UASt regulatory sequences drive expression of an inverted repeat.
When fed on a low carbohydrate diet (0% sucrose supplement), a moderate developmental delay is observed for Scer\GAL4Cg.PA Glo1GD12888 (plus Dcr-2Scer\UAS.cDa) animals. This delay is slightly prolonged when fed a sucrose supplemented diet.
Cell size within MARCM clones expressing only Glo1GD12888 is insensitive to sucrose supplementation.
Adults expressing Glo1GD12888 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.
Expression under the control of Scer\GAL4pnr-MD237 results in bristle morphology defects on the notum in 50-60% of the Scer\GAL4pnr-MD237 expression domain.
Expression under the control of Scer\GAL4pnr-MD237 results in the absence of 10-20% of the Scer\GAL4pnr-MD237-expressing area of the notum.
Glo1GD12888, Scer\GAL4Cg.PA has abnormal developmental rate | nutrition conditional phenotype, enhanceable by FASN1GD14739, Scer\GAL4Cg.PA
Glo1GD12888, Scer\GAL4Cg.PA is an enhancer of abnormal developmental rate | nutrition conditional phenotype of FASN1GD14739, Scer\GAL4Cg.PA
Df(2L)FASNΔ24-23, Glo1GD12888, Scer\GAL4Act5C.PP has decreased cell size | somatic clone phenotype
FASN1GD14739, Glo1GD12888, Scer\GAL4Cg.PA has lethal | nutrition conditional phenotype
Df(2L)FASNΔ24-23, Glo1GD12888, Scer\GAL4Act5C.PP has nucleus | somatic clone phenotype
Animals co-expressing Glo1GD12888 and FASN1GD14739 (plus Dcr-2Scer\UAS.cDa) via Scer\GAL4Cg.PA exhibit a high rate of larval lethality and developmental delay that dramatically increases concurrently with sucrose concentration.
Cells within Df(2L)FASNΔ24-23 MARCM clones expressing Glo1GD12888 (plus Dcr-2Scer\UAS.cDa) exhibit an extreme size reduction accompanied by a severe decrease in nucleus size in larvae fed a low carbohydrate diet. Furthermore, these clonal cells cannot be observed when larvae were fed 20% sucrose supplemented diet, suggesting that these cells are eliminated during development.