Fig. 7
sox2can substitute forsox3during early otic development. (A-D) Dorsal views (anterior to the top) showing expression of pax2a at 12 hpf in a control embryo (A), a sox3-morphant (B), a hs:sox2/+ heterozygote (C) and hs:sox2/+ heterozygote injected with sox3-mo (D). Embryonic staging was confirmed with myoD expression in somites. Embryos were heat shocked at 35 °C from 10 to 12 hpf. sox3-morphants in (B) and (D) were injected with 5 ng each of sox3-mo. (E) Box-and-whisker plots of relative surface area of the otic/epibranchial domain of pax2a at 12 hpf in controls, sox3-morphants, hs:sox2/+ heterozygotes and hs:sox2/+ heterozygotes injected with sox3-mo. Data are normalized relative to control groups, with means indicated by green lines. Asterisks indicate statistically significant differences compare to control (** P<0.01, Tukey's HSD test). n.s., no significant difference compared to controls. |
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Stage: | 5-9 somites |
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Stage: | 5-9 somites |
Reprinted from Developmental Biology, 435(1), Gou, Y., Guo, J., Maulding, K., Riley, B.B., sox2 and sox3 cooperate to regulate otic/epibranchial placode induction in zebrafish, 84-95, Copyright (2018) with permission from Elsevier. Full text @ Dev. Biol.