Evidence map›Paper›PMID 24634509›Full record

ArticleJournal of cell science2014

MicroRNA-30a regulates zebrafish myogenesis through targeting the transcription factor Six1.

Jenean H O'Brien, Laura Hernandez-Lagunas, Kristin Bruk Artinger, Heide L Ford

Abstract read
In one paragraph

Article in Journal of cell science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. MiR-202-3p determines embryo viability during mid-blastula transition.Frontiers in cell and developmental biology · 2022
    Article
  6. Transcriptomic Analysis Provides Insights to Reveal theFrontiers in cell and developmental biology · 2022
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. LncRNA-Six1 Encodes a Micropeptide to ActivateFrontiers in physiology · 2017
    Article
  15. Review
  16. Article
  17. 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

4 authors at 1 institution in 1 country.

Jenean H O'BrienDepartment of Pharmacology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Laura Hernandez-LagunasDepartment of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Kristin Bruk ArtingerDepartment of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA Kristin.Artinger@ucdenver.edu Heide.Ford@ucdenver.edu.
Heide L FordDepartment of Pharmacology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA Kristin.Artinger@ucdenver.edu Heide.Ford@ucdenver.edu.
University of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Role of Six1 in EMT and Tumor ProgressionR01CA095277 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L. · 2002 to 2017
$4.3M
Regulation and function of Six1 in zebrafish muscle development and in rhabdomyosF32CA174169 · NCI · UNIVERSITY OF COLORADO DENVER · PI O'BRIEN, JENEAN · 2013 to 2015
$165k
NCI NIH HHS F32 CA174169NCI NIH HHS F32CA174169NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA095277NCI NIH HHS R01CA095277
6 · The paper itself

Abstract

Precise spatiotemporal regulation of the SIX1 homeoprotein is required to coordinate vital tissue development, including myogenesis. Whereas SIX1 is downregulated in most tissues following embryogenesis, it is re-expressed in numerous cancers, including tumors derived from muscle progenitors. Despite crucial roles in development and disease, the upstream regulation of SIX1 expression has remained elusive. Here, we identify the first direct mechanism for Six1 regulation in embryogenesis, through microRNA30a (miR30a)-mediated repression. In zebrafish somites, we show that miR30a and six1a and six1b (hereafter six1a/b) are expressed in an inverse temporal pattern. Overexpression of miR30a leads to a reduction in six1a/b levels, and results in increased apoptosis and altered somite morphology, which phenocopies six1a/b knockdown. Conversely, miR30a inhibition leads to increased Six1 expression and abnormal somite morphology, revealing a role for endogenous miR30a as a muscle-specific miRNA (myomiR). Importantly, restoration of six1a in miR30a-overexpressing embryos restores proper myogenesis. These data demonstrate a new role for miR30a at a key node in the myogenic regulatory gene network through controlling Six1 expression.

Indexed as

AnimalsCell DifferentiationCell ProliferationGene Expression Regulation, DevelopmentalGene Knockdown TechniquesGene Regulatory NetworksHomeodomain ProteinsMicroRNAsMuscle DevelopmentZebrafishZebrafish ProteinsHomeodomain ProteinsMicroRNAsMIRN30 microRNA, zebrafishSix1 protein, zebrafishZebrafish ProteinsmicroRNA-30aMyogenesisSix1Zebrafish

Identifiers

PMID24634509
PMCPMC4021474
OpenAlexW2032791246

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.