lethal, with Scer\GAL4cb01
lethal, with Scer\GAL4cb04
lethal, with Scer\GAL4cb06
lethal, with Scer\GAL4cb07
lethal, with Scer\GAL4cb08
lethal, with Scer\GAL4cb09
lethal, with Scer\GAL4cb10
lethal, with Scer\GAL4cb13
lethal, with Scer\GAL4cb15
lethal, with Scer\GAL4cb20
lethal, with Scer\GAL4cb21
lethal, with Scer\GAL4cb22
lethal, with Scer\GAL4cb24
lethal, with Scer\GAL4cb26
lethal, with Scer\GAL4cb28
lethal, with Scer\GAL4cb29
lethal, with Scer\GAL4cb30
lethal, with Scer\GAL4cb32
lethal, with Scer\GAL4cb39
lethal | female, with Scer\GAL4GMR44E10
viable, with Scer\GAL4cb03
viable, with Scer\GAL4cb05
viable, with Scer\GAL4cb11
viable, with Scer\GAL4cb12
viable, with Scer\GAL4cb17
viable, with Scer\GAL4cb19
viable, with Scer\GAL4cb23
viable, with Scer\GAL4cb25
viable, with Scer\GAL4cb27
viable, with Scer\GAL4cb31
viable, with Scer\GAL4cb34
viable, with Scer\GAL4cb35
viable, with Scer\GAL4cb36
viable, with Scer\GAL4cb37
viable, with Scer\GAL4cb38
viable, with Scer\GAL4cb40
visible, with Scer\GAL4Eq
Adulthood-specific expression of ttkp69.UAS under the control of Scer\GAL4GMR44E10 leads to females with a severely decreased egg-laying rate and significant retention of mature follicles in the ovary, as compared to controls. Consistently, follicles rupture much less frequently upon induction by OA or ionomycin, as compared to controls.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4twi.PB and Scer\GAL4how-24B leads to lethality at embryonic stages due to severe defects in the specification of all three muscle types. The heart is either completely absent or only a few isolated cardioblasts are visible, visceral musculature contains gaps and has abnormal organization, somatic musculature contains very few correctly specific and differentiated muscle fibers, with cells that remain mononucleated and form small muscles that lack clear identity.
Follicular cells expressing ttkp69.Scer\UAS under the control of Scer\GAL4e22c are reduced in size.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4lz-gal4 results in severely disrupted adult eyes that show scarring and lack ommatidial structures. In third instar larval eye discs ommatidia show reduced numbers of cone cells and R1, R6 and R7 photoreceptor cells.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4GMR.PF results in severely perturbed adult eyes, displaying no ommatidial structure. Ommatidia show reduced numbers of cone cells and R1, R6 and R7 photoreceptor cells.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4btl.PS results in impaired tracheal branch fusion.
When expression is driven by Scer\GAL4c739, ttkp69.Scer\UAS shows a mushroom body Class I phenotype; neuron number reduced. This phenotype is similar to, but less extreme than, that caused by ttkUY181 driven by Scer\GAL4c739. Loss of neurons is not accompanied by increase in number of glial cells.
When Scer\GAL4c527 is expressed under the control of Scer\GAL4c527 in third instar larvae, defects are seen in glial cell migration in the developing eye. In about 20% of these animals surface glial cells do not enter the eye disc and R cell axons fail to enter the optic stalk forming a mass of R cell axons in the basal region of the disc. In the remaining larvae, fewer surface glial cells are found in the eye disc. In these discs R cell axons project into the optic stalk, but are highly disorganised.
Flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4cb12, Scer\GAL4cb19, Scer\GAL4cb35, Scer\GAL4cb36, Scer\GAL4cb37 or Scer\GAL4cb38 are moderately viable. Flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4cb05 or Scer\GAL4cb23 are viable at 18oC.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4ey.PB results in deletion of the eye.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4dpp.blk1 affects furrow reincarnation but not birth in the eye disc.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4Eq1 results in a lack of most microchaetae.
Scer\GAL4Kr.PM-mediated expression leads to a partial block of neuronal development in the PNS and CNS. Scer\GAL4sca-537.4-mediated expression impairs neuronal differentiation. In late stage 16/17 embryos cell death is observed.
Eyes are deformed, severely reduced in size and lack bristles, cone cells and photoreceptor cells in flies expressing ttkp69.Scer\UAS under the control of Scer\GAL4GMR.PF.
Scer\GAL4GMR.PF, ttkp69.UAS has ommatidium | third instar larval stage phenotype, suppressible | partially by lzGMR.PD
Scer\GAL4GMR.PF, ttkp69.UAS has photoreceptor cell R1 | third instar larval stage phenotype, suppressible | partially by lzGMR.PD
Scer\GAL4GMR.PF, ttkp69.UAS has photoreceptor cell R6 | third instar larval stage phenotype, suppressible | partially by lzGMR.PD
Scer\GAL4GMR.PF, ttkp69.UAS has photoreceptor cell R7 | third instar larval stage phenotype, suppressible | partially by lzGMR.PD
Scer\GAL4GMR.PF, ttkp69.UAS has cone cell | third instar larval stage phenotype, suppressible | partially by lzGMR.PD
ttkp69.UAS/Scer\GAL4Eq is a suppressor of mesothoracic tergum & microchaeta | ectopic phenotype of Scer\GAL4Eq, phylUAS.cPa
Scer\GAL4sca-T3, repoUAS.cYa, ttkp69.UAS has larval neuron phenotype
Over-expression of lzGMR.PD in flies expressing ttkp69.Scer\UAS in under the control of Scer\GAL4GMR.PF partially suppresses the loss cone cells and R1, R6 and R7 photoreceptor cells.
Co-expression of repoScer\UAS.cYa and ttkp69.Scer\UAS under the control of Scer\GAL4sca-T3 results in a synergistic suppression of neuronal development in embryos.
Most notal microchaetae are missing in animals coexpressing phylScer\UAS.cPa and ttkp69.Scer\UAS under the control of Scer\GAL4Eq1.
ttkp69.UAS, Scer\GAL4twi.PB, Scer\GAL4how-24B partially rescues ttkD2-50
ttkp69.UAS/Scer\GAL4hs.PB partially rescues ttktwp/ttk1e11
ttkp69.UAS/Scer\GAL4sli.PS partially rescues ttkB330
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4twi.PB and Scer\GAL4how-24B partially rescues the muscle morphology defects of ttkD2-50 mutants.
Expression of ttkp69.Scer\UAS under the control of Scer\GAL4btl.PS in ttkD2-50 mutant animals rescues the tracheal intercalation defects. Terminal branch fusion defects of the lateral trunk are also rescued in these animals.
Short heat shocks and moderate temperatures in ttktwp/ttktwp, ttkp69.Scer\UAS Scer\GAL4hs.PB animals lead to significant partial rescue of dorsal appendage and chorion defects. Eggs are normal in shape and size and dorsal appendages are significantly longer than seen in the mutants alone. Longer heat shocks lead to a dramatic decline in rescue frequency accompanied by an increase in defects early in oogenesis.
Scer\GAL4sli.PS-mediated expression partially rescues the CNS phenotype with two copies of the construct.