FIGURE

Fig. 4

ID
ZDB-FIG-220204-19
Publication
Wong et al., 2021 - Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen storage-associated mitochondriopathy
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Fig. 4

(A) Exon-intron structure of the C2orf69 ortholog in zebrafish. Annotations of the two distinct germline frameshift mutations generated by CRISPR-Cas9 editing at the genome and protein levels. (B) Developmental expression of C2orf69 during early zebrafish embryogenesis. The transcription of C2orf69 begins at 48 hpf without any detectable maternal contribution. (C) C2orf69 KO fish are indistinguishable from WT siblings at 4 months. (D) C2orf69 KO fish show statistically significant reduced body mass and length at 8 months. (E) Spontaneous seizures in adult 8-month-old KO fish lead to fully penetrant lethality. (F) Six representative swimming tracks extracted from 2 min videos of 11 dpf KO and WT larvae each show high-speed swimming bouts (red) within 5 min of exposure to 5 mM PTZ. (G) Quantification of high-speed swim bouts in 2 min (n = 24 each). The p value of the two-sided permutation t test is <0.0001 (H) Quantification of distance swam in 2 min (n = 24 each). The p value of the two-sided permutation t test is 0.0008 (I) The percentage of KO adult fish that show tonic seizures upon exposure to 5 mM PTZ (80%) within 12 min is 2.5-fold higher compared to WT (27%). The p value of the two-sided t test is 0.03. (J) Molecular markers from 4-month-old whole brain extracts measured by qPCR reveal constitutive CNS inflammation in KO adult fish compared to WT siblings.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Am. J. Hum. Genet.