Expression of one copy of jingScer\UAS.cSa under the control of Scer\GAL4GMR.PF has no visible effects on ommatidial formation.
Expression of jingScer\UAS.cSa under the control of Scer\GAL4elav.PLu results in thinner longitudinal connectives than normal and reduced spacing between the anterior and posterior commissures.
Expression of jingScer\UAS.cSa under the control of Scer\GAL4sli.PS results in an increase in the number of midline glial cells compared to wild type, with an average of 12 glia per segment that are scattered laterally from the midline compared to 8 in wild-type embryos. The extra glia are still located dorsally to the ventral nerve cord. There is no cell death present in the glial population in these embryos, in contrast to the small apoptotic glia found surrounding the nerve cord in wild-type embryos. Commissural axons do not properly approach the midline in embryos expressing jingScer\UAS.cSa under the control of Scer\GAL4sli.PS and instead appear stalled along the longitudinal tracts. The extra glia present in these embryos appear to migrate towards the longitudinal tracts. Expression of jingScer\UAS.cSa under the control of Scer\GAL4GMR.PF results in flies with a rough eye phenotype, consisting of highly disorganised ommatidia and mechanosensory bristles in 45% of flies. In addition the number of ommatidia is reduced by 50% compared to wild type.
Expression of jingScer\UAS.cSa under the control of Scer\GAL4sim.P3.7 inhibits the formation of the preoral and postoral tritocerebral commissures in the embryonic brain. The circumesophageal longitudinal connectives sometimes do not extend properly and have large gaps.
When jingScer\UAS.cSa is driven by Scer\GAL4sim.P3.7, commissural and longitudinal axon formation is inhibited. When jingScer\UAS.cSa is driven by Scer\GAL4btl.PS, defects are seen in dorsal trunk fusion, as well as improper formation of the transverse connective, dorsal branch and visceral branch.
Scer\GAL4elav.PLu, jingUAS.cSa has abnormal neuroanatomy phenotype, enhanceable by XNPEP635/Scer\GAL4elav.PLu
Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype, suppressible by Df(2L)TW50/+
Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype, suppressible by Df(2R)Egfr5/+
Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype, suppressible by spi1/spi[+]
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of visible phenotype of Scer\GAL4GMR.PF, kayEP3084
jingUAS.cSa/Scer\GAL4elav.PLu is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4elav.PLu, XNPEP635
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of visible phenotype of Scer\GAL4GMR.PF, lapEP3060
jingUAS.cSa, Scer\GAL4GMR.PF is a non-enhancer of visible phenotype of EgfrElp.UAS, Scer\GAL4GMR.PF
BicDREP3705, Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype
Scer\GAL4GMR.PF, jigr1EP3354, jingUAS.cSa has visible phenotype
D1EP473, Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype
Scer\GAL4GMR.PF, XNPEP635, jingUAS.cSa has visible phenotype
Atx2EP3145, Scer\GAL4GMR.PF, jingUAS.cSa has visible phenotype
Scer\GAL4elav.PLu, jingUAS.cSa has larval longitudinal connective phenotype, enhanceable by XNPEP635/Scer\GAL4elav.PLu
jingUAS.cSa has ommatidium phenotype, suppressible by Df(2R)Egfr5/+
jingUAS.cSa has ommatidium phenotype, suppressible by spi1/spi[+]
Scer\GAL4sli.PS, jingUAS.cSa has larval ventral midline glial cell | ectopic phenotype, suppressible by SIIN/SIIN
Scer\GAL4sli.PS, jingUAS.cSa has larval ventral midline glial cell | ectopic phenotype, suppressible by spi1/spi1
jingUAS.cSa has ommatidium phenotype, suppressible by Df(2L)TW50/+
Scer\GAL4sli.PS, jingUAS.cSa has larval ventral midline glial cell | ectopic phenotype, non-suppressible by S[+]/SIIN
Scer\GAL4sli.PS, jingUAS.cSa has larval ventral midline glial cell | ectopic phenotype, non-suppressible by spi1/spi[+]
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of eye phenotype of Scer\GAL4GMR.PF, kayEP3084
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of ommatidium phenotype of Scer\GAL4GMR.PF, kayEP3084
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of pigment cell phenotype of Scer\GAL4GMR.PF, kayEP3084
jingUAS.cSa/Scer\GAL4elav.PLu is an enhancer of larval longitudinal connective phenotype of Scer\GAL4elav.PLu, XNPEP635
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of eye phenotype of Scer\GAL4GMR.PF, lapEP3060
jingUAS.cSa/Scer\GAL4GMR.PF is an enhancer of ommatidium phenotype of Scer\GAL4GMR.PF, lapEP3060
jingUAS.cSa, Scer\GAL4GMR.PF is a non-enhancer of eye phenotype of EgfrElp.UAS, Scer\GAL4GMR.PF
jingUAS.cSa, Scer\GAL4GMR.PF is a non-enhancer of ommatidium phenotype of EgfrElp.UAS, Scer\GAL4GMR.PF
jingUAS.cSa/Scer\GAL4sli.PS is a non-suppressor of larval ventral midline glial cell phenotype of SIIN
jingUAS.cSa/Scer\GAL4sli.PS is a non-suppressor of larval ventral midline glial cell phenotype of spi1
D1EP473, Scer\GAL4GMR.PF, jingUAS.cSa has eye phenotype
D1EP473, Scer\GAL4GMR.PF, jingUAS.cSa has ommatidium phenotype
BicDREP3705, Scer\GAL4GMR.PF, jingUAS.cSa has eye phenotype
BicDREP3705, Scer\GAL4GMR.PF, jingUAS.cSa has ommatidium phenotype
Scer\GAL4GMR.PF, jigr1EP3354, jingUAS.cSa has eye phenotype
Scer\GAL4GMR.PF, jigr1EP3354, jingUAS.cSa has ommatidium phenotype
Scer\GAL4GMR.PF, XNPEP635, jingUAS.cSa has eye phenotype
Scer\GAL4GMR.PF, XNPEP635, jingUAS.cSa has ommatidium phenotype
Atx2EP3145, Scer\GAL4GMR.PF, jingUAS.cSa has eye phenotype
Atx2EP3145, Scer\GAL4GMR.PF, jingUAS.cSa has ommatidium phenotype
Scer\GAL4GMR.PF, jingUAS.cSa, lapEP3060 has pigment cell phenotype
Co-expression of jingScer\UAS.cSa enhances the severity of the rough eye phenotype caused by expression of lapEP3060 under the control of Scer\GAL4GMR.PF and in addition, loss of pigmentation in the eye is seen.
Co-expression of jingScer\UAS.cSa and XNPEP635 under the control of Scer\GAL4elav.PLu results in synergistic effects in the embryonic central nervous system; 65% of segments have no longitudinal connectives.
The increase in the number of midline glia per ventral nerve cord segment seen in embryos expressing jingScer\UAS.cSa under the control of Scer\GAL4sli.PS is not suppressed by spi1, but expression of jingScer\UAS.cSa under the control of Scer\GAL4sli.PS in a homozygous spi1 background does not induce extra midline glia and the number of midline glia per ventral nerve cord segment in these double mutant embryos is reduced compared to wild type and is similar to that seen in homozygous spi1 single mutants. The rough eye phenotype caused by expression of EgfrElp.Scer\UAS under the control of Scer\GAL4GMR.PF is not enhanced by coexpression of jingScer\UAS.cSa. The rough eye phenotype caused by expression of jingScer\UAS.cSa under the control of Scer\GAL4GMR.PF is dominantly suppressed by spi1, Df(2L)TW50 or Df(2R)Egfr5.