TABLE 3.
Test for complementation of Df(1)Hmr− female viability and fertility defects by In(1)AB
| Genotype (no. of females at start) | Viability relative to Na (mean no. of progeny/female ± SD)b
|
||||
|---|---|---|---|---|---|
| Day 5 | Day 10 | Day 15 | Day 20 | Day 25 | |
| In(1)AB,w/Hmr1r1 | 0.90 | 0.86 | 0.82 | 0.80 | 0.68 |
| (N = 92) | (78.5 ± 14.8) | (51.6 ± 19.2) | (33.3 ± 21.1) | (10.6 ± 15.6) | (1.3 ± 4.1) |
| In(1)AB,w/Df(1)Hmr− | 0.94 | 0.87 | 0.84 | 0.75 | 0.68 |
| (N = 88) | (31.4 ± 18.4)*** | (3.9 ± 5.6)*** | (0.12 ± 0.56)*** | (0)*** | (0)* |
Single females of the indicated genotypes were mated to two wild-type males and processed as in Table 2. Crosses were done at 27°.
N dropped during the course of the experiment [to 66 at day 25 in the crosses with In(1)AB, w/Hmr1r1 and to 71 at day 25 in the crosses with In(1)AB, w/Df(1)Hmr−], primarily due to lethality of the males. The difference in the proportions of live and dead females between the w+ and w classes was tested by a one-tailed Fisher's exact test. All tests were nonsignificant (P > 0.05).
For average fertility, the difference between the w+ and w classes was tested by a one-tailed t-test. *P < 0.05; **P < 0.01; ***P < 0.001, respectively. SD, standard deviation.