embryonic gastric caecum & parasegment 3, with Scer\GAL4how-24B
embryonic gastric caecum & parasegment 7, with Scer\GAL4how-24B
eye | pupal stage, with Scer\GAL4ey.PU
head | pupal stage, with Scer\GAL4ey.PU
The wings of flies expressing ScrScer\UAS.cMa under the control of Scer\GAL4Bx-MS1096 always fail to unfold after eclosion.
Expression of ScrScer\UAS.cMa under the control of Scer\GAL4GMR.PU results in a severe rough eye phenotype.
Flies expressing ScrScer\UAS.cMa under the control of Scer\GAL4ey.PU dies as pupae or pharate adult, with no eyes and severely reduced head.
Expression of ScrScer\UAS.cMa under the control of Scer\GAL4dpp.blk1 results in transformation of the arista to tarsus.
Expression of ScrScer\UAS.cMa under the control of Scer\GAL4sca-537.4 results in a mutant phenotype in the embryonic tritocerebrum. The phenotype has a penetrance of more than 70-80%.
Animals expressing ScrScer\UAS.cMa under the control of Scer\GAL4dpp.blk1 have morphologically normal legs, while the antennae are transformed distally to a tarsus-like identity.
Expression of ScrScer\UAS.cMa under the control of Scer\GAL4lab.PH does not result in morphological defects in the tritocerebrum or any other part of the embryonic brain.
When ScrScer\UAS.cMa is driven by Scer\GAL4how-24B, repressed posterior central projections (PVs) are seen in T3 and A1 and an absent ventral oblique muscle 2 (VO2) in T2. Occasionally these animals produce ectopic anterior ventral projections (AVs) in T2 and T3 which exemplifies T1 character. Occasionally an ectopic PV is seen in T2. Midgut morphology is altered with reduced gastric caecae at parasegment 3 and occasionally a reduced first constriction. Polyps that resemble ectopic gastric caecum primordia appear to form on the second midgut chamber, but fail to develop further. Midgut morphology is also altered in parasegment 7.
When driven by Scer\GAL469B, Scer\GAL4prd.RG1, or Scer\GAL4l(3)31-1-31-1 leads to a significant loss in viability.
Scer\GAL4dpp.blk1, ScrUAS.cMa has visible phenotype, suppressible by pbUAS.EGFP/Scer\GAL4dpp.blk1
Scer\GAL4dpp.blk1, ScrUAS.cMa has arista phenotype, suppressible by pbUAS.EGFP/Scer\GAL4dpp.blk1
Scer\GAL4dpp.blk1, ScrUAS.cMa has pretarsus | ectopic phenotype, suppressible by pbUAS.EGFP/Scer\GAL4dpp.blk1
Scer\GAL4lab.PH/ScrUAS.cMa is a suppressor of embryonic tritocerebrum phenotype of lab14
Dfd16, Scer\GAL4salm-459.2, Scr4, ScrUAS.cMa has adult corpus allatum phenotype
Dfd16, Scer\GAL4salm-459.2, Scr4, ScrUAS.cMa has prothoracic gland phenotype
Addition of ScrScer\UAS.cMa to Dfd16;Scr4 double mutant embryos (under the control of Scer\GAL4salm-459.2) results in both the Mx and Lb segments forming prothoracic glands.
Co-expression of pbScer\UAS.T:Avic\GFP-EGFP suppresses the arista-to-tarsus transformation seen in flies expressing ScrScer\UAS.cMa under the control of Scer\GAL4dpp.blk1.
Expression of ScrScer\UAS.cMa under the control of Scer\GAL4lab.PH rescues the tritocerebral defects seen in lab14 embryonic brains. 36.4% of embryos show a complete rescue of the defects (taking into account that the phenotypic penetrance of the lab14 phenotype is 88.6%).