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- Title
Microtubule polarity determines the lineage of embryonic neural precursor in zebrafish spinal cord.
- Authors
Richard, Clément-Alexis; Seum, Carole; Gonzalez-Gaitan, Marcos
- Abstract
The phenomenal diversity of neuronal types in the central nervous system is achieved in part by the asymmetric division of neural precursors. In zebrafish neural precursors, asymmetric dispatch of Sara endosomes (with its Notch signaling cargo) functions as fate determinant which mediates asymmetric division. Here, we found two distinct pools of neural precursors based on Sara endosome inheritance and spindle-microtubule enrichment. Symmetric or asymmetric levels of spindle-microtubules drive differently Sara endosomes inheritance and predict neural precursor lineage. We uncover that CAMSAP2a/CAMSAP3a and KIF16Ba govern microtubule asymmetry and endosome motility, unveiling the heterogeneity of neural precursors. Using a plethora of physical and cell biological assays, we determined the physical parameters and molecular mechanisms behind microtubule asymmetries and biased endosome motility. Evolutionarily, the values of those parameters explain why all sensory organ precursor cells are asymmetric in flies while, in zebrafish spinal cord, two populations of neural precursors (symmetric vs asymmetric) are possible. In Zebrafish embryos spinal cords, neural precursors are clustered in two distinct populations based on their spindle-microtubule enrichment. KIF16Ba, CAMSAP2a/3a and spindle-microtubule enrichment control Sara endosome motility and mediate neural precursor fates.
- Subjects
SPINAL cord; MICROTUBULES; BRACHYDANIO; CENTRAL nervous system; BIOLOGICAL assay; ENDOSOMES
- Publication
Communications Biology, 2024, Vol 7, Issue 1, p1
- ISSN
2399-3642
- Publication type
Article
- DOI
10.1038/s42003-024-06018-7