74bp deletion between bases 823 and 898. This causes a frameshift and introduces a stop codon within the first zinc finger motif.
74bp deletion which causes a frameshift and introduces a stop codon within the first zinc finger motif. The position of the mutation on the reference sequence was inferred by a FlyBase curator.
A small percentage of embryos laid by grauQF31/Df(2R)Pu-D17 females develop into adult flies.
Only 2.6-3.0% of embryos derived from homozygous females progress through meiosis and develop.
Transmission rate of Dp(1;f)J21A through females to progeny is 28%, grau mutation has no effect on transmission. Mutation has no effect on Dp(1;f)J21A transmission in males.
Females lay eggs that arrest in meiosis II, the earliest defect is in anaphase I. Premature sister chromatid separation does not rescue the meiotic defects, as shown in mei-S3321 double mutants. Male meiosis and mitosis are normal.
Eggs derived from homozygous females initiate development and cytoplasmic clearing occurs in a narrow zone around the egg periphery (in wild-type embryos this process is coupled to the arrival of the nuclei at the periphery). The eggs do not seem to develop beyond this stage; pole cells are not formed and cellularisation does not occur. However, about two hours after cytoplasmic clearing, the egg periphery starts to show local contractions, in what might be an attempt at gastrulation. These contractions eventually lead to eggs which typically have one or two condensed yolk balls surrounded by more transparent cytoplasm.
Df(2R)Pu-D17/grauQF31 has lethal | maternal effect phenotype, enhanceable by cortQW55/cort[+]
Df(2R)Pu-D17/grauQF31 has lethal | maternal effect phenotype, enhanceable by cortRH65/cort[+]
grauQF31 has abnormal meiotic cell cycle | recessive phenotype, suppressible by cort+t2.7
grauQF31 has lethal | recessive | maternal effect | embryonic stage phenotype, suppressible by cort+t2.7