Evidence map›Paper›PMID 24821989›Full record

ArticleDevelopment (Cambridge, England)2014

PI(4,5)P2 regulates myoblast fusion through Arp2/3 regulator localization at the fusion site.

Ingo Bothe, Su Deng, Mary Baylies

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Membrane Ruffles: Composition, Function, Formation and Visualization.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Transient inhibition of lysosomal functions potentiates nucleic acid vaccines.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
  7. Cells · 2022
    Review
  8. Review
  9. Article
  10. Annual review of genetics · 2019
    Review
  11. The fusogenic synapse at a glance.Journal of cell science · 2019
    Review
  12. How cells fuse.The Journal of cell biology · 2019
    Review
  13. Article
  14. Article
  15. Review
  16. Real-time insights into regulated exocytosis.Journal of cell science · 2017
    Review
  17. Article
  18. Article
  19. Article
  20. Membrane fusion in muscle development and repair.Seminars in cell & developmental biology · 2015
    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.

Ingo BotheProgram in Developmental Biology, Sloan Kettering Institute, New York, NY 10065, USA.
Su DengGraduate Program in Physiology, Biophysics & Systems Biology, Weill Cornell Graduate School of Medical Sciences, Cornell University, New York, NY 10065, USA.
Mary BayliesProgram in Developmental Biology, Sloan Kettering Institute, New York, NY 10065, USA Graduate Program in Physiology, Biophysics & Systems Biology, Weill Cornell Graduate School of Medical Sciences, Cornell University, New York, NY 10065, USA m-baylies@ski.mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Mechanisms Regulating Myoblast Fusion in DrosophilaR01GM078318 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI BAYLIES, MARY K · 2007 to 2010
$2.0M
NCI NIH HHS P30 CA008748NIGMS NIH HHS GM078318NIGMS NIH HHS R01 GM078318
6 · The paper itself

Abstract

Cell-cell fusion is a regulated process that requires merging of the opposing membranes and underlying cytoskeletons. However, the integration between membrane and cytoskeleton signaling during fusion is not known. Using Drosophila, we demonstrate that the membrane phosphoinositide PI(4,5)P2 is a crucial regulator of F-actin dynamics during myoblast fusion. PI(4,5)P2 is locally enriched and colocalizes spatially and temporally with the F-actin focus that defines the fusion site. PI(4,5)P2 enrichment depends on receptor engagement but is upstream or parallel to actin remodeling. Regulators of actin branching via Arp2/3 colocalize with PI(4,5)P2 in vivo and bind PI(4,5)P2 in vitro. Manipulation of PI(4,5)P2 availability leads to impaired fusion, with a reduction in the F-actin focus size and altered focus morphology. Mechanistically, the changes in the actin focus are due to a failure in the enrichment of actin regulators at the fusion site. Moreover, improper localization of these regulators hinders expansion of the fusion interface. Thus, PI(4,5)P2 enrichment at the fusion site encodes spatial and temporal information that regulates fusion progression through the localization of activators of actin polymerization.

Indexed as

Gene Expression Regulation, DevelopmentalActin-Related Protein 2-3 ComplexActinsAnimalsCell CommunicationCell MembraneCytoskeletonDrosophila melanogasterGenotypeMuscle Fibers, SkeletalMutationMyoblastsPhosphatidylinositol 4,5-DiphosphatePhospholipidsrac GTP-Binding ProteinsSignal TransductionActin-Related Protein 2-3 ComplexActinsPhosphatidylinositol 4,5-DiphosphatePhospholipidsrac GTP-Binding ProteinsActin regulationArp2/3 regulatorsDrosophilaMyoblast fusionPI(4,5)P2PtdIns(4,5)P2

Identifiers

PMID24821989
PMCPMC4034421

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.