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Xenbase Image ID: 132957


FIG. 2. Phenotypic consequences of Pcl1 and other Polycombgroup overexpression. Embryos were symmetrically injected in both blastomeres near the dorsal marginal zone at the four-cell stage with 0.4 ng RNA (A–F). Control (A) and mPcl1 (B–F) embryos are shown at stage 40. Eyes are small (B, C), absent (D, E), and occasionally fused (F) and embryos show characteristic changes in head shape relative to controls. Four-cell embryos were bilaterally injected with control (b-galactosidase) or mPcl1 RNA, sectioned at Stage 36 (transverse), and stained with hematoxylin– eosin (G). Note how Pcl1 markedly decreases the size of the ventricle (v) and expands the surrounding neural tissue. The positions of the eye (e) and otic vesicle (o) are indicated. PcG proteins produce similar anterior neural defects (H). Embryos were injected bilaterally at the four-cell stage with 1 ng of each RNA. At Stages 36–42 embryos were scored (H) for the distinctive changes in head morphology and eye size shown in (B–F). At least 30 embryos were analyzed for every condition in each experiment. Values are the average of three or more separate experiments. Error bars show SEM. Injected RNAs are control (b-galactosidase), Xenopus and mouse Pcl1, M33 (mouse Polycomb1), XBmi-1, and mPh2 (mouse polyhomeotic 2).

Image published in: Yoshitake Y et al. (1999)

Copyright © 1999. Image reproduced with permission of the Publisher, Elsevier B. V.

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