UASt regulatory sequences drive expression of an inverted repeat.
Garland cells expressing Rab7GD11800 under the control of Scer\GAL4pros.PU show enlarged late endosomes and abnormal lysosomes.
Adulthood-only expression of Rab7GD11800 under the control of Scer\GAL4esg.PU leads to a significant increase in the number of mitotic cells (phospho-H3 staining) in the adult midgut, as compared to controls. (The temporal regulation of expression is dependent on Gal80[ts] and induced by temperature shift to 29[o]C for 5-6 days during adulthood).
Expression of Rab7GD11800 under the control of Scer\GAL4Act.PU in clones of larval fat body cells prevents formation of autolysosome.
Animals expressing Rab7GD11800 under the control of Scer\GAL4grh.D4 are viable, no obvious defects in larval dorsal trunk elongation and airway morphology are observed and the larvae are of comparable size to age-matched controls.
The adulthood-only expression of Rab7GD11800 under the control of Scer\GAL4esg-NP5130 (and Gal80[ts], for the temporal control of expression) leads to a significant increase in the numbers of both intestinal stem cells and enteroblasts in the adult midgut, as compared to controls.
Expression of Rab7GD11800 under the control of Scer\GAL4hh-Gal4 or Scer\GAL4ptc-559.1 results in an enlarged endosome phenotype.
Expression of Rab7GD11800 under the control of Scer\GAL4hh-Gal4 in the posterior compartment of the wing disc results in an increase in perimeter of the multivesicular bodies in the posterior compartment compared to those in the anterior compartment.
Primary macrophages isolated from animals expressing Rab7GD11800 under the control of Scer\GAL4Pxn.PS have an similar number of F-actin rich protrusions to wild type.
Expression of Rab7GD11800 under the control of Scer\GAL4da.G32 results in a glial overmigration phenotype in the eye disc.
Expression of Rab7GD11800 under the control of Scer\GAL4repo.PU or Scer\GAL4ey.3.5.Exel has no effect on glial cell migration in the eye disc.
Adults expressing Rab7GD11800 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.
Depending on the insertion line used, expression under the control of Scer\GAL4Mef2.PR can result in lethality by 7 days after eclosion.
Rab7GD11800, Scer\GAL4esg.PU has increased occurrence of cell division | adult stage phenotype, suppressible by Rab11JF02812, Scer\GAL4esg.PU
Scer\GAL4nSyb.PU/Rab7GD11800 is a suppressor of abnormal neurophysiology | third instar larval stage phenotype of sky1/sky2
Rab7GD11800, Scer\GAL4esg.PU has adult midgut epithelium phenotype, suppressible by Rab11JF02812, Scer\GAL4esg.PU
Rab7GD11800, Scer\GAL4Act.PU is a suppressor | somatic clone of embryonic/larval fat body | somatic clone | larval stage phenotype of Rab2Q65L.UASp.YFP, Scer\GAL4Act.PU
Rab7GD11800, Scer\GAL4Act.PU is a suppressor | somatic clone of autophagosome | somatic clone | larval stage phenotype of Rab2Q65L.UASp.YFP, Scer\GAL4Act.PU
Scer\GAL4hh-Gal4/Rab7GD11800 is a suppressor of phenotype of l(2)gd1d7
The formation of abnormally large autophagic structures in the clones of larval fat body cells expressing Rab2Q65L.Scer\UAS.P\T.T:Avic\GFP-YFP under the control of Scer\GAL4Act.PU is prevented by co-expression of Rab7GD11800.
The increase in excitatory junctional current amplitude at the neuromuscular junction which is seen in sky1/sky2 larvae is suppressed if they are also expressing Rab7GD11800 under the control of Scer\GAL4nSyb.PU. However, the increased synaptic vesicle trafficking to endosomes seen at the neuromuscular junction in the sky1/sky2 larvae is not suppressed.
Scer\GAL4hh-Gal4-mediated expression of Rab7GD11800 suppresses the ectopic N activation phenotype (ectopic expression of wg) in the posterior of l(2)gd1d7 wing discs.
Expression of Rab7GD11800 does not suppress the ectopic N activation phenotype in shrb4 follicle cell clones.