dact1/2modifies noncanonical Wnt signaling andcalpain 8expression to regulate convergent extension and craniofacial development

Author:

Carroll Shannon H.,Schafer Sogand,Kawasaki Kenta,Tsimbal Casey,Julé Amélie M.,Hallett Shawn A.ORCID,Li Edward,Liao Eric C.

Abstract

AbstractWnt signaling plays a crucial role in the early embryonic patterning and development, to regulate convergent extension during gastrulation and the establishment of the dorsal axis. Further, Wnt signaling is a crucial regulator of craniofacial morphogenesis. The adapter proteins Dact1 and Dact2 modulate the Wnt signaling pathway through binding to Disheveled, however, the distinct relative functions of Dact1 and Dact2 during embryogenesis remain unclear. We found thatdact1anddact2genes have dynamic spatiotemporal expression domains that are reciprocal to one another and townt11f2l, that suggest distinct functions during zebrafish embryogenesis. We found that bothdact1anddact2contribute to axis extension, with compound mutants exhibiting a similar convergent extension defect and craniofacial phenotype to thewnt11f2mutant. Utilizing single-cell RNAseq andgpc4mutant that disrupts noncanonical Wnt signaling, we identifieddact1/2specific roles during early development. Comparative whole transcriptome analysis between wildtype,gpc4anddact1/2mutants revealed a novel role fordact1/2in regulating the mRNA expression of the classical calpaincapn8. Over-expression ofcapn8phenocopiesdact1/2craniofacial dysmorphology. These results identify a previously unappreciated role ofcapn8and calcium-dependent proteolysis during embryogenesis. Taken together, our findings highlight the distinct and overlapping roles ofdact1anddact2in embryonic craniofacial development, providing new insights into the multifaceted regulation of Wnt signaling.

Publisher

Cold Spring Harbor Laboratory

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