Expression of olf186-FScer\UAS.cZa under the control of Scer\GAL4elav-C155 does not affect developmental rate.
The expression of olf186-FScer\UAS.cZa under the control of Scer\GAL4ppk.PG results in third instar larval class IV abdominal dorsal multidendritic ddaC neurons exhibiting abnormal dendritic terminals, as compared to controls; expression under the control of Scer\GAL4221 results in no obvious dendrite morphology defects in class I abdominal dorsal multidendritic ddaD and ddaE neurons, as compared to controls.
Overexpression of olf186-FScer\UAS.cZa in wild-type neurons (under the control of Scer\GAL4elav-C155) does not afffect SOCE and '[Ca[2+]'][[ER]], although it does elevate '[Ca[2+]'][[i]] to ~1υM in wild-type.
OraiUAS.cZa, Ras85DV12.UAS, Scer\GAL4Act5C.PI, StimUAS.cEa has neoplasia | somatic clone | larval stage phenotype, suppressible by bskDN.UAS.cUa, Scer\GAL4Act5C.PI
OraiUAS.cZa, Ras85DV12.UAS, Scer\GAL4Act5C.PI, StimUAS.cEa has neoplasia | somatic clone | larval stage phenotype, non-suppressible by BacA\p35UAS.cHa, Scer\GAL4Act5C.PI
StimUAS.cEa/OraiUAS.cZa, Scer\GAL4Act5C.PI is an enhancer of neoplasia | larval stage | somatic clone phenotype of Ras85DV12.UAS, Scer\GAL4Act5C.PI
Scer\GAL4elav-C155, StimUAS.cAa, OraiUAS.cZa is a suppressor of abnormal flight phenotype of Itprug3/Itprka1091
StimUAS.cAa, Scer\GAL4Ilp2.PR, OraiUAS.cZa is a suppressor of visible phenotype of Itprug3/Itprka1091
StimUAS.cAa, Scer\GAL4Ilp2.PR, OraiUAS.cZa is a suppressor of abnormal neurophysiology phenotype of Itprug3/Itprka1091
Scer\GAL4elav-C155, StimUAS.cAa, OraiUAS.cZa is a suppressor of abnormal neurophysiology phenotype of Itprug3/Itprka1091
StimUAS.cAa, Scer\GAL4Ilp2.PR, OraiUAS.cZa is a suppressor of abnormal flight phenotype of Itprug3/Itprka1091
OraiUAS.cZa, Scer\GAL4Ddc.PL, StimUAS.cAa has lethal | P-stage phenotype
OraiUAS.cZa, Ras85DV12.UAS, Scer\GAL4Act5C.PI, StimUAS.cEa has eye disc | somatic clone phenotype, suppressible by bskDN.UAS.cUa, Scer\GAL4Act5C.PI
OraiUAS.cZa, Ras85DV12.UAS, Scer\GAL4Act5C.PI, StimUAS.cEa has eye disc | somatic clone phenotype, non-suppressible by BacA\p35UAS.cHa, Scer\GAL4Act5C.PI
StimUAS.cEa/OraiUAS.cZa, Scer\GAL4Act5C.PI is an enhancer of eye disc | somatic clone phenotype of Ras85DV12.UAS, Scer\GAL4Act5C.PI
StimUAS.cAa, Scer\GAL4Ilp2.PR, OraiUAS.cZa is a suppressor of wing phenotype of Itprug3/Itprka1091
Scer\GAL4elav-C155, StimUAS.cAa, OraiUAS.cZa is a suppressor of wing phenotype of Itprug3/Itprka1091
Co-expression of StimScer\UAS.cAa and olf186-FScer\UAS.cZa driven by Scer\GAL4Ilp2.PR completely suppresses the wing posture, flight and flight physiology defects of Itp-r83Aka1091/Itp-r83Aug3 flies.
Simultaneous expression of StimScer\UAS.cAa and olf186-FScer\UAS.cZa driven by Scer\GAL4Ddc.PL in aminergic neurons results in pupal lethality.
Pan-neuronal expression of StimScer\UAS.cAa and olf186-FScer\UAS.cZa driven by Scer\GAL4elav-C155 in Itp-r83Aka1091/Itp-r83Aug3 flies suppresses the abnormal wing-posture to varying extents but does not fully restore flight ability.
Overexpression of olf186-FScer\UAS.cZa driven by Scer\GAL4Ilp2.PR in Itp-r83Aka1091/Itp-r83Aug3 mutant neurons fails to restore global intracellular Ca[2+] homeostasis.
Simultaneous expression of StimScer\UAS.cAa and olf186-FScer\UAS.cZa driven by Scer\GAL4Ilp2.PR in Itp-r83Aka1091/Itp-r83Aug3 mutant neurons restores global intracellular Ca[2+] homeostasis.
Overexpression of olf186-FScer\UAS.cZa in wild-type neurons (under the control of Scer\GAL4elav-C155) elevates '[Ca[2+]'][[i]] levels to ~1υM in a Itp-r83Aka1091/Itp-r83Aug3 backgrounds.
Expression of olf186-FScer\UAS.cZa in Ilp2 neurons (under the control of Scer\GAL4Ilp2.PR) partially suppresses the altered wing posture of Itp-r83Aka1091/Itp-r83Aug3 mutants. Although flight ability is not restored, flight patterns are initiated on air-puff delivery, while these are normally completely lacking in Itp-r83Aka1091/Itp-r83Aug3 mutants. Spontaneous hyperactivity of the DLMs in Itp-r83Aka1091/Itp-r83Aug3 mutants is suppressed to a significant extent by expression of olf186-FScer\UAS.cZa either ubiquitously (Scer\GAL4hs.PB at 25[o]C) or in the aminergic (Scer\GAL4Ilp2.PR) and glutamatergic subneuronal domains (Scer\GAL4OK371).
Ubiquitous expression of olf186-FScer\UAS.cZa under the control of Scer\GAL4hs.PB in Itp-r83Aka1091/Itp-r83Aug3 mutants, up-regulated by a heat shock either in 24hr pupae or in 1-day-old adults results in a significant number of flies initiating flight in response to an air puff. Thus, levels of olf186-FScer\UAS.cZa can modulate flight circuit activity both during its development and in adult function. However, the flight patterns obtained are not sustained and appear arrhythmic, indicating that although olf186-FScer\UAS.cZa overexpression can suppress the flight defects and associated physiology of Itp-r83Aka1091/Itp-r83Aug3 mutants to a significant extent, it is insufficient to regain complete flight.
Pan-neural overexpression of olf186-FScer\UAS.cZa in Itp-r83Aka1091/Itp-r83Aug3 neurons restores detectable SOCE to 70%, as in wild-type. Also, '[Ca[2+]'][[ER]] is restored to wild-type levels, indicating that reduced SOCE and elevated '[Ca[2+]'][[ER]] in Itp-r83Aka1091/Itp-r83Aug3 are linked homeostatic processes.
Overexpression of olf186-FScer\UAS.cZa in wild-type neurons (under the control of Scer\GAL4elav-C155) does not afffect SOCE and '[Ca[2+]'][[ER]], although it does elevate '[Ca[2+]'][[i]] to ~1υM in wild-type and Itp-r83Aka1091/Itp-r83Aug3 backgrounds.
Scer\GAL4ple.PF/OraiUAS.cZa partially rescues OraiEY09167
Scer\GAL4VGlut1-OK371/OraiUAS.cZa partially rescues OraiEY09167
Scer\GAL4dimm-929/OraiUAS.cZa fails to rescue OraiEY09167
Scer\GAL4Mef2.PR/OraiUAS.cZa fails to rescue OraiEY09167
The developmental delay, small body size and partial lethality of olf186-FEY09167 homozygous mutants is rescued by expression of olf186-FScer\UAS.cZa under the control of the Scer\GAL4elav-C155 driver. The lethality is also partially rescued when the expression is driven by either Scer\GAL4ple.PF or Scer\GAL4VGlut-OK371, no rescue is observed with either Scer\GAL4dimm-929 or Scer\GAL4Mef2.PR drivers.