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. 2018 Oct 17;7:e38675. doi: 10.7554/eLife.38675

Figure 8. daf-22 is required for fitness differences of N2 and N2glb-5,npr-1.

Figure 8.

(a) Competition experiments between indicated strains. daf-22 encodes a sterol carrier protein, which is required for biosynthesis of most ascaroside pheromones. Red indicates the strain contain a deletion that spans the gene. **p<0.01 by Wilcoxon-Mann-Whitney nonparametric test. (b) Number of animals that carry fertilized eggs at the indicated timepoints. p=6.61×10−4 by Friedman test. (c) On plate feeding assays of the indicated strains. NS, not significant, ***p<0.001 by ANOVA with Tukey’s Honest Significant Difference test. (d and e) Attempts to rescue the relative food intake and reproductive timing defects of the daf-22 strain using crude pheromone. Neither of two concentrations of crude pheromone isolated from animals grown in liquid cultures had a significant effect on the two traits. NS, not significant, ***p<0.001 by ANOVA with Tukey’s Honest Significant Difference test. p=7.45×10−6 by Friedman test.

Figure 8—source data 1. Competition experiment between indicated strains shown in Figure 8a.
DOI: 10.7554/eLife.38675.049
Figure 8—source data 2. Number of animals observed with fertilized eggs in their uterus shown in Figure 8b.
DOI: 10.7554/eLife.38675.050
Figure 8—source data 3. Food consumption assay of indicated strains shown in Figure 8c.
DOI: 10.7554/eLife.38675.051
Figure 8—source data 4. Number of animals observed with fertilized eggs in their uterus in different pheromone concentration shown in Figure 8d.
DOI: 10.7554/eLife.38675.052
Figure 8—source data 5. Food consumption assay in different pheromone concentration shown in Figure 8e.
DOI: 10.7554/eLife.38675.053