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Updated: Feb 6, 2026

Assessing Primary Neurogenesis in Xenopus Embryos Using Immunostaining
Published on: April 12, 2016
Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos
Helen Rankin Willsey1, Peter Walentek2, Cameron R T Exner3
1Department of Molecular&Cell Biology, University of California, Berkeley, USA; Department of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, USA.
Abstract:
Microtubule remodeling is critical for cellular and developmental processes underlying morphogenetic changes and for the formation of many subcellular structures. Katanins are conserved microtubule severing enzymes that are essential for spindle assembly, ciliogenesis, cell division, and cellular motility. We have recently shown that a related protein, Katanin-like 2 (KATNAL2), is similarly required for cytokinesis, cell cycle progression, and ciliogenesis in cultured mouse cells. However, its developmental expression pattern, localization, and in vivo role during organogenesis have yet to be characterized. Here, we used Xenopus embryos to reveal that Katnal2 (1) is expressed broadly in ciliated and neurogenic tissues throughout embryonic development; (2) is localized to basal bodies, ciliary axonemes, centrioles, and mitotic spindles; and (3) is required for ciliogenesis and brain development. Since human KATNAL2 is a risk gene for autism spectrum disorders, our functional data suggest that Xenopus may be a relevant system for understanding the relationship of mutations in this gene to autism and the underlying molecular mechanisms of pathogenesis.
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