AI Article Synopsis

  • The segmentation of the axial skeleton in amniotes relies on a mechanism called the segmentation clock, which organizes the paraxial mesoderm and sclerotome.
  • In zebrafish, although the paraxial segmentation is significantly disrupted, the segmentation of the chordacentra remains mostly normal, indicating a complex relationship.
  • The study reveals that the cells in the notochord sheath are crucial for mineralizing the chordacentrum and adapting to myotome patterns, suggesting an independent yet responsive segmentation process, distinct from the segmentation clock seen in other species.

Article Abstract

Segmentation of the axial skeleton in amniotes depends on the segmentation clock, which patterns the paraxial mesoderm and the sclerotome. While the segmentation clock clearly operates in teleosts, the role of the sclerotome in establishing the axial skeleton is unclear. We severely disrupt zebrafish paraxial segmentation, yet observe a largely normal segmentation process of the chordacentra. We demonstrate that axial notochord sheath cells are responsible for chordacentrum mineralization, and serve as a marker for axial segmentation. While autonomous within the notochord sheath, expression and centrum formation show some plasticity and can respond to myotome pattern. These observations reveal for the first time the dynamics of notochord segmentation in a teleost, and are consistent with an autonomous patterning mechanism that is influenced, but not determined by adjacent paraxial mesoderm. This behavior is not consistent with a clock-type mechanism in the notochord.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5962341PMC
http://dx.doi.org/10.7554/eLife.33843DOI Listing

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