adult thorax & macrochaeta, with Scer\GAL4pnr-MD237
Expression of hepUAS.cBa under the control of Scer\GAL4esg.PU, in combination with a Gal80[ts] transgene to restrict expression to the adult stage, results in an increase in progenitor cells and stem cell division, as well as distortion of the epithelial architecture in the gut, compared to controls; adult-stage expression under the control of Scer\GAL4NP0001 results in reduced numbers of enterocytes in the gut, but a significant increase in stem cell division and increased numbers of pre-enterocytes, compared to controls.
Expressing hepUAS.cBa under the control of Scer\GAL4ptc.PU induces some cells at the wing disc A/P boundary to delaminate and migrate to the posterior compartment, as well as cell death at the boundary (acridine orange staining). Expression under the control of Scer\GAL4GMR.PU also induces cell death, but not cell invasion, in the eye disc.
The expression of hepScer\UAS.cBa under the control of Scer\GAL4Bx-MS1096 does not lead to obvious size defects in third instar larval wing discs, as compared to controls.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4esg-NP5130 dramatically increases the number of mitotic cells in the adult gut.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4esg-NP5130 (using tub-gal80[ts] to limit the time of expression) increases cell proliferation in the adult gut.
Expression of hepScer\UAS.cBa driven by Scer\GAL4pnr-MD237 triggers cell death in the thorax and produces a small-scutellum phenotype.
Expression of hepScer\UAS.cBa along the anterior-posterior compartment boundary driven by Scer\GAL4ptc-559.1 induces elevated cell death in third instar wing discs relative to wild-type and results in the loss of the anterior crossvein.
The temporally regulated expression (by Gal80[ts]) of hepUAS.cBa, for 4 or 14 days under the control of Scer\GAL4NP5130, leads to strong increases in the proportion of mitotic cells and in the number of intestinal stem cells (assessed by immuno-staining for Delta) in the adult midgut, as compared to controls.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4twi.PG results in delayed or defective ventral furrow formation in a proportion of embryos.
Transient overexpression of hepScer\UAS.cBa in adults under the control of Scer\GAL4esg-NP5130 and Scer\GAL80ts.αTub84B induces increased proliferation of intestinal cells compared with controls.
Transient overexpression of hepScer\UAS.cBa in adults under the control of Scer\GAL4esg-NP5130 and Scer\GAL80ts.αTub84B results in significant lifespan shortening compared with wild-type.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4ptc-559.1 results in a dramatic increase in the number of intercalated cells and the formation of ectopic mixer cells at the segment boundaries during dorsal closure (in the abdominal segments of wild-type embryos at the end of dorsal closure, a mixer cell moves across the segment boundary from the anterior compartment to the posterior compartment and two cells from the ventral ectoderm intercalate into the leading edge, posterior to the mixer cell).
Ectopic expression of hepScer\UAS.cBa driven by Scer\GAL469B in embryos leads to cuticles with openings in the anterior part and puckering in the dorsal part.
Ectopic expression of hepScer\UAS.cBa driven by either Scer\GAL4Abd-B-LDN or Scer\GAL4ptc-559.1 leads to male genital disc effects such as incomplete rotation and separation of the plate from the abdomen.
Animals expressing hepScer\UAS.cBa under the control of Scer\GAL4ppl.PP show increased tolerance to paraquat compared to controls.
hepScer\UAS.cBa Scer\GAL4GMR.PF adults have normal eyes.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4GMR.PF does not affect eye development.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4GMR.PF has no effect on eye morphology.
Flies expressing hepScer\UAS.cBa, under the control of Scer\GAL4arm.PS, show a decreased sensitivity to paraquat compared to wild-type flies. This decreased sensitivity is also seen when hepScer\UAS.cBa is expressed under the control of the neuron-specific driver Scer\GAL4elav.Switch.PO, but only in the presence of RU486. However, expression of hepScer\UAS.cBa under the control of the muscle-specific driver Scer\GAL4Mhc.Switch.PO does not affect tolerance to paraquat. Overexpression of hepScer\UAS.cBa, driven by Scer\GAL4elav-C155, increases the lifespan of flies.
When expression is driven by Scer\GAL4hs.2sev, flies have rough eyes showing polarity phenotypes. Ommatidia are incorrectly rotated and sometimes exhibit the wrong chiral form.
Adults in which hepScer\UAS.cBa is expressed under the control of Scer\GAL4pnr-MD237 have a severely reduced scutellum, and there is a cleft in the tissue at the dorsal midline. The bristles are oriented in a different direction from normal, are loosely spaced and sometimes have kinks.
Scer\GAL4ptc.PU, hepUAS.cBa has abnormal cell migration | third instar larval stage phenotype, enhanceable by licUAS.ORF/Scer\GAL4ptc.PU
Scer\GAL4ptc.PU, hepUAS.cBa has abnormal cell migration | third instar larval stage phenotype, enhanceable by Hsap\MAP2K3UAS.cSa, Scer\GAL4ptc.PU
Scer\GAL4pnr-MD237, hepUAS.cBa has visible phenotype, enhanceable by pucE69
Scer\GAL4esg.PU, hepUAS.cBa has increased occurrence of cell division | adult stage phenotype, suppressible by Ets21CKK103211, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has increased occurrence of cell division | adult stage phenotype, suppressible by Ets21CRNAi.UAS.cMa, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has increased cell number | adult stage phenotype, suppressible by Ets21CKK103211, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has increased cell number | adult stage phenotype, suppressible by Ets21CRNAi.UAS.cMa, Scer\GAL4esg.PU
Scer\GAL4NP0001, hepUAS.cBa has increased occurrence of cell division | adult stage phenotype, suppressible by Ets21CKK103211, Scer\GAL4NP0001
Scer\GAL4NP0001, hepUAS.cBa has abnormal cell number | adult stage phenotype, suppressible by Ets21CKK103211, Scer\GAL4NP0001
Scer\GAL4NP5130, hepUAS.cBa has increased occurrence of cell division phenotype, suppressible by PEKGD5584, Scer\GAL4NP5130
Scer\GAL4pnr-MD237, hepUAS.cBa has abnormal size phenotype, suppressible | partially by wg[+]/wgl-8
Scer\GAL4pnr-MD237, hepUAS.cBa has visible phenotype, suppressible | partially by wg[+]/wgl-8
Scer\GAL4pnr-MD237, hepUAS.cBa has abnormal size phenotype, suppressible | partially by dsh3/dsh[+]
Scer\GAL4pnr-MD237, hepUAS.cBa has visible phenotype, suppressible | partially by dsh3/dsh[+]
Scer\GAL4pnr-MD237, hepUAS.cBa has abnormal size phenotype, suppressible | partially by arm2/arm[+]
Scer\GAL4pnr-MD237, hepUAS.cBa has visible phenotype, suppressible | partially by arm2/arm[+]
Scer\GAL4pnr-MD237, hepUAS.cBa has visible phenotype, suppressible by Scer\GAL4ptc-559.1/dshRNAi.UAS.cUa
Scer\GAL4ptc-559.1, hepUAS.cBa has increased cell death | third instar larval stage phenotype, suppressible by dsh3/dsh[+]
Scer\GAL4ptc-559.1, hepUAS.cBa has increased cell death | third instar larval stage phenotype, suppressible by Scer\GAL4ptc-559.1/dshRNAi.UAS.cUa
Scer\GAL4ptc.PU, hepUAS.cBa has abnormal cell migration | third instar larval stage phenotype, non-suppressible by licGD7546/Scer\GAL4ptc.PU
hepUAS.cBa, Scer\GAL4Bx-MS1096 is an enhancer of visible phenotype of DaxxEY09290, Scer\GAL4Bx-MS1096
hepUAS.cBa, Scer\GAL4Act5C.PI is an enhancer of neoplasia | somatic clone phenotype of Ras85DV12.UAS, Scer\GAL4Act5C.PI
hepUAS.cBa/Scer\GAL4Bx-MS1096 is an enhancer of visible phenotype of Scer\GAL4Bx-MS1096, byUAS.cLa
hepUAS.cBa, Scer\GAL4GMR.PF is an enhancer of visible phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
hepUAS.cBa/Scer\GAL4elav.PU is a suppressor of abnormal oxidative stress response phenotype of ben1
hepUAS.cBa/Scer\GAL4elav.PU is a suppressor of short lived phenotype of ben1
hepUAS.cBa/Scer\GAL4ey-OK107 is a suppressor of abnormal neuroanatomy | somatic clone phenotype of Mkk4e01485
hepUAS.cBa/Scer\GAL4ato.3.6 is a suppressor of abnormal neuroanatomy phenotype of dsh1
Scer\GAL4ptc.PU, hepUAS.cBa has anterior-posterior compartment boundary of the wing disc | third instar larval stage phenotype, enhanceable by licUAS.ORF/Scer\GAL4ptc.PU
Scer\GAL4ptc.PU, hepUAS.cBa has anterior-posterior compartment boundary of the wing disc | third instar larval stage phenotype, enhanceable by Hsap\MAP2K3UAS.cSa, Scer\GAL4ptc.PU
Scer\GAL4pnr-MD237, hepUAS.cBa has scutellum phenotype, enhanceable by pucE69
Scer\GAL4esg.PU, hepUAS.cBa has adult midgut epithelium phenotype, suppressible by Ets21CKK103211, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has adult midgut epithelium phenotype, suppressible by Ets21CRNAi.UAS.cMa, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has intestinal stem cell phenotype, suppressible by Ets21CKK103211, Scer\GAL4esg.PU
Scer\GAL4esg.PU, hepUAS.cBa has intestinal stem cell phenotype, suppressible by Ets21CRNAi.UAS.cMa, Scer\GAL4esg.PU
Scer\GAL4NP0001, hepUAS.cBa has adult midgut epithelium phenotype, suppressible | partially by Ets21CKK103211, Scer\GAL4NP0001
Scer\GAL4NP0001, hepUAS.cBa has intestinal stem cell phenotype, suppressible by Ets21CKK103211, Scer\GAL4NP0001
Scer\GAL4NP0001, hepUAS.cBa has adult midgut enterocyte phenotype, suppressible by Ets21CKK103211, Scer\GAL4NP0001
Scer\GAL4NP5130, hepUAS.cBa has adult gut phenotype, suppressible by PEKGD5584, Scer\GAL4NP5130
Scer\GAL4ptc-559.1, hepUAS.cBa has anterior crossvein phenotype, suppressible by Scer\GAL4ptc-559.1/dshRNAi.UAS.cUa
Scer\GAL4pnr-MD237, hepUAS.cBa has scutellum phenotype, suppressible | partially by wg[+]/wgl-8
Scer\GAL4pnr-MD237, hepUAS.cBa has scutellum phenotype, suppressible | partially by dsh3/dsh[+]
Scer\GAL4pnr-MD237, hepUAS.cBa has scutellum phenotype, suppressible | partially by arm2/arm[+]
Scer\GAL4ptc-559.1, hepUAS.cBa has anterior crossvein phenotype, suppressible | partially by dsh3/dsh[+]
Scer\GAL4NP5130, hepUAS.cBa has midgut | adult stage phenotype, suppressible by Xbp1UAS.RB/Scer\GAL4NP5130
Scer\GAL4twi.PG, hepUAS.cBa has ventral furrow phenotype, suppressible | germline clone by bskunspecified
Scer\GAL4ptc.PU, hepUAS.cBa has anterior-posterior compartment boundary of the wing disc | third instar larval stage phenotype, non-suppressible by licGD7546/Scer\GAL4ptc.PU
hepUAS.cBa, Scer\GAL4Bx-MS1096 is an enhancer of wing phenotype of DaxxEY09290, Scer\GAL4Bx-MS1096
hepUAS.cBa/Scer\GAL4GMR.PF is an enhancer of eye phenotype of Scer\GAL4GMR.PF, foxoUAS.cPa
hepUAS.cBa/Scer\GAL4Bx-MS1096 is an enhancer of wing phenotype of Scer\GAL4Bx-MS1096, byUAS.cLa
hepUAS.cBa, Scer\GAL4GMR.PF is an enhancer of eye phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
hepUAS.cBa, Scer\GAL4GMR.PF is an enhancer of ommatidium phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
hepUAS.cBa/Scer\GAL4ey-OK107 is a suppressor of Kenyon cell | somatic clone phenotype of Mkk4e01485
hepUAS.cBa/Scer\GAL4ey-OK107 is a suppressor of axon | somatic clone phenotype of Mkk4e01485
hepUAS.cBa/Scer\GAL4ato.3.6 is a suppressor of axon & dorsal cluster neuron phenotype of dsh1
hepUAS.cBa/Scer\GAL4VP16.arm is a suppressor of embryonic epidermis | dorsal phenotype of arm3
hepUAS.cBa/Scer\GAL4VP16.arm is a suppressor of embryonic epidermis | ventral phenotype of arm3
Scer\GAL4Bx-MS1096, aPKCUAS.Tag:CAAX(Unk), hepUAS.cBa has wing disc | third instar larval stage phenotype
Ras85DV12.UAS, Scer\GAL4Act5C.PI, hepUAS.cBa has larval brain | somatic clone phenotype
The co-expression of hepScer\UAS.cBa and aPKCCAAXWT.Scer\UAS under the control of Scer\GAL4Bx-MS1096 leads to moderate overgrowth and cell polarity defects in third instar larval wing discs, as compared to controls.
The increased cell proliferation observed upon expression of hepScer\UAS.cBa under the control of Scer\GAL4esg-NP5130 in the adult gut is suppressed by co-expression of either Sox21aJF02191 or kaydsRNA.Scer\UAS.
The increased cell proliferation in the adult gut expressing hepScer\UAS.cBa under the control of Scer\GAL4esg-NP5130 (using tub-gal80[ts] to limit the time of expression) is suppressed by co-expression of PEKGD5584.
Expression of hepScer\UAS.cBa under the control of Scer\GAL4elav.PU fully rescues the reduced oxidative stress resistance and shortened lifespan seen in ben1 mutant males.
The reduced wing phenotype caused by expression of DLPEY09290 under the control of Scer\GAL4Bx-MS1096 is strongly exacerbated by co-expression of hepScer\UAS.cBa.
The defects in ventral furrow formation seen in embryos expressing hepScer\UAS.cBa under the control of Scer\GAL4twi.PG are completely suppressed in embryos derived from bskunspecified female germline clones.
The axon overextension phenotype of Mkk4e01485 neuroblast clones in mushroom bodies is suppressed by expression of hepScer\UAS.cBa using Scer\GAL4ey-OK107.
The increased tolerance of animals expressing hepScer\UAS.cBa under the control of Scer\GAL4ppl.PP to paraquat is abolished by NLazNW5/NLazNW5, with the double mutant flies showing the same sensitivity to paraquat as NLazNW5/NLazNW5 single mutants.
Expression of hepScer\UAS.cBa, under the control of Scer\GAL4ato.3.6, in a dsh1 background results in a large increase of dorsal cluster neuron axons crossing the optic chiasm, indicating a complete dominance of the hep gain of function phenotype.
Coexpression of hepScer\UAS.cBa and Ras85DV12.Scer\UAS under the control of Scer\GAL4Act5C.PI results in eye/antennal imaginal disc clones results in the invasion of the disc cells into the ventral nerve cord and regions of the brain.
The small, deformed eye phenotype of foxoScer\UAS.cPa; Scer\GAL4GMR.PF adults is enhanced by the presence of hepScer\UAS.cBa.
When hepScer\UAS.cBa is coexpressed with one copy of Traf1EP578, driven by Scer\GAL4GMR.PF, the number of ommatidia and the size of the compound eye are reduced to similar levels seen when two copies of Traf1EP578 are expressed.
Coexpression of Traf2EP1516 with either hepScer\UAS.cBa, under the control of Scer\GAL4GMR.PF, does not affect the development of eyes.
The phenotype caused when hepScer\UAS.cBa is expressed under the control of Scer\GAL4pnr-MD237is enhanced by a single copy of pucE69; the scutellum is completely missing.
The rough eye phenotype caused by expression of Hsap\MAPTV337M.Scer\UAS under the control of Scer\GAL4GMR.PF is enhanced by co-expression of hepScer\UAS.cBa; eye surface roughness is increased, eye size is decreased and necrotic black patches are formed in the eye.
Expression of hepScer\UAS.cBa with Scer\GAL4ey-OK107 rescues the axonal phenotypes seen in hepr39 mushroom body clones.