Evidence map›Paper›PMID 21925492›Full record

ArticleDevelopmental biology2011

Moleskin is essential for the formation of the myotendinous junction in Drosophila.

Ze Cindy Liu, Erika R Geisbrecht

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Developmental origin of tendon diversity inFrontiers in physiology · 2023
    Review
  2. Article
  3. Review
  4. Article
  5. Importin-7 mediates memory consolidation through regulation of nuclear translocation of training-activated MAPK in Drosophila.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  6. Article
  7. Article
  8. The development of the myotendinous junction. A review.Muscles, ligaments and tendons journal · 2012
    Article
  9. Article
  10. Morphogenesis of the somatic musculature in Drosophila melanogaster.Wiley interdisciplinary reviews. Developmental biology
    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

2 authors at 1 institution in 1 country.

Ze Cindy LiuDivision of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri, Kansas City, MO 64110, USA.
Erika R Geisbrecht
University of Missouri–Kansas City · US

Funding

IDENTIFICATION OF GENES ASSOCIATED WITH MYOBLAST FUSIONR01AR044274 · NIAMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI ABMAYR, SUSAN M · 1996 to 2012
$3.6M
The Role of Protein Turnover in a Drosophila Model of Muscle Atrophy.R03AR059311 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI GEISBRECHT, ERIKA RAE · 2010 to 2012
$219k
Identification of Genes Required for Myoblast FusionF32AR053027 · NIAMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI GEISBRECHT, ERIKA RAE · 2005 to 2007
$128k
NIAMS NIH HHS AR044274NIAMS NIH HHS AR059311.NIAMS NIH HHS F32 AR053027NIAMS NIH HHS R01 AR044274NIAMS NIH HHS R03 AR059311
6 · The paper itself

Abstract

It is the precise connectivity between skeletal muscles and their corresponding tendon cells to form a functional myotendinous junction (MTJ) that allows for the force generation required for muscle contraction and organismal movement. The Drosophila MTJ is composed of secreted extracellular matrix (ECM) proteins deposited between integrin-mediated hemi-adherens junctions on the surface of muscle and tendon cells. In this paper, we have identified a novel, cytoplasmic role for the canonical nuclear import protein Moleskin (Msk) in Drosophila embryonic somatic muscle attachment. Msk protein is enriched at muscle attachment sites in late embryogenesis and msk mutant embryos exhibit a failure in muscle-tendon cell attachment. Although the muscle-tendon attachment sites are reduced in size, components of the integrin complexes and ECM proteins are properly localized in msk mutant embryos. However, msk mutants fail to localize phosphorylated focal adhesion kinase (pFAK) to the sites of muscle-tendon cell junctions. In addition, the tendon cell specific proteins Stripe (Sr) and activated mitogen-activated protein kinase (MAPK) are reduced in msk mutant embryos. Our rescue experiments demonstrate that Msk is required in the muscle cell, but not in the tendon cells. Moreover, muscle attachment defects due to loss of Msk are rescued by an activated form of MAPK or the secreted epidermal growth factor receptor (Egfr) ligand Vein. Taken together, these findings provide strong evidence that Msk signals non-autonomously through the Vein-Egfr signaling pathway for late tendon cell late differentiation and/or maintenance.

Indexed as

AnimalsAnimals, Genetically ModifiedDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianErbB ReceptorsExtracellular Matrix ProteinsFocal Adhesion Protein-Tyrosine KinasesImmunohistochemistryIn Situ HybridizationIntegrinsKaryopherinsLuminescent ProteinsMitogen-Activated Protein KinasesMuscle, SkeletalDNA-Binding ProteinsDrosophila ProteinsEgfr protein, DrosophilaErbB ReceptorsExtracellular Matrix ProteinsFocal Adhesion Protein-Tyrosine KinasesIntegrinsKaryopherinsLuminescent ProteinsMitogen-Activated Protein KinasesMsk protein, DrosophilaNeuregulinsReceptors, Invertebrate Peptidesr protein, DrosophilaTranscription Factorsvn protein, Drosophila

Identifiers

PMID21925492
PMCPMC4066395
OpenAlexW1995301140

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.