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XB-IMG-131533

Xenbase Image ID: 131533


Fig. 2. Loss of Xvent gene function induces secondary embryonic axes. Embryos at the 4- to 8-cell stage were microinjected (A-D) radially or (E-L) ventrally with the RNAs indicated. The amount of RNA in ng/blastomere is given in parenthesis. Microcephaly caused by microinjection of (A) EveXvent-1 (0.1) (47%, n=62) or (B) EveXvent-2 (0.1) (46%, n=67). Embryos microinjected with control construct mRNA EveXvent-1(fs) (0.25) were normal (n=44). Microcephalic phenotypes caused by wild-type mRNA injections of (C) Xvent-1 (0.15) and (D) Xvent-2 (1) are shown for comparison. Secondary axis formation resulting from injections of (E) VPXvent-1 (0.1) and (F) VPXvent-2 (0.5). Rescue of secondary axis formation by mRNA (G) coinjection of VPXvent-1 (0.1) and Xvent-1 (0.15) as well as (H) coinjection of VPXvent-2 (0.5) and Xvent-2 (1). (I) Embryos microinjected with Xvent-1P(40) (2.5) mRNA are normal. (J) Embryo microinjected with Xvent-2P(40) (2.5) showing secondary embryonic axis. (K) Normal embryo resulting from mRNA injection of control construct VPXvent-1(fs) (0.5). (L) Rescue of secondary axis formation by mRNA coinjection of Xvent-2P(40) (2.5) and Xvent-2 (1).

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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