Evidence map›Paper›PMID 30467785›Full record

ArticleMarine biotechnology (New York, N.Y.)2019

Genetic Mutations in jamb, jamc, and myomaker Revealed Different Roles on Myoblast Fusion and Muscle Growth.

Yufeng Si, Haishen Wen, Shaojun Du

Open access · greenAbstract read
In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. The Pattern of Gene Expression (Animals : an open access journal from MDPI · 2024
    Article
  4. Article
  5. The Regulatory Role ofAnimals : an open access journal from MDPI · 2024
    Article
  6. Molecular regulation of myocyte fusion.Current topics in developmental biology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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 2 institutions in 2 countries.

Yufeng SiDepartment of Biochemistry and Molecular Biology, Institute of Marine and Environmental Technology, University of Maryland School of Medicine, 701 East Pratt Street, Baltimore, MD, 21202, USA.
Haishen WenThe Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao, 266003, China.
Shaojun DuDepartment of Biochemistry and Molecular Biology, Institute of Marine and Environmental Technology, University of Maryland School of Medicine, 701 East Pratt Street, Baltimore, MD, 21202, USA. sdu@som.umaryland.edu.ORCID http://orcid.org/0000-0001-9227-4153
University of Maryland, Baltimore · USOcean University of China · CN

Funding

Molecular regulation of muscle development by Smyd1R01AR072703 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI DU, SHAOJUN · 2018 to 2023
$1.7M
National Institute of Health (USA) 1R01AR072703-01A1NIAMS NIH HHS R01 AR072703
6 · The paper itself

Abstract

Myoblast fusion is a vital step for skeletal muscle development, growth, and regeneration. Loss of Jamb, Jamc, or Myomaker (Mymk) function impaired myoblast fusion in zebrafish embryos. In addition, mymk mutation hampered fish muscle growth. However, the effect of Jamb and Jamc deficiency on fish muscle growth is not clear. Moreover, whether jamb;jamc and jamb;mymk double mutations have stronger effects on myoblast fusion and muscle growth remains to be investigated. Here, we characterized the muscle development and growth in jamb, jamc, and mymk single and double mutants in zebrafish. We found that although myoblast fusion was compromised in jamb and jamc single or jamb;jamc double mutants, these mutant fish showed no defect in muscle cell fusion during muscle growth. The mutant fish were able to grow into adults that were indistinguishable from the wild-type sibling. In contrast, the jamb;mymk double mutants exhibited a stronger muscle phenotype compared to the jamb and jamc single and double mutants. The jamb;mymk double mutant showed reduced growth and partial lethality, similar to a mymk single mutant. Single fiber analysis of adult skeletal myofibers revealed that jamb, jamc, or jamb;jamc mutants contained mainly multinucleated myofibers, whereas jamb;mymk double mutants contained mostly mononucleated fibers. Significant intramuscular adipocyte infiltration was found in skeletal muscles of the jamb;mymk mutant. Collectively, these studies demonstrate that although Jamb, Jamc, and Mymk are all involved in myoblast fusion during early myogenesis, they have distinct roles in myoblast fusion during muscle growth. While Mymk is essential for myoblast fusion during both muscle development and growth, Jamb and Jamc are dispensable for myoblast fusion during muscle growth.

Indexed as

AnimalsAnimals, Genetically ModifiedCell CommunicationCell DifferentiationCell FusionEmbryo, NonmammalianGene Expression Regulation, DevelopmentalJunctional Adhesion Molecule BMembrane ProteinsMuscle DevelopmentMuscle Fibers, SkeletalMuscle ProteinsMuscle, SkeletalMutationMyoblastsReceptors, Cell SurfaceJam2a protein, zebrafishJam3b protein, zebrafishJunctional Adhesion Molecule BMembrane ProteinsMuscle Proteinsmymk protein, zebrafishReceptors, Cell SurfaceZebrafish ProteinsJambJamcMuscle fusionMyomakerZebrafish

Identifiers

PMID30467785
PMCPMC6467518
OpenAlexW2901951057

What OpenQuestion holds

Textmetadata
LicenceTDM
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.