Spatiotemporal control of myoblast identity drives muscle diversity in the <i>Drosophila</i> leg

Пространственно-временной контроль идентичности миобластов определяет разнообразие мышц в ноге Drosophila
Sandrine Hughes, Yad Ghavi-Helm, Isabelle Stévant, Guillaume Marcy, Benjamin Gillet, Camille Guillermin, Violaine Tribollet, Mathilde Bouchet, Anne Laurençon, Dan Zhou, Sergio Sarnataro, Laurent Gilquin, Emeric Texeraud, Samantha VONAU, Jonathan Enriquez
2026-07-01

Dpp/BMPDrosophila leg musclesWg/Wnt1myoblast fusion transcriptional identitymyoblast spatiotemporal specification
leg muscles, we show that naïve mesodermal precursors undergo stepwise specification orchestrated by epithelial morphogens. Wg/Wnt1 and Dpp/BMP first restrict multipotent precursors into proximal and distal lineages. Within the distal lineage, successive fate bifurcations generate distinct muscle subtypes and a separate nonmuscle lineage of neuronal lamella cells. Focusing on one lineage, we demonstrate that Wg and Dpp act again to control the spatiotemporal deployment of transcription factors, ensuring that groups of myoblasts destined to fuse to produce a specific muscle share a coordinated transcriptional identity. Thus, epithelial morphogens not only pattern the epithelium but also synchronize myoblast specification, enabling the emergence of diverse muscles from syncytial fibers. Our findings provide a framework for the developmental and evolutionary origins of appendicular muscles and may help explain the selective vulnerability of specific muscles in muscular dystrophies.
1
Epithelial morphogens both pattern the epithelium and coordinate myoblast specification, enabling diverse muscles to arise from syncytial fibers.
2
This spatiotemporal control framework helps explain developmental and evolutionary origins of appendicular muscles and may underlie selective muscle vulnerability in muscular dystrophies.
3
Wg and Dpp later control spatiotemporal deployment of transcription factors to synchronize myoblast groups that will fuse into specific muscles.
4
Wg/Wnt1 and Dpp/BMP morphogens partition naïve mesodermal precursors into proximal and distal leg muscle lineages.
5
Within the distal lineage, successive fate bifurcations generate distinct muscle subtypes and a separate nonmuscle neuronal lamella cell lineage.

Myoblast populations (mesodermal precursors and specified myoblasts) driving leg muscle formation in Drosophila

Spatiotemporal control of myoblast identity by epithelial morphogens (Wg/Wnt1 and Dpp/BMP) that patterns lineage bifurcations, coordinates transcriptional programs for myoblast fusion, and generates muscle diversity in the Drosophila leg

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2026-07-01
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Sandrine Hughes
Yad Ghavi-Helm
Isabelle Stévant
Guillaume Marcy
Benjamin Gillet
Camille Guillermin
Violaine Tribollet
Mathilde Bouchet
Anne Laurençon
Dan Zhou
Sergio Sarnataro
Laurent Gilquin
Emeric Texeraud
Samantha VONAU
Jonathan Enriquez
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