Deletion of the Bug22 gene.
Mutant adults have a reduced lifespan which varies from a few hours to up to a few days. Both non-inflated wings and an upheld wing phenotype are seen. Many of the mutant adults have an uncoordinated phenotype, showing slowness and strongly diminished climbing ability compared to controls. More severely affected individuals have a "slimy" body wall and cannot stand upright, dying within a few hours of eclosion.
Mutant males have normal reproductive system morphology, but the seminal vesicles are empty. Spindle morphology and chromosome segregation during the meiotic divisions are normal and onion-stage spermatids are indistinguishable from wild type. The centrioles of primary spermatocytes are significantly longer than normal and centriole pairs sometimes show defects in their arrangement. The length of the basal body in elongated spermatids is significantly longer than normal and their flagella are immotile, thicker than normal and have cytoplasmic bulges.
Individualisation complexes (ICs) are correctly assembled at mutant spermatid nuclei, as in wild type. The ICs migrate away from the nucleus, but they appear dispersed and lagging along the sperm tails compared to wild type. The cystic bulge and waste bags are smaller than normal.
Post-elongation cysts in the mutant testis are disorganised, contain large amounts of cytoplasm and large membrane delimited non-electron dense inclusion bodies can be seen (not seen in wild type). The axonemes are well assembled (containing the 9+9+2 microtubule arrangement) in the mutant sperm in pupae and adults, but axonemes that appear slightly or completely opened are seen in 16.8% of adult cysts. 45.6% of late-elongation or individualising mutant cysts contain a few sperm tails with a reduced number of mitochondrial derivatives (two axonemes sharing a single major mitochondrial derivative is often seen).
Bug22KO, TTLL3BUbi.GFP has partially lethal - majority die phenotype
Bug22KO, TTLL3BUbi.GFP has abnormal developmental rate phenotype
Bug22KO, TTLL3BUbi.GFP has some die during pupal stage phenotype
Bug22KO has sperm individualization complex phenotype, enhanceable by TTLL3BUbi.GFP
Flies expressing TTLL3BUbi.T:Avic\GFP in a Bug22KO background show delayed development, and most animals die at late pupal stages or just after eclosion. The spermatogenesis defects seen in Bug22KO males are aggravated in the double mutant flies: individualisation complex recruitment and migration are severely disturbed and nuclei are dispersed along the sperm tails.
Bug22KO is partially rescued by Bug22Ubi.GFP
Bug22KO is partially rescued by Bug22UAS.GFP/Scer\GAL4JO15
Bug22KO is partially rescued by Bug22UAS.GFP/Scer\GAL4DJ684
Bug22KO is partially rescued by Bug22UAS.GFP/Scer\GAL4elav.PLu
Bug22KO is not rescued by Bug22UAS.GFP/Scer\GAL4Mef2.PR
Bug22KO is not rescued by Bug22UAS.GFP/Scer\GAL4how-24B
Expression of Bug22Scer\UAS.T:Avic\GFP under the control of either Scer\GAL4Mef2.PR or Scer\GAL4how-24B fails to rescue any aspect of the Bug22KO wing and uncoordinated phenotypes.
Expression of Bug22Scer\UAS.T:Avic\GFP under the control of Scer\GAL4JO15 partially rescues the Bug22KO wing phenotype, but the rescued animals still show defects in locomotion and climbing ability.
Expression of Bug22Scer\UAS.T:Avic\GFP under the control of either Scer\GAL4DJ684 or Scer\GAL4elav.PLu almost completely rescues the wing and uncoordinated phenotypes of Bug22KO flies.
Expression of Bug22Ubi.T:Avic\GFP almost completely rescues the wing and uncoordinated phenotypes of Bug22KO flies.