Literature DB >> 17419995

A critical function for the actin cytoskeleton in targeted exocytosis of prefusion vesicles during myoblast fusion.

Sangjoon Kim1, Khurts Shilagardi, Shiliang Zhang, Sabrina N Hong, Kristin L Sens, Jinyan Bo, Guillermo A Gonzalez, Elizabeth H Chen.   

Abstract

Myoblast fusion is an essential step during muscle differentiation. Previous studies in Drosophila have revealed a signaling pathway that relays the fusion signal from the plasma membrane to the actin cytoskeleton. However, the function for the actin cytoskeleton in myoblast fusion remains unclear. Here we describe the characterization of solitary (sltr), a component of the myoblast fusion signaling cascade. sltr encodes the Drosophila ortholog of the mammalian WASP-interacting protein. Sltr is recruited to sites of fusion by the fusion-competent cell-specific receptor Sns and acts as a positive regulator for actin polymerization at these sites. Electron microscopy analysis suggests that formation of F-actin-enriched foci at sites of fusion is involved in the proper targeting and coating of prefusion vesicles. These studies reveal a surprising cell-type specificity of Sltr-mediated actin polymerization in myoblast fusion, and demonstrate that targeted exocytosis of prefusion vesicles is a critical step prior to plasma membrane fusion.

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Year:  2007        PMID: 17419995     DOI: 10.1016/j.devcel.2007.02.019

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  93 in total

1.  The actin cytoskeleton inhibits pore expansion during PIV5 fusion protein-promoted cell-cell fusion.

Authors:  Mark A Wurth; Rachel M Schowalter; Everett Clinton Smith; Carole L Moncman; Rebecca Ellis Dutch; Richard O McCann
Journal:  Virology       Date:  2010-08-15       Impact factor: 3.616

2.  Rapid fusion and syncytium formation of heterologous cells upon expression of the FGFRL1 receptor.

Authors:  Florian Steinberg; Simon D Gerber; Thorsten Rieckmann; Beat Trueb
Journal:  J Biol Chem       Date:  2010-09-17       Impact factor: 5.157

Review 3.  Myoblast fusion: lessons from flies and mice.

Authors:  Susan M Abmayr; Grace K Pavlath
Journal:  Development       Date:  2012-02       Impact factor: 6.868

4.  3D analysis of founder cell and fusion competent myoblast arrangements outlines a new model of myoblast fusion.

Authors:  Karen Beckett; Mary K Baylies
Journal:  Dev Biol       Date:  2007-07-06       Impact factor: 3.582

Review 5.  Visualizing new dimensions in Drosophila myoblast fusion.

Authors:  Brian Richardson; Karen Beckett; Mary Baylies
Journal:  Bioessays       Date:  2008-05       Impact factor: 4.345

6.  Ultrastructural analysis of myoblast fusion in Drosophila.

Authors:  Shiliang Zhang; Elizabeth H Chen
Journal:  Methods Mol Biol       Date:  2008

7.  Insights into the localization and function of myomaker during myoblast fusion.

Authors:  Dilani G Gamage; Eugenia Leikina; Malgorzata E Quinn; Anthony Ratinov; Leonid V Chernomordik; Douglas P Millay
Journal:  J Biol Chem       Date:  2017-08-31       Impact factor: 5.157

8.  RacGAP50C directs perinuclear gamma-tubulin localization to organize the uniform microtubule array required for Drosophila myotube extension.

Authors:  Colleen M Guerin; Sunita G Kramer
Journal:  Development       Date:  2009-03-18       Impact factor: 6.868

9.  Cytoskeletal remodeling during myotube assembly and guidance: coordinating the actin and microtubule networks.

Authors:  Colleen M Guerin; Sunita G Kramer
Journal:  Commun Integr Biol       Date:  2009-09

10.  The small G-proteins Rac1 and Cdc42 are essential for myoblast fusion in the mouse.

Authors:  Elena Vasyutina; Benedetta Martarelli; Cord Brakebusch; Hagen Wende; Carmen Birchmeier
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-14       Impact factor: 11.205

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