Research Article
Craniofacial skeletal defects of adult zebrafish Glypican 4 (knypek) mutants
Article first published online: 23 SEP 2009
DOI: 10.1002/dvdy.22086
Copyright © 2009 Wiley-Liss, Inc.
Additional Information
How to Cite
LeClair, E. E., Mui, S. R., Huang, A., Topczewska, J. M. and Topczewski, J. (2009), Craniofacial skeletal defects of adult zebrafish Glypican 4 (knypek) mutants. Dev. Dyn., 238: 2550–2563. doi: 10.1002/dvdy.22086
Publication History
- Issue published online: 23 SEP 2009
- Article first published online: 23 SEP 2009
- Manuscript Accepted: 29 JUL 2009
Funded by
- NIH/NIDCR. Grant Number: DE016678
- DePaul University Research Council
Keywords:
- zebrafish;
- glypican;
- knypek;
- craniofacial;
- skull;
- jaw;
- bone;
- cartilage;
- morphometrics
Abstract
The heparan sulfate proteoglycan Glypican 4 (Gpc4) is part of the Wnt/planar cell polarity pathway, which is required for convergence and extension during zebrafish gastrulation. To observe Glypican 4-deficient phenotypes at later stages, we rescued gpc4−/− (knypek) homozygotes and raised them for more than one year. Adult mutants showed diverse cranial malformations of both dermal and endochondral bones, ranging from shortening of the rostral-most skull to loss of the symplectic. Additionally, the adult palatoquadrate cartilage was disorganized, with abnormal chondrocyte orientation. To understand how the palatoquadrate cartilage normally develops, we examined a juvenile series of wild type and mutant specimens. This identified two novel domains of elongated chondrocytes in the larval palatoquadrate, which normally form prior to endochondral ossification. In contrast, gpc4−/− larvae never form these domains, suggesting a failure of chondrocyte orientation, though not differentiation. Our findings implicate Gpc4 in the regulation of zebrafish cartilage and bone morphogenesis. Developmental Dynamics 238:2550–2563, 2009. © 2009 Wiley-Liss, Inc.

1097-0177/asset/DVDY_left.gif?v=1&s=b87335326ab8ecd1f573539da0b5fa6abef26532)
