A deletion generated by homologous recombination. The extent of the deletion was determined from reported primer sequences.
The percentage of ppk261/ppk261 or ppk26Gal4/ppk261 third instar larvae showing rolling behavior in response to 47mN nociceptive mechanical stimuli is significantly reduced compared to wild type; ppk261/ppk261 larvae show this reduction in response to a wide range of mechanical forces (2.5, 5, 12 and 47mN), but show normal response delay (similar to controls) in a 47[o]C thermal nociception assay.
ppk261 has abnormal pain response | third instar larval stage phenotype, enhanceable by PiezoKO/PiezoKO
ppk261 has abnormal pain response | larval stage phenotype, non-enhanceable by ppkΔ16
ppk261 has abnormal pain response | larval stage phenotype, non-suppressible by ppkΔ16
ppk261/ppk261 is an enhancer of abnormal pain response | third instar larval stage phenotype of PiezoKO
ppk261 is a non-enhancer of abnormal pain response | larval stage phenotype of ppkΔ16
ppk261 is a non-suppressor of abnormal pain response | larval stage phenotype of ppkΔ16
ppk261 is rescued by Scer\GAL4ppk26.PG/ppk26UAS.mCherry
ppk261 is rescued by ppk26+t6.4
ppk261 is rescued by ppk26UAS.cGa/Scer\GAL4ppk26.PG
ppk26+t6.4 or expression of ppk26Scer\UAS.cGa driven by Scer\GAL4ppk26.PG rescues rolling behavior in response to 47mN nociceptive mechanical stimuli in ppk261/ppk261 third instar larvae.