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. 2009 Apr;181(4):1437–1450. doi: 10.1534/genetics.108.100057

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°.

a

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).

b

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.