Evidence map›Paper›PMID 23872330›Full record

ArticleDevelopmental biology2013

The N-BAR domain protein, Bin3, regulates Rac1- and Cdc42-dependent processes in myogenesis.

Adriana Simionescu-Bankston, Giovanna Leoni, Yanru Wang, Peter P Pham, Arivudainambi Ramalingam, James B DuHadaway, Victor Faundez, Asma Nusrat, George C Prendergast, Grace K Pavlath

Abstract read
In one paragraph

Article in Developmental biology, 2013. 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
1.3field-weighted citation impact, top 20% 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, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. RNAi Screen inG3 (Bethesda, Md.) · 2019
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Structure-function analysis of myomaker domains required for myoblast fusion.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  15. Article
  16. Membrane fusion in muscle development and repair.Seminars in cell & developmental biology · 2015
    Review
  17. Creatine kinase B is necessary to limit myoblast fusion during myogenesis.American journal of physiology. Cell physiology · 2015
    Article
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 1 country.

Adriana Simionescu-BankstonGraduate Program in Biochemistry, Cell and Developmental Biology, Emory University School of Medicine, Atlanta, GA 30322, USA; Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Giovanna Leoni
Yanru Wang
Peter P Pham
Arivudainambi Ramalingam
James B DuHadaway
Victor Faundez
Asma Nusrat
George C Prendergast
Grace K Pavlath
Emory University · USLankenau Institute for Medical Research · USLoyola University Chicago · USTulane University · US

Funding

Regulation of intestinal epithelial barrier function by intercellular junction proteins in health and diseaseR01DK059888 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ASMA NUSRAT · 2001 to 2026
$10.5M
Molecular Physiology of Recovery from Muscle AtrophyR01AR047314 · NIAMS · EMORY UNIVERSITY · PI PAVLATH, GRACE K · 2001 to 2012
$3.0M
Cellular Mechanisms of Neuronal Metal Transport and ToxicityR01GM077569 · NIGMS · EMORY UNIVERSITY · PI FAUNDEZ, VICTOR · 2006 to 2016
$2.6M
Mechanisms of Endosome Trafficking in NeuronsR01NS042599 · NINDS · EMORY UNIVERSITY · PI FAUNDEZ, VICTOR · 2003 to 2012
$2.5M
Mechanisms of Endosome Trafficking in NeuronsR56NS042599 · NINDS · EMORY UNIVERSITY · PI FAUNDEZ, VICTOR · 2008 to 2008
$339k
NIAMS NIH HHS AR-04731408NIAMS NIH HHS R01 AR047314NIDDK NIH HHS DK59888NIDDK NIH HHS R01 DK059888NIGMS NIH HHS GM077569NIGMS NIH HHS R01 GM077569NINDS NIH HHS NS42599NINDS NIH HHS R01 NS042599NINDS NIH HHS R56 NS042599
6 · The paper itself

Abstract

Actin dynamics are necessary at multiple steps in the formation of multinucleated muscle cells. BAR domain proteins can regulate actin dynamics in several cell types, but have been little studied in skeletal muscle. Here, we identify novel functions for the N-BAR domain protein, Bridging integrator 3 (Bin3), during myogenesis in mice. Bin3 plays an important role in regulating myofiber size in vitro and in vivo. During early myogenesis, Bin3 promotes migration of differentiated muscle cells, where it colocalizes with F-actin in lamellipodia. In addition, Bin3 forms a complex with Rac1 and Cdc42, Rho GTPases involved in actin polymerization, which are known to be essential for myotube formation. Importantly, a Bin3-dependent pathway is a major regulator of Rac1 and Cdc42 activity in differentiated muscle cells. Overall, these data classify N-BAR domain proteins as novel regulators of actin-dependent processes in myogenesis, and further implicate BAR domain proteins in muscle growth and repair.

Indexed as

Muscle DevelopmentActinsAnimalscdc42 GTP-Binding ProteinCell MovementEndocytosisMiceMice, Inbred C57BLMice, KnockoutMicrofilament ProteinsMuscle Fibers, SkeletalNeuropeptidesProtein Structure, TertiaryPseudopodiarac1 GTP-Binding ProteinRegenerationActinscdc42 GTP-Binding ProteinCdc42 protein, mouseMicrofilament ProteinsNeuropeptidesrac1 GTP-Binding ProteinRac1 protein, mouseBARBAR domainBinBin-Amphiphysin-RvsBridging integratorCdc42Cross-sectional areaCSADifferentiation mediaDMdomainEmbryonic myosin heavy chaineMyHCF-actinFilamentous actinGAPGEFGMGRAF1Growth mediaGTPase-activating proteinGTPase regulator associated with focal adhesion kinase-1Guanine nucleotide exchange factorKnockoutKOMuscle regenerationMyogenesisp21-activated protein kinasePAKPBDp21-bindingRac1RetrovirusRVWild-typeWT

Identifiers

PMID23872330
PMCPMC3783639
OpenAlexW2015814220

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.