fusome (with brwlMI05456)
oocyte (with brwlMI05456)
ovary (with brwlMI05456)
ring canal (with brwlMI05456)
brwlKG00824 is homozygous viable; heterozygotes only rarely show ovary defects.
brwlKG00824/brwlMI05456 transheterozygotes show an array of highly prevalent and progressive ovary defects, including ovariole architecture defects, egg chambers showing decreased cell division, apoptosis, loss of ring canals, mispositioned or absent oocyte, fused egg chambers and degenerated egg chambers, as compared to controls; the germaria show progressive decreases in the number of germline cells, in synaptonemal complex formation, and in the numbers of spectrosome-positive and fusome-positive cysts, as compared to controls.
brwlKG00824/brwlMI05456 has decreased cell number | oogenesis phenotype, suppressible | partially by stwlUAS.Tag:HA,Tag:FLAG/Scer\GAL4VP16.nanos.UTR
brwlKG00824/brwlMI05456 has ovary phenotype, suppressible | partially by stwlUAS.Tag:HA,Tag:FLAG/Scer\GAL4VP16.nanos.UTR
brwlKG00824/brwlMI05456 has egg chamber phenotype, suppressible | partially by stwlUAS.Tag:HA,Tag:FLAG/Scer\GAL4VP16.nanos.UTR
brwlKG00824/brwlMI05456 has oocyte phenotype, suppressible | partially by stwlUAS.Tag:HA,Tag:FLAG/Scer\GAL4VP16.nanos.UTR
The progressive oogenesis defects observed in brwlKG00824/brwlMI05456 transheterozygotes (fused egg chambers, apoptotic egg chambers, absent occyte) are delayed by the expression of stwlUAS.Tag:HA,Tag:FLAG under the control of Scer\GAL4VP16.nos.UTR.