Evidence map›Paper›PMID 25689854›Full record

ArticlePloS one2015

miR-30 family microRNAs regulate myogenic differentiation and provide negative feedback on the microRNA pathway.

Martin G Guess, Kristen K B Barthel, Brooke C Harrison, Leslie A Leinwand

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  4. Article
  5. Epigenetics of Skeletal Muscle Atrophy.International journal of molecular sciences · 2024
    Review
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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.

Martin G GuessDepartment of Molecular, Cellular and Developmental Biology and BioFrontiers Institute, University of Colorado, Boulder, Colorado, United States of America.
Kristen K B BarthelDepartment of Molecular, Cellular and Developmental Biology and BioFrontiers Institute, University of Colorado, Boulder, Colorado, United States of America.
Brooke C HarrisonDepartment of Molecular, Cellular and Developmental Biology and BioFrontiers Institute, University of Colorado, Boulder, Colorado, United States of America.
Leslie A LeinwandDepartment of Molecular, Cellular and Developmental Biology and BioFrontiers Institute, University of Colorado, Boulder, Colorado, United States of America.
University of Colorado Boulder · US

Funding

MYOSIN GENE DIVERSITY AND FUNCTIONR01GM029090 · NIGMS · YESHIVA UNIVERSITY · PI Leslie Anne Leinwand · 1985 to 2026
$12.3M
POSTGRADUATE TRAINING IN CARDIOVASCULAR RESEARCHT32HL007822 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BUTTRICK, PETER N., LEINWAND, LESLIE ANNE · 1996 to 2023
$6.2M
MOLECULAR BIOLOGYT32GM007135 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI KRAUTER, KENNETH S · 1985 to 2012
$5.7M
MicroRNAs, Muscle Injury, Adaptation, and AgingK01AR055676 · NIAMS · UNIVERSITY OF COLORADO · PI HARRISON, BROOKE · 2010 to 2014
$619k
NHLBI NIH HHS 2T32HL007822-11A2NHLBI NIH HHS T32 HL007822NIAMS NIH HHS K01 AR055676NIAMS NIH HHS K01AR055676NIGMS NIH HHS 5R01GM029090-30NIGMS NIH HHS 5T32GM007135-35NIGMS NIH HHS R01 GM029090NIGMS NIH HHS T32 GM007135
6 · The paper itself

Abstract

microRNAs (miRNAs) are short non-coding RNAs that can mediate changes in gene expression and are required for the formation of skeletal muscle (myogenesis). With the goal of identifying novel miRNA biomarkers of muscle disease, we profiled miRNA expression using miRNA-seq in the gastrocnemius muscles of dystrophic mdx4cv mice. After identifying a down-regulation of the miR-30 family (miR-30a-5p, -30b, -30c, -30d and -30e) when compared to C57Bl/6 (WT) mice, we found that overexpression of miR-30 family miRNAs promotes differentiation, while inhibition restricts differentiation of myoblasts in vitro. Additionally, miR-30 family miRNAs are coordinately down-regulated during in vivo models of muscle injury (barium chloride injection) and muscle disuse atrophy (hindlimb suspension). Using bioinformatics tools and in vitro studies, we identified and validated Smarcd2, Snai2 and Tnrc6a as miR-30 family targets. Interestingly, we show that by targeting Tnrc6a, miR-30 family miRNAs negatively regulate the miRNA pathway and modulate both the activity of muscle-specific miR-206 and the levels of protein synthesis. These findings indicate that the miR-30 family may be an interesting biomarker of perturbed muscle homeostasis and muscle disease.

Indexed as

Feedback, PhysiologicalAnimalsAutoantigensCell DifferentiationChromosomal Proteins, Non-HistoneEpigenesis, GeneticHumansMaleMiceMicroRNAsMuscle DevelopmentMuscle ProteinsMusclesMuscular AtrophySnail Family Transcription FactorsTranscription FactorsAutoantigensChromosomal Proteins, Non-HistoneMicroRNAsMirn30d microRNA, mouseMuscle ProteinsSmarcd2 protein, mouseSNAI2 protein, humanSnai2 protein, mouseSnail Family Transcription FactorsTranscription Factorstrinucleotide repeat containing 6a protein, mouse

Identifiers

PMID25689854
PMCPMC4331529
OpenAlexW1979917340

What OpenQuestion holds

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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.