When Scer\GAL4hs.PB;GATAeScer\UAS.cSa strains are raised at room temperature, all the progeny die during the first larval instar, indicating leaky expression from the Scer\GAL4hs.PB regulatory sequence. When raised at 18oC, the larvae develop normally. When the larvae are heat-shocked for 30 minutes at 30oC, and then returned to room temperature for 18 hours, they display a number of abnormalities, including melanisation of the trachea and hindgut. All of the larvae die prior to pupation.
Ectopic expression of GATAeScer\UAS.cSa in the developing fat body, salivary glands and blood, under the control of Scer\GAL4c754 results in an extensively spotted and scarred second instar larval cuticle, with melanised portions of the hindgut and excessive lamellocytes, suggesting that expression of GATAeScer\UAS.cSa causes a systemic immune response in the absence of infection.
The normal fat body is a single-layered tissue, but in response to GATAeScer\UAS.cSa expression (under the control of Scer\GAL4c754) it exhibits buckling and regions composed of multiple cell layers. In addition, nmuclei are larger than normal in these cells, suggesting an additional round of endoreplication.