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Fig. s2 Cartilage and bone markers, sox9a and runx2a, are reduced in the pharyngeal arches with loss of prdm3 in zebrafish. (A-B) Wildtype or prdm3−/− mutant embryos were collected and in situ hybridization was performed for sox9a (A) or runx2a (B) at 48 hpf. Shown are ventral views for each transcript. Black arrow heads indicate areas of decreased expression of these markers in the developing viscerocranium and neurocranium. Scale bars, 250 μm. Abbreviations: eye (e).
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Reprinted from Developmental Biology, 461(2), Shull, L.C., Sen, R., Menzel, J., Goyama, S., Kurokawa, M., Artinger, K.B., The conserved and divergent roles of Prdm3 and Prdm16 in zebrafish and mouse craniofacial development, 132-144, Copyright (2020) with permission from Elsevier. Full text @ Dev. Biol.