TABLE 3.
Deficiency mapping of autosomal QTL affecting abdominal bristle number
| Both sexes
|
Females
|
Males
|
||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Deficiency | P(L × G) | P(L × G × S) | Var(Df) | Var(Bal) | P(L × G) | Var(Df) | Var(Bal) | P(L × G) | Var(Df) | Var(Bal) | QTL | Sex |
| Df(2L)C144 | 0.016 | 0.326 | 3.44 | 4.13 | 0.115 | 4.19 | 4.63 | 0.028 | 3.32 | 4.01 | 23A1–2;23C3–5 | B |
| Df(2L)cl-h3 | 0.027 | 0.001 | 9.56 | 5.95 | 0.540 | 5.57 | 3.87 | 0.001 | 22.42 | 11.48 | 25D2–4;25F3–26A1 | M |
| Df(2L)XE-2750 | 0.073 | 0.037 | 1.84 | 0.52 | 0.107 | 2.79 | 0.29 | 0.017 | 1.73 | 1.06 | 28C;28D3 | M |
| Df(2L)N22-14 | 0.041 | 0.253 | 2.86 | 3.15 | 0.007 | 3.00 | 3.06 | 0.683 | 2.60 | 3.51 | 29C1–2; 30C1–2 | F |
| Df(2R)M41A4 | 0.023 | 0.028 | 0.31 | 0.77 | 0.016 | 2.86 | 0.46 | 0.085 | 0.59 | 0.64 | 41A | F |
| Df(2R)Np5 | 0.051 | 0.156 | 1.26 | 1.52 | 0.148 | 0.86 | 1.35 | 0.046 | 1.79 | 1.82 | 44F12;45A6–7 | M |
| Df(2R)B5 | 0.025 | 0.656 | 1.92 | 1.09 | 0.274 | 2.36 | 0.60 | 0.062 | 2.28 | 1.37 | 46A;46C | B |
| Df(2R)X1 | 0.115 | 0.023 | 1.24 | 1.05 | 0.007 | 2.90 | 1.53 | 0.266 | 1.58 | 1.75 | 46C;46D7–9 | F |
| Df(2R)stan1 | 0.021 | 0.737 | 1.06 | 1.05 | 0.214 | 0.56 | 0.83 | 0.043 | 2.27 | 2.24 | 46D7–9;47D3 | B |
| Df(2R)CX1 | 0.037 | 0.558 | 2.27 | 0.51 | 0.063 | 1.91 | 0.64 | 0.570 | 2.06 | 1.04 | 49E7–F1;50C23–D2 | B |
| Df(2R)Jp1 | 0.018 | 0.394 | 6.32 | 7.71 | 0.500 | 2.52 | 5.48 | 0.023 | 12.39 | 11.68 | 51D3–8;52F5–9 | B |
| Df(2R)Pcl7B | 0.030 | 0.272 | 1.63 | 1.70 | 0.129 | 0.91 | 1.38 | 0.095 | 3.62 | 1.86 | 54E8–F1;55A | B |
| Df(2R)M60E | 0.002 | 0.551 | 3.23 | 1.05 | 0.159 | 2.12 | 0.53 | 0.002 | 5.06 | 1.47 | 60E2–3; 60E6–8 | B |
| Df(3L)pbl-X1 | 0.015 | 0.776 | 3.10 | 1.32 | 0.219 | 3.27 | 1.02 | 0.162 | 2.72 | 1.51 | 65F3;66B8–9 | B |
| Df(3L)lxd6 | 0.022 | 0.997 | 4.21 | 6.54 | 0.472 | 4.28 | 6.09 | 0.442 | 3.91 | 5.45 | 67E1–2;67F2–3 | B |
| Df(3L)vin7 | 0.591 | 0.022 | 3.52 | 3.39 | 0.033 | 5.22 | 3.12 | 0.347 | 3.20 | 4.16 | 69A1–3;69B4–5 | F |
| Df(3L)brm11 | 0.011 | 0.945 | 6.22 | 2.99 | 0.182 | 6.07 | 2.05 | 0.426 | 5.68 | 3.30 | 72A1; 72D1–10 | B |
| Df(3L)st-f13 | 0.041 | 0.118 | 3.59 | 2.17 | 0.296 | 3.03 | 1.70 | 0.004 | 4.58 | 2.89 | 72D1–10;73A3 | M |
| Df(3L)VW3 | 0.009 | 0.015 | 2.66 | 3.21 | 0.024 | 3.68 | 4.49 | 0.005 | 2.97 | 3.29 | 76A3;76B1–2 | F, M |
| Df(3R)D8 | 0.033 | 0.904 | 6.31 | 3.14 | 0.196 | 7.16 | 3.88 | 0.323 | 5.71 | 2.64 | 84D11–14;85A2 | B |
| Df(3R)M-Kx | 0.288 | 0.011 | 3.39 | 4.53 | 0.010 | 4.61 | 5.84 | 0.243 | 2.81 | 4.18 | 86E2–4;87B1–5 | F |
| Df(3R)T-32 | 0.423 | 0.011 | 3.08 | 3.52 | 0.030 | 3.90 | 4.41 | 0.938 | 3.12 | 2.93 | 86E2–4;87B1–5 | F |
| Df(3R)Tl-P | 0.014 | 0.786 | 4.13 | 2.55 | 0.078 | 3.97 | 3.19 | 0.281 | 3.74 | 1.83 | 97A;97E3 | B |
P-values are from the line × genotype and line × genotype × sex terms in deficiency complementation ANOVAs. Var(Df) and Var(Bal) are among-line variance components for mutation-accumulation selection lines as hemizygotes against deficiencies and heterozygotes against balancer chromosomes, respectively.