Fig. 1

Fig. 1

kur Mutants Harbor Mutations in c21orf59 and Exhibit Defects Characteristic of Defective Cilia Motility

(A) Lateral views of zebrafish sibling control embryos and kur^tm304 and kur^tj271 mutants at 2 dpf and 5 dpf. At 25°C, kur^tm304 mutants exhibit early body axis defects that resolve by 5 dpf, whereas kur^tj271 mutants do not resolve their body curvatures. Both mutants exhibit kidney cysts (white arrows), but the penetrance is variable in kur^tm304/tm304 at 25°C.

(B) Embryos from kur^+/tm304 intercrosses were raised at 32°C, 28°C, or 25°C and were scored for body curvature defects at 1 dpf and 5 dpf. While abnormalities were present in around 25% of embryos at 32°C and 28°C, mutants raised at 25°C exhibited fewer incidences of axis curvature at 1 dpf and almost all mutants had recovered at 5 dpf. The total number of embryos examined was 32°C, n = 292; 28°C, n = 332; and 25°C, n = 341. Shown is the average percentage of embryos with curved body axis from four biological replicates.

(C) Fertility of kur^tm304 adult mutants was assessed by scoring the number of fertilized eggs following homozygous female crosses to heterozygous males and vice versa. Shown is the average percentage of embryos fertilized from three biological replicates.

(D) Percentage of embryos showing the indicated situs phenotypes. The embryos were processed by ISH for myl7, ins, and fkd2 to mark the heart, pancreas, and liver, respectively, at 2 dpf. The statistical comparison of different genotypes was performed using chi-square analysis with p < 0.05 being considered to report significant differences.

(E) Early somite-stage (ss) embryos were processed for immunostaining using acetylated alpha-tubulin antibodies to mark the ciliary axoneme. The confocal imaging of KV revealed the presence of cilia in sibling control embryos as well as kurtj271^tj271 mutants.

(F) Schematic diagram of C21orf59/Kur protein showing the approximate positions of the predicted CC domain and the DUF. The position and nature of the kur^tm304 (I44N) and kur^tj271 (Q225X) mutations are shown.

(G) kur expression in zebrafish embryos at the stages indicated. kur is provided maternally at the 1-cell stage (i), followed by expression in the DFCs at 50% epiboly (ii). The expression is observed in KV (iii), pictured here at the 3-ss with a close-up of KV in the inset. During somitogenesis, kur is expressed in tissues with motile cilia including the pronephros (white arrows), the floorplate of the NT (white arrowheads), and the otic vesicles (iv-vi). Expression in the pronephros at the 24-ss overlaps with MCC markers rfx2 and cetn2 (vii-ix).