XB-IMG-154589
Xenbase Image ID: 154589
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Figure 6
hairy genes participate in the early formation of neural crest cells. A–X: Dorsal views of Xenopus laevis embryos; anterior side is on the right. The injected side is indicated by an arrowhead. Embryos were injected into one blastomere at the 8- to 16-cell stage with 700 ng of mRNA, treated with dexamethasone stage 11 until neurula stages and fixed, and the expression of several markers was analyzed by in situ hybridization. No change was observed in the control injected embryos nonincubated with dexamethasone (insets in A, E, I, M, Q, and U). A–L: Gain of function. hairy activator constructs mRNA-injected embryos show increased expression of snail2 (A,E,I) while neural plate marker sox2 (B,F,J) and epidermis marker xk81a (C,G,K) are reduced. D,H,L: Embryos labeled by double in situ hybridization for sox2 and xk81a genes showing the increase in prospective neural crest region (black brackets) in the injected side (arrowheads). M–X: Loss of function. Conversely, DNhairy constructs mRNA-injected embryos show that neural crest markers snail2 are reduced in the injected side (M,Q,U) while neural plate marker sox2 (N,R,V) and the epidermis marker xk81a (O,S,W) are slightly increased. P′, T′, X′: Rescue of DNhairy by coinjecting mRNA of hairy activator constructs. The phenotype of the neural crest marker foxd3 was rescued by the co-injection of hairy1-GR (P′), hairy2a-GR (T′) and hairy2b-GR (X′). P,T,X: Embryos labeled by double in situ hybridization for sox2 and xk81a genes showing the decrease in prospective neural crest territory (black brackets indicate width) in the injected side. Image published in: Vega-López GA et al. (2015) Copyright © 2015. Image reproduced with permission of the Publisher, John Wiley & Sons.
Image source: Published
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