Cardiac DifferentiationP01HL089707 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI SRIVASTAVA, DEEPAK · 2008 to 2017
$20.4M
Regulation of cardiovascular transcriptionR01HL064658 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLACK, BRIAN L · 2000 to 2019
$5.4M
Molecular and Genetic Regulation of Craniofacial DevelopmentR01DE019118 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLACK, BRIAN L · 2009 to 2013
$1.9M
NHLBI NIH HHS HL064658NHLBI NIH HHS HL089707NHLBI NIH HHS P01 HL089707NHLBI NIH HHS R01 HL064658NIDCR NIH HHS DE019118NIDCR NIH HHS R01 DE019118
6 · The paper itself

Abstract

Endothelin signaling is essential for neural crest development, and dysregulated Endothelin signaling is associated with several neural crest-related disorders, including Waardenburg and other syndromes. However, despite the crucial roles of this pathway in neural crest development and disease, the transcriptional effectors directly activated by Endothelin signaling during neural crest development remain incompletely elucidated. Here, we establish that the MADS box transcription factor MEF2C is an immediate downstream transcriptional target and effector of Endothelin signaling in the neural crest. We show that Endothelin signaling activates Mef2c expression in the neural crest through a conserved enhancer in the Mef2c locus and that CRISPR-mediated deletion of this Mef2c neural crest enhancer from the mouse genome abolishes Endothelin induction of Mef2c expression. Moreover, we demonstrate that Endothelin signaling activates neural crest expression of Mef2c by de-repressing MEF2C activity through a Calmodulin-CamKII-histone deacetylase signaling cascade. Thus, these findings identify a MEF2C-dependent, positive-feedback mechanism for Endothelin induction and establish MEF2C as an immediate transcriptional effector and target of Endothelin signaling in the neural crest.

Indexed as

Animalsbeta-GalactosidaseEndothelinsFeedback, PhysiologicalGalactosidesGene Expression Regulation, DevelopmentalIndolesIn Situ HybridizationMEF2 Transcription FactorsMiceMice, TransgenicNeural CrestSignal Transduction5-bromo-4-chloro-3-indolyl beta-galactosidebeta-GalactosidaseEndothelinsGalactosidesIndolesMef2c protein, mouseMEF2 Transcription FactorsCraniofacial developmentEndothelinMEF2CMelanocytesMouseNeural crestTranscription

Identifiers

PMID26160899
PMCPMC4550968
OpenAlexW1773548472

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.