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Published September 14, 2015 | Accepted Version + Supplemental Material
Journal Article Open

Axud1 Integrates Wnt Signaling and Transcriptional Inputs to Drive Neural Crest Formation

Abstract

Neural crest cells are induced at the neural plate border by the combined action of transcription factors and signaling molecules. Here, we show that Axud1, a downstream effector of Wnt signaling, represents a critical missing link that integrates signaling and transcriptional cues to mediate neural crest formation. Axud1 is a transcription factor expressed in neural crest progenitors in a Wnt1/β-catenin-dependent manner. Axud1 loss leads to downregulation of multiple genes involved in neural crest specification, similar to the effects of Wnt1 knockdown. Importantly, Axud1 is sufficient to rescue neural crest formation after disruption of Wnt signaling. Furthermore, it physically interacts with neural plate border genes Pax7 and Msx1 in vivo to directly activate transcription of stem cell factor FoxD3, initiating the neural crest program. Thus, Axud1 integrates Wnt signaling with transcriptional inputs to endow the neural crest with its unique molecular signature.

Additional Information

© 2015 Elsevier. Received: February 23, 2015; Revised: May 26, 2015; Accepted: June 29, 2015; Published: August 6, 2015. We thank Joanne Tan-Cabugao, Brian Jun, and Daniel S.E. Koo for technical assistance. This work was supported by NIH grants DE024157 and HD037105 to M.E.B. M.S.-C. was funded by a fellowship from the Pew Fellows Program in Biomedical Sciences and by NIH grant K99DE024232. M.S. was funded by a Caltech SURF fellowship. AUTHOR CONTRIBUTIONS: M.S.-C. and M.E.B. conceived and designed the experimental approach. M.S.-C. and M.S. performed the experiments and analyzed the data. M.S.-C. and M.E.B. wrote the manuscript.

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Accepted Version - nihms-709420.pdf

Supplemental Material - mmc1.pdf

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