FlyBase curator comment: this entry represents a transgenic construct where the particular construct used cannot be determined.
Under ad libitum nutrition, the adulthood-only expression of hhUAS.cUa under the control of Scer\GAL4bab1-Pgal4-2 (and Gal80[ts] for temporal control of expression) leads to excessive or disorganized basal stalk cells, mis-shaped follicle cells and/or multilayering of the follicular epithelium, as compared to controls. Under starvation, this expression leads to a significant increase in mitotic index of the follicular epithelium, but leads to a less severe multilayering phenotype, as compared to controls.
Compared to controls unresponsive to a 38[o]C probe (without pre-exposure to UV), early third instar larvae with expression of hhScer\UAS.cUa driven by Scer\GAL4ppk.1.9 (but not Scer\GAL4A58 or Scer\GAL4Myo31DF-NP0001) show significant withdrawal responses (genetic allodynia).
In wild type third instar larvae, two dorsal tracheal branches fuse to give rise to two terminal cells with multiple branches; a significantly increased percentage of Scer\GAL4btl.PU>hhScer\UAS.cUa mutant terminal branches have excess (>2) terminal cells.
Scer\GAL4ppk.1.9, hhUAS.cUa has abnormal pain response | early third instar larval stage | heat sensitive phenotype, suppressible | partially by dispGD2813/Scer\GAL4ppk.1.9
Scer\GAL4kn-col85-GAL4/hhUAS.cUa is a suppressor | partially of lamellocyte | larval stage phenotype of Scer\GAL4kn-col85-GAL4, hecaGD8578
Co-expression of dispGD2813 significantly suppresses the withdrawal responses to a 38[o]C probe (without pre-exposure to UV) seen in early third instar larvae with hhScer\UAS.cUa over-expressed by Scer\GAL4ppk.1.9.