|ZFIN ID: ZDB-PUB-100625-18|
Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis
Gao, C., Wang, G., Amack, J.D., and Mitchell, D.R.
|Source:||Developmental dynamics : an official publication of the American Association of Anatomists 239(8): 2190-2197 (Journal)|
|Registered Authors:||Amack, Jeffrey, Gao, Chunlei, Wang, Guangliang (Johnny)|
|Keywords:||cilia, asymmetry, intraflagellar transport, axonemal dynein, situs inversus|
|PubMed:||20568242 Full text @ Dev. Dyn.|
Gao, C., Wang, G., Amack, J.D., and Mitchell, D.R. (2010) Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis. Developmental dynamics : an official publication of the American Association of Anatomists. 239(8):2190-2197.
ABSTRACTIn the alga Chlamydomonas reinhardtii, Oda16 functions during ciliary assembly as an adaptor for intraflagellar transport of outer arm dynein. Oda16 orthologs only occur in genomes of organisms that use motile cilia; however, such cilia play multiple roles during vertebrate development and the contribution of Oda16 to their assembly remains unexplored. We demonstrate that the zebrafish Oda16 ortholog (Wdr69) is expressed in organs with motile cilia and retains a role in dynein assembly. Antisense morpholino knockdown of Wdr69 disrupts ciliary motility and results in multiple phenotypes associated with vertebrate ciliopathies. Affected cilia included those in Kupffer's vesicle, where Wdr69 plays a role in generation of asymmetric fluid flow and establishment of organ laterality, and otic vesicles, where Wdr69 is needed to develop normal numbers of otoliths. Analysis of cilium ultrastructure revealed loss of outer dynein arms in morphant embryos. These results support a remarkable level of functional conservation for Oda16/Wdr69.