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. Author manuscript; available in PMC: 2018 Jan 10.
Published in final edited form as: Cell Rep. 2017 Jan 10;18(2):545–556. doi: 10.1016/j.celrep.2016.12.034

Figure 1. Opposing roles of RP paralogs, Rpl22 and Like1, in regulating gastrulation.

Figure 1

(A,B) One-cell stage zebrafish embryos were injected with translational-blocking Like1-A-MO (2ng), L22-A-MO (6ng) or both (D-MOs), following which effects on gastrulation were assessed. The images of embryos represent lateral views at 10hpf. The red and black lines indicate the anterior and posterior ends of the body axis, respectively. The angle (θ), which defines the degree of extension, was measured between the red arrow and dashed black line, and is represented graphically as the mean ± standard deviation (S.D.). Control (black); Like1 MO (red); Rpl22 MO (yellow); and double-morphants (D-MO; green). Triplicate samples were quantified and the mean ± S.D. is depicted graphically. **, p < 0.01. (C) Imaging of notochord in Like1 morphants (10hpf) co-injected with 100pg mCherry-CAAX mRNA at the 1-cell stage. The dorsal view, anterior is at the top. The lateral notochord boundaries are indicated by the dotted yellow lines, and the width of notochord was marked by white lines. (D,D’) Expression patterns of ntl in 10hpf Like1 morphants. Red Arrows mark changes in distribution in the images representing lateral (D) and dorsal (D’) views. (E,F) sox32 and lefty1 expression in Like1 morphants. Red Arrows indicated changes in expression or distibution. (E) 75%-epiboly stage, dorsal view. (F) lateral view, 16hpf. (G-I) Phospho-Smad2 and total-Smad2 were assessed in 10hpf (G), 16hpf (H), and 4.7hpf (I) Like1 morphants by immunoblotting. All results are representative of at least 3 experiments performed. See also Figure S1.

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