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wnt16 regulates spine and muscle morphogenesis through parallel signals from notochord and dermomyotome.

Claire J WatsonW Joyce TangMaria F RojasImke A K FiedlerErnesto Morfin Montes de OcaAndrea R CronrathLulu K CalliesAvery Angell SwearerAli R AhmedVisali SethuramanSumaya AddishGist H FarrArianna Ericka GomezJyoti RaiAdrian T Monstad-RiosEdith M GardinerDavid KarasikLisa MavesBjorn BusseYi-Hsiang HsuRonald Young Kwon
Published in: PLoS genetics (2022)
Bone and muscle are coupled through developmental, mechanical, paracrine, and autocrine signals. Genetic variants at the CPED1-WNT16 locus are dually associated with bone- and muscle-related traits. While Wnt16 is necessary for bone mass and strength, this fails to explain pleiotropy at this locus. Here, we show wnt16 is required for spine and muscle morphogenesis in zebrafish. In embryos, wnt16 is expressed in dermomyotome and developing notochord, and contributes to larval myotome morphology and notochord elongation. Later, wnt16 is expressed at the ventral midline of the notochord sheath, and contributes to spine mineralization and osteoblast recruitment. Morphological changes in wnt16 mutant larvae are mirrored in adults, indicating that wnt16 impacts bone and muscle morphology throughout the lifespan. Finally, we show that wnt16 is a gene of major effect on lean mass at the CPED1-WNT16 locus. Our findings indicate that Wnt16 is secreted in structures adjacent to developing bone (notochord) and muscle (dermomyotome) where it affects the morphogenesis of each tissue, thereby rendering wnt16 expression into dual effects on bone and muscle morphology. This work expands our understanding of wnt16 in musculoskeletal development and supports the potential for variants to act through WNT16 to influence bone and muscle via parallel morphogenetic processes.
Keyphrases
  • cell proliferation
  • stem cells
  • bone mineral density
  • skeletal muscle
  • poor prognosis
  • bone regeneration
  • spinal cord
  • body composition
  • bone loss
  • deep brain stimulation