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Fig. 3. Wnt signaling cannot caudalize in the absence of Meis3 protein activity. (A) In situ hybridization of mid-late neurula embryos injected separately at the one-cell stage with either Meis3 MO (20 ng; b,f,j,n), or mWnt3 DNA (70 pg; d,h,l,p), or both (c,g,k,o). Posterior neural marker expression of HoxB3, Krox20, N-Tub and FoxD3 is highly inhibited in Meis3 morphants (b, 25/25 embryos; f, 40/40 embryos; j, 36/36 embryos; n, 16/16 embryos). mWnt3 co-expression did not rescue the expression of these markers (c, 40/41 embryos; g, 71/75 embryos; k, 63/63 embryos; o, 29/29 embryos). Ectopic mWnt3a levels alone expand posterior marker expression (d, 20/20 embryos; h, 48/49 embryos; l, 33/36 embryos; p, 18/18 embryos). (B) sqRT-PCR of pools of 18 mid-late gastrula AC explants dissected from embryos injected at the one-cell stage with mWnt3 DNA (200 pg) and BMP DNR mRNA (100 pg), and/or separately with Meis3 MO (33 ng) (n=5 experiments). (C) sqRT-PCR of pools of 18 mid-late neurula AC explants from siblings of embryos in B (n=5 experiments).

Image published in: Elkouby YM et al. (2010)

Copyright © 2010. 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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