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Fig. 3. Head defects induced by McerP-BMP4, Xnr1 and Xwnt8 microinjection in the frog embryo. Embryos were injected at the four-to-eight-cell stage in the two dorsal-vegetal blastomeres. (A-C) Injection of 80 pg of CMV.BMP4 (A; 100%, n=22), CMV.Xnr1(B; 94%, n=17) and CMV.Xwnt8 (C; 20%, n=25) led to very severe phenotypes. (D-F) Injection of 20 pg (F; 60%, n=20), 40 pg (E; 62%, n=34) and 80 pg (D; 50%, n=24) of McerP-BMP4 showed a concentration dependent increase in head truncation. (G-I) A progressive head reduction and loss of eye were observed when 20 pg (I; 100%, n=26), 40 pg (H; 24%, n=21) and 80 pg (G; 59%, n=34) of McerP-Xnr1. (J-L) Increasing the amount of McerP-Xwnt8 from 20 pg (L; 60%, n=25) to 40 pg (K; 62%, n=28) to 80 pg (J; 74%, n=19) resulted in loss of cement gland and cyclopia and ultimately in complete truncation of the head. (M,N) Synergistic effect of McerP-BMP4, Xnr1 and Xwnt8 is shown by the coinjection of 8 pg (N; 65%, n=23) and 20 pg (M; 63%, n=46) of each construct which resulted in more severe defects than the ones observed in embryos injected with equal amounts of the individual constructs (F,I and L). 20 pg of McerP-lacZ was coinjected to access the correct targeting of the promoters to the ADE (yellow arrowheads in E, H and K).

Image published in: Silva AC et al. (2003)

Copyright © 2003. Image reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

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