Fig. 3
- ID
- ZDB-FIG-080301-3
- Publication
- Sarmah et al., 2007 - A role for the inositol kinase Ipk1 in ciliary beating and length maintenance
- Other Figures
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Ipk1 links to IFT and microtubule-mediated organelle transport. (A and B) Codepletion of Ipk1 and either IFT88 or IFT57 synergistically perturbs LR asymmetry. (A) Embryos were injected with varying amounts of either a single MO (ipk1 MO1, ift88 MO, ift57 MO, control MO) or a MO combination (ipk1 MO1+ift88 MO, ipk1 MO1+ift57 MO, control MO+ift88 MO, control MO+ift57 MO). (B) Embryos derived from crossing either heterozygous ift88 +/- mutant or wild-type fish were injected with ipk1 MO1 or control MO. Scores for heart-tube placement defect in embryos at 28 hpf are graphed. (C and D) ipk1 knockdown perturbs microtubule-mediated organelle transport. (C) Five days after fertilization embryos [uninjected and ipk1 MO1-injected (Left)] were treated with 0.5 mg/ml epinephrine, and time (min) required for all melanosomes in the head and trunk (within the white rectangle) to become perinuclear (Center) was determined. Time required for retracted melanosomes in epinephrine-treated endpoint embryos to fully disperse on exposure to 1 mg/ml caffeine (Right) was also determined. (D) Graph of the response time for epinephrine and caffeine treatments in uninjected and ipk1 MO1 embryos. |
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Stage Range: | Prim-5 to Day 5 |