The frequencies of the mild and severe phenotypes were quantitatively evaluated as shown in Figs. 7B–D. Approximately 14% of zmsi1 KD embryos exhibited a severe phenotype in which the embryo had a very small head and tail, and insufficient formation of the eyes ( Fig. 7C). The severe group appeared to also have pericardial edema. Another 46% of zmsi1 KD exhibited a mild phenotype, in which the embryo showed a slight microcephaly

and lateral curvature of the shortened spine and fin ( Fig. 7D). In both cases, these zebrafish embryos could not swim normally and the mortality rate was higher than for the control groups ( Fig. 7E). The frequency of the microcephaly find more phenotype is shown in Fig. 7F. Representative embryos defining the normal, mild and severe phenotypes are shown in Figs. 7B–D. To confirm the reproducibility of the KD phenotype, a second MO experiment was performed, in which a 25-bp MO with a completely different sequence was used to target zmsi. The frequencies of the phenotypes were similar to the first MO KD ( Fig. 7F). To confirm the

phenotype specificity, we next performed rescue experiments with purified recombinant protein from several species (Supplementary Fig. 2A). The frequency of the microcephaly phenotype decreased with the injection of zebrafish, mouse or human Msi1 protein, which were purified via their HA-tags (Fig. 7F). A statistical analysis comparing the frequency of the rescued phenotype between the KD and rescued samples indicated that the only significant difference Inhibitor Library datasheet was in the severe phenotype MG-132 purchase group. The severe phenotype was rescued by zMsi1 injection (p = 0.003), as well as by injection of the mouse (p = 0.013) or human (p = 0.010) protein. Injection of the zMsi1 protein without MO resulted in a significant increase in whole body size by day 3 (72 hpf) compared to wild-type embryos (Supplementary Figs. 2C–E). The reason why this over-expression phenotype was not restricted to the CNS is unclear; however, the injected HA-tagged protein

was detected diffusely throughout the entire embryo. To examine the hypoplasia of the CNS, a specific marker transgenic zebrafish was used. The green fluorescent protein (GFP) transgenic zebrafish Tg(elavl3:EGFP)zf8 (Park et al., 2000), designated HuC:GFP, was used in a zmsi1 KD analysis. The HuC:GFP transgenic strain was used to observe neural tissue formation over the course of development because the expression of GFP is controlled by the promoter of a neural tissue-specific RBP, HuC ( Figs. 7G–J). In the zmsi1 KD in HuC:GFP zebrafish, a limited number of GFP positive cells were detected due to hypoplasia of the neural tissue in both the brain and spinal cord ( Figs. 7G and H). Finally, the effectiveness of the MO KD of zMsi was evaluated by anti-Msi1 immunohistochemistry using frozen sections from 48 hpf embryonic spinal cord.