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Hox - Meis-relayed topographical genetic switch underlies cardiopharyngeal neural crest diversification, revealed by multimodal analysis

Iwase, A.; Uchijima, Y.; Seya, D.; Kida, M.; Higashiyama, H.; Matsui, K.; Taguchi, A.; Harada, Y.; Yunce, W.; Yamamoto, S.; Fukuda, S.; Nomura, S.; Kohro, T.; Shukunami, C.; Akiyama, H.; Seki, M.; Kanai, A.; Suzuki, Y.; Kawamura, T.; Nakagawa, O.; Katoh, H.; Ishikawa, S.; Wada, Y.; Aburatani, H.; Kurihara, Y.; Miyagawa-Tomita, S.; Kurihara, H.

2025-11-11 developmental biology
10.1101/2025.11.09.687497 bioRxiv
Show abstract

Neural crest cells (NCCs) are multipotent migratory cells essential for cardiac development, yet the lineage trajectories and gene regulatory networks (GRNs) underlying their intracardiac differentiation remain unclear. Here, we integrate single-cell RNA-seq, spatial transcriptomics, and multiomic analyses to construct a comprehensive map of NCC lineages in developing mouse cardiopharyngeal tissues. We identify a transition from Hox-positive pharyngeal NCCs to Hox-negative intracardiac populations associated with the outflow tract cushion, accompanied by a shift in Meis transcription factor binding and GRN architecture. By contrast, NCCs forming the aorticopulmonary septum and great vessel smooth muscle retain distinct Hox-codes. A Meis2-Sox9-Scx GRN defines a skeletogenic progenitor-like intermediate state that gives rise to coronary artery smooth muscle and semilunar valves. Our findings suggest that the loss of Hox-dependent regional identity enables pharyngeal NCCs to acquire new fates upon entering the cardiac cushion, providing insight into the developmental origins of coronary and valvular calcification.

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