Nucleotide substitution: A?T.
Amino acid replacement: K181term.
The premature stop codon is in the third exon.
Amino acid replacement: ?181term.
A15133288T
A?T
K181term | drd-PA
K181term
decreased body size (with drd1)
female sterile (with drd1)
fertile (with drdCB6275-3)
lethal (with drdCB6275-3)
short lived (with drd1)
In drdlwf homozygous females and hemizygous males the midgut and cardia are severely distended and lack a peritrophic membrane. Alongside, the presence of holes in the brain indicate signs of neurodegeneration.
Approximately 50% of mutant adults have larger crops than wild-type controls.
After 22-24 hours on dyed food, the mutant adults have less dye in their midguts than wild-type controls.
Nearly 50% of mutant flies do not eat after 48 hours of starvation. For flies that do eat, there is no significant transfer of food to the midgut over the 90-minute duration of the experiment (in contrast, wild-type flies show a steady increase in midgut staining starting 15 minutes after the beginning of feeding with dyed food under these conditions). The mutant flies show a gradual increase in crop volume over the 90 minutes, in contrast to wild-type flies which show a decrease in crop volume.
Mutant and wild-type flies starved on agar have a median survival of 3 days, with no significant difference between the survival curves of both genotypes. Mutant flies kept on instant food or cornmeal-molasses food show show an increase in survival compared to mutant flies starved on agar, but show reduced survival compared to control flies kept on instant food or cornmeal-molasses food.
Mutant males and females show a significantly higher rate of spontaneous crop contraction compared to controls.
drdlwf flies are short-lived and display abnormal digestive function. Mutant flies frequently have a 'bloated' appearance; this is due to the accumulation of large amounts of liquid in the crop. drdlwf males have more than a four-fold increase in crop volume compared with wild-type males. Homozygous females have a nearly three-fold increase compared with heterozygotes.
drdlwf mutant flies display a significantly reduced rate of defecation. No accumulation of food is observed in any portions of the gut other than the crop.
The lethality observed in drdlwf flies appears to be confined to adult flies. No gross abnormalities are observed in either the survival of mutants through pre-adult development or the timing of such development.
drdlwf mutants are smaller than wild-type flies. The mean mass on the day of eclosion of drdlwf males and homozygous females is 25-30% smaller than wild-type males and heterozygous females, respectively.
drdlwf females are sterile. They lay very few eggs and no larvae appear from crosses with drdlwf homozygous females. Homozygous drdlwf ovaries contain significantly fewer egg chambers that have undergone vitellogenesis compared with heterozygotes. Indeed, mutant flies, on average, have less than one yolk-containing egg chamber in each ovary.
Starvation of drdlwf heterozygous females results in a significant disruption of oogenesis.
drdlwf/drd1 transheterozygous females are short-lived, sterile, have a smaller body mass, and fewer vitellogenic egg chambers than drd1/+ heterozygotes.
drdlwf/drdCB6275-3 transheterozygotes exhibit an increase in crop volume compared to wild-type.
drdlwf/drd1 transheterozygotes exhibit an increase in crop volume compared to wild-type.
drdlwf/drdCB6275-3 transheterozygotes exhibit a smaller number of vitellogenic egg chambers compared to wild-type.
drdCB6275-3/drdlwf females do not have a lower body mass than there siblings and are fertile.
Mutant flies begin dying 2-3 days post-eclosion and show 100% lethality within 7 days. By the time they die, lwf1 flies exhibit distended crops, suggesting that they are able to eat. However, little food appears to move into and through the midgut and hindgut, as lwf1 males show an 80% reduction in the production of fecal spots compared to wild-type flies, during the second and third days of adult life.
lwf1/lwfCB6275-3 flies display 80% mortality within 7 days post-eclosion.
drdlwf is rescued by drdUAS.cSa/Scer\GAL4DJ626
drdlwf is rescued by Scer\GAL4Act5C.PI/drdUAS.cSa
drdlwf is rescued by drdUAS.cSa/Scer\GAL4hs.PB
drdlwf is partially rescued by Scer\GAL4DJ717/drdUAS.cSa
drdlwf is partially rescued by drdUAS.cSa/Scer\GAL4hs.PB
Expressing drdUAS.cSa under the control of Scer\GAL4drd-MI15121-TG4.1 (the intrinsic Gal4 driver of drdMI15121-TG4.1) rescues adult mortality in drdMI15121-TG4.1/drdlwf flies.
Expressing drdUAS.cSa under the control of Scer\GAL4DJ626 rescues adult mortality, the presence of holes in the brain, peritrophic membrane formation and defecation rates in drdlwf/drdlwf adult flies.
Expressing drdUAS.cSa under the control of Scer\GAL4DJ717 rescues the presence of holes in the brain, partially rescues adult mortality and fails to rescue peritrophic membrane formation and defecation rates in drdlwf/drdlwf adult flies.
Limiting expression of drdUAS.cSa under the control of Scer\GAL4hs.PB to metamorphosis by exposing pupae to the permissive temperature rescues adult mortality, but not peritrophic membrane formation in drdlwf/drdlwf adult flies.
The short lived phenotype seen in drdlwf animals is rescued by expression of drdScer\UAS.cSa under the control of Scer\GAL4Act5C.PI.
Temperature shift experiments using flies carrying drdScer\UAS.cSa and Scer\GAL4hs.PB indicate that expression of drdScer\UAS.cSa during the final 48 hours of metamorphosis completely rescues the short lived phenotype seen in drdlwf animals.