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Surface apposition and multiple cell contacts promote myoblast fusion in Drosophila flight muscles

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TLDR
Transmission EM methods reveal that cell–cell fusion of individual myoblasts with growing Drosophila flight muscles is a stepwise process in which the cell adhesion and branched actin machineries mediate tight apposition and formation of multiple contacts and pores between the surfaces of the fusing cells.
Abstract
Fusion of individual myoblasts to form multinucleated myofibers constitutes a widely conserved program for growth of the somatic musculature. We have used electron microscopy methods to study this key form of cell–cell fusion during development of the indirect flight muscles (IFMs) of Drosophila melanogaster. We find that IFM myoblast–myotube fusion proceeds in a stepwise fashion and is governed by apparent cross talk between transmembrane and cytoskeletal elements. Our analysis suggests that cell adhesion is necessary for bringing myoblasts to within a minimal distance from the myotubes. The branched actin polymerization machinery acts subsequently to promote tight apposition between the surfaces of the two cell types and formation of multiple sites of cell–cell contact, giving rise to nascent fusion pores whose expansion establishes full cytoplasmic continuity. Given the conserved features of IFM myogenesis, this sequence of cell interactions and membrane events and the mechanistic significance of cell adhesion elements and the actin-based cytoskeleton are likely to represent general principles of the myoblast fusion process.

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Journal ArticleDOI

The hallmarks of cell-cell fusion.

TL;DR: How fusogens surmount multiple energy barriers to mediate cell-cell fusion is reviewed, including how early preparatory steps bring membranes to a distance of ∼10 nm, while fusogen act in the final approach between membranes.
Journal ArticleDOI

How cells fuse.

TL;DR: Brukman et al. review cell–cell fusion mechanisms, focusing on the identity of the fusogens that mediate these processes and the regulation of their activities.
Journal ArticleDOI

Myoblast fusion confusion: the resolution begins.

TL;DR: The latest findings regarding the biology of Myomaker and Minion–Myomerger are reviewed, places these findings in the context of known pathways in mammalian myoblast fusion, and highlights areas that require further investigation.
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Cell Fusion: Merging Membranes and Making Muscle

TL;DR: This work highlights the discovery and activities of several key sets of fusion proteins that together offer an evolving perspective on cell membrane fusion in vertebrates and skeletal muscle.
Journal ArticleDOI

Structure–function analysis of myomaker domains required for myoblast fusion

TL;DR: The data indicate that the majority of myomaker is embedded in the plasma membrane with seven membrane-spanning regions and a required intracellular C-terminal tail, and this findings represent an important step toward deciphering the cellular components and mechanisms that control myoblast fusion and muscle formation.
References
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Journal ArticleDOI

Fiji: an open-source platform for biological-image analysis

TL;DR: Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis that facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system.
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Computer Visualization of Three-Dimensional Image Data Using IMOD

TL;DR: IMOD is useful for studying and modeling data from tomographic, serial section, and optical section reconstructions and allows image data to be visualized by several different methods.
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Automated electron microscope tomography using robust prediction of specimen movements.

TL;DR: A new method was developed to acquire images automatically at a series of specimen tilts, as required for tomographic reconstruction, using changes in specimen position at previous tilt angles to predict the position at the current tilt angle.
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A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila

TL;DR: The generation and validation of a genome-wide library of Drosophila melanogaster RNAi transgenes, enabling the conditional inactivation of gene function in specific tissues of the intact organism and opening up the prospect of systematically analysing gene functions in any tissue and at any stage of the Drosophile lifespan.
Journal ArticleDOI

Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis.

Tzumin Lee, +1 more
- 01 Mar 1999 - 
TL;DR: A genetic mosaic system in Drosophila is described, in which a dominant repressor of a cell marker is placed in trans to a mutant gene of interest, which allows for the study of gene functions in neuroblast proliferation, axon guidance, and dendritic elaboration in the complex central nervous system.
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