Table 1.
Ingression depths of the anterior epidermis
| Ingression depth (μm) ± 95% CI (range; n) | ||
|---|---|---|
| Genotype | 1.5-fold | 3.0-fold |
| N2 | 2.12 ± 0.23 (1.09–3.12; 20) | 0.26 ± 0.096 (0.0–0.67; 20) |
| sym-3(mn618) | 2.39 ± 0.40 (0.81–4.24; 24) | 0.48 ± 0.56 (0.0–6.55; 22) |
| sym-4(mn619) | 2.74 ± 0.64 (0.72–5.67; 21) | 1.28 ± 1.06 (0.0–6.74; 22) |
| mec-8(u74) | 2.33 ± 0.46 (0.72–4.34; 20) | 2.42 ± 1.50 (0.0–10.43; 26) |
| mec-8; sym-3* | 4.25 ± 0.89 (2.77–5.72; 18) | 9.82 ± 0.68 (7.84–12.00; 15) |
| mec-8; sym-4 | 4.27 ± 1.16 (2.09–6.45; 16) | 9.19 ± 0.83 (7.07–10.14; 12) |
| Pha-1(tm3671) | 0.87 ± 0.18 (0.45–1.18; 16) | NA |
| mec-8; pha-1(tm3671); sym-3* | 0.83 ± 0.11 (0.40–1.19; 17) | NA |
| pha-1(e2123) | 2.15 ± 0.27 (1.04–3.34; 19) | 0.10 ± 0.07 (0.0–0.59; 16) |
| mec-8; pha-1(e2123); sym-3* | 5.27 ± 0.53 (3.89–7.46; 14) | 0.60 ± 2.35 (0.0–10.29; 19) |
| fbn-1(ns67) | 3.18 ± 0.85 (0.60–6.02; 13) | 5.34 ± 1.31 (0.0–9.24; 20) |
| fbn-1(ns67); sym-3 | 5.20 ± 0.41 (3.82–6.71; 20) | 11.73 ± 0.85 (8.59–16.34; 19) |
| fbn-1(ns67); sym-4 | 5.98 ± 0.55 (4.25–7.66; 12) | 12.84 ± 0.78 (9.65–16.37; 27) |
| mec-8; fbn-1(ns67) | 5.03 ± 0.47 (3.76–7.19; 19) | 9.84 ± 0.55 (6.94–12.24; 21) |
| fbn-1(tm290) | 6.25 ± 1.81 (0.99–12.17; 16) | 7.63 ± 3.66 (0.0–24.17; 17) |
| fbn-1(tm290); sym-3 | 5.65 ± 0.61 (2.59–7.29; 19) | 15.05 ± 1.56 (9.12–26.06; 24) |
| fbn-1(tm290); sym-4 | 5.54 ± 0.86 (3.52–9.12; 17) | 13.10 ± 1.72 (7.22–19.47; 20) |
| mec-8; fbn-1(tm290) | 9.84 ± 0.55 (5.47–15.18; 31) | NA |
Because these strains give rise to a high frequency of viable mnEx169(−) progeny in the first generation following loss of the array (F1 escapers), next-generation progeny (F2) from mnEx169(−) F1 parents were scored. NA, Non-Applicable; these genotypes led to embryonic arrest prior to the 3-fold stage.