UAS regulatory sequences drive expression of a mutant form of Pka-R1 that contains a mutation in a cAMP binding site (amino acid replacement G321D). This mutant regulatory subunit acts as an inhibitor of protein kinase A (PKA) activity; although the subunit can be activated in vitro by cAMP, it requires cAMP concentrations higher than those likely to be seen in vivo.
cuticle, with Scer\GAL4E62-2
wing, with Scer\GAL4C166-2
wing, with Scer\GAL4E62-2
wing, with Scer\GAL4h-1J3
There is a significant increase in average miniature excitatory junctional current (mEJC) amplitude in larvae carrying Pka-R1BGD.Scer\UAS expressed under the control of Scer\GAL4hs.PB in a Df(2L)γ15 background even in the absence of heat shock, when compared to wild-type larvae. There is a further significant increase in average mEJC amplitude when the larvae are heat shocked.
Partial wing duplication, cuticular outgrowth, distally truncated tarsae with multiple ectopic bristle columns.