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Fig. 3. VPXvents do not interfere with mesoderm induction by activin in animal caps. Embryos were microinjected animally with lacZ (0.5 ng/blastomere), VPXvent-1(0.1 ng/blastomere) or VPXvent-2 (0.5 ng/blastomere) with or without activin RNA as indicated. Animal caps were cut at stage 8-9 and cultivated until sibling embryos reached stage 20. In this experiment, ventral control injections with both VPXvent-1 and VPXvent-2 induced more than 50% secondary axes. (A) Coinjection of VPXvent constructs does not inhibit elongation of animal caps, induced by activin (0.1 ng/blastomere; top; 100% elongation activin alone (n=17), 100% elongation VPXvent-1 + activin (n=15), 89% elongation VPXvent-2 + activin (n=18)). VPXvent constructs alone do not induce elongation of animal caps (bottom; lacZ, n=13 ; VPXvent-1, n=16; VPXvent-2, n=16). (B) VPXvent constructs do not inhibit activininduced mesodermal marker expression in animal caps. Total RNA was isolated from animal caps at stage 20 and analysed by RT-PCR for expression of marker genes indicated. Low and high activin correspond to 0.07 and 0.1 ng/blastomere.

Image published in: Onichtchouk D et al. (1998)

Copyright © 1998. 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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