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. 2021 Mar 23;11:6607. doi: 10.1038/s41598-021-86153-x

Figure 8.

Figure 8

Loss of Fry impairs convergent extension movements and can be compensated by constitutively active hNDR1-PIF kinase. (ag) Dorsal marginal zone explants were prepared from Xenopus embryos at early gastrula stage (St. 10.5) and culture until late neurula stage (St. 19) when the elongation of the explant was evaluated. (a) Uninjected embryos. (b) Standard Control morpholino (St-MO) (15 ng) injected embryos. (c) fry-MO (15 ng) injected embryos and (d) fry-MO (15 ng) + FD + LZ mRNA (800 pg) co-injected embryos. (e) fry-MO (15 ng) + hNDR1-wt mRNA (250 pg) co-injected embryos (f) fry-MO (15 ng) + hNDR1-PIF mRNA (250 pg) co-injected embryos and (g) fry-MO (15 ng) + hNDR1-kd mRNA (250 pg) co-injected embryos. Representative explants are shown. (h) Percentage of elongation of dorsal marginal zone explants from embryos treated as indicated. Elongation was calculated as the difference between the initial and final length of the explants (St. 10.5 vs. St. 19) relative to the mean of the uninjected group (considered 100% elongation, dotted line). Each point represents a single explant. N: number of independent experiments, n: number of explants. Statistical significance was evaluated using Kruskal–Wallis test and Dunn's multiple comparisons test (****,††††p < 0.0001 and **,††p < 0.01). * represents the comparison to the uninjected group and † represents the comparison to the fry-MO injected group.