Abstract

Znf703 is an RAR- and Wnt-inducible transcription factor that exhibits a complex expression pattern in the developing embryo: Znf703 mRNA is found in the early circumblastoporal ring, then later throughout the neural plate and its border, and subsequently in the mid/hindbrain and somites. We show that Znf703 has a different and separable function in early mesoderm versus neural crest and placode development. Independent of its early knockdown phenotype on Gdf3 and Wnt8, Znf703 disrupts patterning of distinct neural crest migratory streams normally delineated by Sox10, Twist, and Foxd3 and inhibits otocyst formation and otic expression of Sox10 and Eya1. Furthermore, Znf703 promotes massive overgrowth of SOX2+ cells, disrupting the SoxB1 balance at the neural plate border. Despite prominent expression in other neural plate border-derived cranial and sensory domains, Znf703 is selectively absent from the otocyst, suggesting that Znf703 must be specifically cleared or down-regulated for proper otic development. We show that mutation of the putative Groucho-repression domain does not ameliorate Znf703 effects on mesoderm, neural crest, and placodes. We instead provide evidence that Znf703 requires the Buttonhead domain for transcriptional repression.

Highlights

  • Znf[703] is an RAR- and Wnt-inducible transcription factor that exhibits a complex expression pattern in the developing embryo: Znf[703] mRNA is found in the early circumblastoporal ring, later throughout the neural plate and its border, and subsequently in the mid/hindbrain and somites

  • We recently identified Znf[703] as a target of RARγ7, prompting further investigation into the role of Znf[703] in early developmental processes that are sensitive to retinoic acid, such as neural crest and placodal patterning

  • Towards Znf[703] function, we investigated the highly conserved FKPY domain of Znf[703] and found that mutation of FKPY had minimal effect on transcriptional repression and developmental phenotypes compared to wild type, but that the buttonhead domain was indispensable for repression by Znf[703]

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Summary

Introduction

Znf[703] is an RAR- and Wnt-inducible transcription factor that exhibits a complex expression pattern in the developing embryo: Znf[703] mRNA is found in the early circumblastoporal ring, later throughout the neural plate and its border, and subsequently in the mid/hindbrain and somites. We recently identified Znf[703] as a target of RARγ7, prompting further investigation into the role of Znf[703] in early developmental processes that are sensitive to retinoic acid, such as neural crest and placodal patterning. Because it is expressed at the neural plate border, Znf[703] protein is positioned to interact with a variety of signaling pathways. We found that mis/overexpression of Znf[703] causes a massive expansion of SOX2+ cells, while inhibiting expression of the placode marker, Eya[1] as well as otic Sox[10] expression This results in the shrinkage or disappearance of the hollow ball of ectoderm that delineates an otocyst. Despite early phenotypes that could potentially affect neural crest competence, Znf[703] is still able to influence neural crest and placode patterning when overexpressed after gastrulation

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