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Fig. 2

ID
ZDB-IMAGE-230112-2
Source
Figures for Anderson et al., 2021
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Figure Caption

Fig. 2

Tbx5b mutants and knock-downs express early fin bud signaling molecules.

(a-c’’) Lateral views with anterior to the left. Scale bars=10 μm. (a-a’’) shha (arrows) is expressed in the posterior mesenchyme of the fin bud at 32 hours post fertilization (hpf) in wt embryos (a), tbx5b mutant (a’), and Tbx5b knock-down (a’’) embryos. (b-b’’) dlx2a (arrows) is expressed in the AER of the fin bud at 32 hpf in the wt (b), tbx5b mutant (b’) and Tbx5b knock-down (b’’) embryos, (c-c’’) bmp4 (arrows) is expressed in the wt fin at 48 hpf (c). tbx5b mutant (c’) and Tbx5b knock-down (c’’) embryos, (d-d’’’) Arrows indicate the normal location of fgf24 expression in the fin field at 21 hpf. Embryos are shown in a dorsal view with anterior to the top. Scale bar =100μm. (d) fgf24 is expressed in the fin field of wildtype embryos. (d’) fgf24 is absent from the fin field of Tbx5a knock-down embryos. (d’’) fgf24 expression is decreased in the fin field of Tbx5b knock-down embryos. (d’’’) fgf24 expression is absent in double knock-down embryos.

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Reprinted from Developmental Biology, 481, Anderson, E.B., Mao, Q., Ho, R.K., Tbx5a and Tbx5b paralogues act in combination to control separate vectors of migration in the fin field of zebrafish, 201-214, Copyright (2021) with permission from Elsevier. Full text @ Dev. Biol.