Insertion of sequence encoding termination codons flanking a w+* marker.
Ends-out gene targeting was used to replace a segment of from the 5' end of the Bsg25D with a mini-white gene, creating a null allele.
Bsg25DNull/Bsg25DNull embryos, but not Bsg25DNull/+ embryos, exhibit a significantly decreased hatching rate, as compared to wild type. Bsg25DNull/Bsg25DNull embryos exhibit varying severities of mitotic defects, including excessive nuclear fallout, abnormal nuclear aggregates, bridges between chromosomes, chromosome segregation defects, delocalization of the centrosome from the mitotic spindle, and in some cases failure of cellularization, monopolar and tripolar spindles.
Offspring of Bsg25DNull/Df(2L)Exel6011 x Bsg25DNull/Df(2L)Exel6011 crosses exhibit a modest but significant decrease in pole cell number, as compared to controls.
Females expressing Bsg25DScer\UAS.P\T.CR.3'UTR.T:Avic\GFP-EGFP in a Bsg25DNull/Df(2L)Exel6011 background do not produce a significantly different number of eggs lacking dorsal appendages, or any significant difference in hatching frequency, as compared to controls.
Females expressing Bsg25DScer\UAS.P\T.CR.T:Avic\GFP-EGFP in a Bsg25DNull/Df(2L)Exel6011 background produce a significantly increased number of eggs lacking dorsal appendages, but no difference in hatching frequency, as compared to controls; the dorsal appendage phenotype is not seen when females express Bsg25DScer\UAS.P\T.CR.T:Avic\GFP-EGFP in a wild type background.
Females expressing Avic\GFPScer\UAS.P\T.Bsg25D.3'UTR in a Bsg25DNull/Df(2L)Exel6011 background do not produce a significantly different number of eggs lacking dorsal appendages, or any significant difference in hatching frequency, as compared to controls.