Fig. 3

Fig. 3 Zebrafish clp1^R44X Homozygous Mutants Show Gross Brain Defects, Reduced Survival, and Neurodegeneration

(A) Gross morphology of WT and clp1^R44X/R44X zebrafish mutants showed misshapen head, small eyes, and curved tail (arrow), suggesting neuromotor defects. Scale bar, 500 µm.

(B) Kaplan-Meier curve showed reduced survival of clp1^R44X/R44X fish (additional allele shown in Figure S3.

(C) Progressively reduced otx2 expression in developing clp1^R44X/R44X zebrafish brains. Broad otx2 expression domain at 24 hpf was unremarkable in mutant (bracket), suggesting that initial patterning was not disrupted. From 48–72 hpf, WT fish showed expression restricted to midbrain-hindbrain organizer (bracket), whereas mutant showed weak expression, completely absent by 72 hpf (#).

(D) TUNEL-positive cells were increased in mutant at 48 hpf in both the hindbrain (arrow) and the midbrain/diencephalon (double arrow), further investigated in Figure S3.

(E) Partial rescue of the clp1^R44X/R44X phenotype with human WT, but not p.R140H CLP1, mRNA by measuring curved tail height. No difference was detected between uninjected and injected with p.R140H mRNA, whereas WT mRNA partially recovered curved tail phenotype. p <0.01, Student’s t test. Error bar, SEM.

(F) In situ for otx2 in WT, clp1^R44X/R44X, and clp1^R44X/R44X injected with human CLP1 mRNA. Human CLP1, but not CLP1^R140H, prevented the loss of otx2 expression at 48 hpf in clp1 mutants, quantified at right. n >25 embryos each condition. Scale bar, 100 µm.