Sox11 genes affect neuronal differentiation in the developing zebrafish enteric nervous system

• 成果类型: Article
• 署名作者: Huang, Yuanyun; Li, Can; Rajan, Ayyappa Raja Desingu; Bronner, Marianne E.
• 署名单位: California Institute of Technology
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-10983
• DOI: 10.1073/pnas.2510548122
• 发表日期: 2025-08-11
• 关键词: hirschsprungs-disease; expression patterns; suggests; phox2b; specification; mutations; migration; genetics; roles; hand2

摘要

The vertebrate enteric nervous system (ENS) is derived from vagal neural crest cells, which enter the foregut as progenitors that migrate from rostral to caudal to populate the entire length of the gut. Here, we show that transcription factors sox11a and sox11b, zebrafish orthologs of the human SOX11 gene, are highly expressed in neural crest cells transitioning from progenitors to differentiating neuronal subtypes. Accordingly, CRISPR-Cas9 depletion shows that loss of sox11 paralogs reduces the number of neurons that express the inhibitory motor neuron marker adcyap1b without affecting cell proliferation or death. Transcription factor footprinting analysis of open chromatin regions identified by ATAC-seq reveals Sox11 binding sites in the adcyap1b enhancer. Furthermore, mutational analysis shows these binding sites are required for mediating enhancer-driven reporter expression. Taken together, our results demonstrate an important and previously unrecognized role for sox11a and sox11b in neuronal subtype specification in the developing zebrafish ENS.