Imprecise excision of P{EPgy2}goeEY01697 resulting in the deletion of a 92 bp segment encompassing a 63 bp upstream genomic sequence and part of exon 1 including the transcriptional start site of goe.
Inferred boundaries of a 92 bp deletion resulting from the imprecise excision of P{EPgy2}goeEY01697, which removes 63 bp upstream of goe transcription start site and part of the first exon.
Ovaries in third instar goe5-11/goe331 larvae display an approximately 1.5-fold increase in the number of differentiating germ cells compared with wild-type. Compared with wild-type, he number of undifferentiated primordial germ cells (PGCs) remains unchanged in goe5-11/goe331 ovaries, resulting in a net increase in the total number of germ cells. Neither the mitotic index of PGCs nor the apoptotic profile show any detectable changes in goe5-11/goe331 ovaries compared to wild-type. The mutant ovaries show an increase in the number of germline cysts undergoing dedifferentiation.
goe5-11/goe331 has female germline cell | third instar larval stage phenotype, enhanceable by aos[+]/aosΔ7
aos[+]/aosΔ7, goe5-11/goe331 has female germline stem cell phenotype
aosΔ7 dominantly enhances the increased differentiating germ cell phenotype in goe5-11/goe331 mutant larval ovaries.
While neither goe5-11/goe331 nor aosΔ7/+ ovaries exhibit a remarkable reduction in the number of germline stem cells (GSCs) at white pupal stage, establishment is severely impaired in goe5-11/goe331; aosΔ7/+ ovaries. This reduction in GSC number is likely the result of an insufficient primordial germ cell pool, because both ovariole formation and niche development occur normally in goe5-11/goe331; aosΔ7/+ ovaries.
goe5-11/goe331 is rescued by Scer\GAL4VP16.nanos.UTR/goeUAS.cMa
goe5-11/goe331 is rescued by Scer\GAL4VP16.nanos.UTR/goeUAS.Tag:FLAG