TrpmlUAS.cVa/Scer\GAL4Hml.Δ is a suppressor | partially of abnormal immune response | recessive | adult stage phenotype of ClC-b1
TrpmlUAS.cVa, Scer\GAL4Tub.PU is a non-suppressor of lethal - all die during P-stage phenotype of AMPKαJF01951, Scer\GAL4Tub.PU
TrpmlUAS.cVa/Scer\GAL4Tub.PU is a non-suppressor of lethal - all die during P-stage | recessive phenotype of AMPKα1
TrpmlUAS.cVa/Scer\GAL4Tub.PU is a non-suppressor of lethal - all die during P-stage | recessive phenotype of AMPKα3
The late pupal lethality observed in animals expressing AMPKαJF01951 under the control of Scer\GAL4tub.PU cannot be rescued by co-expression of TrpmlScer\UAS.cVa.
The pupal-stage lethality of either hemizygous AMPKα1 or AMPKα3 males cannot be rescued by expression of TrpmlScer\UAS.cVa under the control of Scer\GAL4tub.PU.
TrpmlUAS.cVa/Scer\GAL4repo partially rescues Trpml1
TrpmlUAS.cVa/Scer\GAL4Cg.PA partially rescues Trpml1
TrpmlUAS.cVa/Scer\GAL4c754 partially rescues Trpml1
TrpmlUAS.cVa/Scer\GAL4Hml.PG partially rescues Trpml1
TrpmlUAS.cVa/Scer\GAL4Mef2.PR fails to rescue Trpml1
TrpmlUAS.cVa/Scer\GAL4e22c fails to rescue Trpml1
Ectopic expression of TrpmlScer\UAS.cVa using either the Scer\GAL4elav-C155 or the Scer\GAL4C164 driver (but not the Scer\GAL4Mef2.PR driver) rescues the loss of neuromuscular junction boutons characteristic for Trpml1 mutant third instar larvae.
Expression of trpmlScer\UAS.cVa under the control of Scer\GAL4repo partially rescues the lethality of trpml1 animals. The climbing ability of trpml1 animals is significantly rescued, but there is still some age-dependent decline in climbing ability in the rescued animals. The defects in excitatory junctional potential amplitude
of trpml1 larvae are also rescued. The accumulation of late apoptotic/necrotic cells that is seen in 21 day old trpml1 adult brains is rescued, but the accumulation of early apoptotic cells in these brains is not rescued.
Expression of trpmlScer\UAS.cVa under the control of Scer\GAL4Cg.PA rescues the lethality of trpml1 animals. The climbing ability of trpml1 animals is significantly rescued, but there is still some age-dependent decline in climbing ability in the rescued animals. The accumulation of late apoptotic/necrotic cells that is seen in 21 day old trpml1 adult brains is rescued, but the accumulation of early apoptotic cells in these brains is not rescued.
Expression of trpmlScer\UAS.cVa under the control of Scer\GAL4c754 rescues the lethality of trpml1 animals. The defects in excitatory junctional potential amplitude
of trpml1 larvae are also rescued.
Expression of trpmlScer\UAS.cVa under the control of Scer\GAL4Hml.PG partially rescues the lethality of trpml1 animals.