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
2026-07-01
SCID: 54.1/tjcgqcnv
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Dpp/BMPDrosophila leg musclesWg/Wnt1myoblast fusion transcriptional identitymyoblast spatiotemporal specification
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Abstract (AI)
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.
Key Findings
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.
Research Object
Myoblast populations (mesodermal precursors and specified myoblasts) driving leg muscle formation in Drosophila
Research Subject
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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