photoreceptor cell | precursor & nucleus, with Scer\GAL4unspecified
photoreceptor cell | precursor & nucleus, with Scer\GAL4unspecified, msn03349
Expression of msnDN.Scer\UAS under the control of Scer\GAL4twi.PG results in delayed or defective ventral furrow formation in a proportion of embryos.
Expression of msnDN.Scer\UAS in the whole epidermis of embryos, driven by Scer\GAL4e22c, results in breaks in the localization of actin and myosin at the epithelial margin. These gaps correlate with reduced elongation and leading edge constriction of the affected cells. The same phenotype is seen when msnDN.Scer\UAS is expressed in the marginal cells of the epidermis using Scer\GAL4LE.
Expression of msnDN.Scer\UAS in the amnioserosa cells of embryos, driven by Scer\GAL4c381, results in head problems in less than 10% of embryos, which vary from an anterior hole to dorsal-anterior holes.
When msnDN.Scer\UAS is expressed in the developing eye of msn03349/+ animals a R-cell nuclear migration phenotype is seen in 47% of mutant eye discs. Only 5% of msn03349/+ eye discs show this phenotype on its own.
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, enhanceable by Df(2L)TW119
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, enhanceable by Lis-1k13209
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, enhanceable by BicDr5
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, non-enhanceable by Cdc423
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, non-enhanceable by Pak6
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, non-enhanceable by bsk2
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, non-enhanceable by capuM732
Scer\GAL4unspecified, msnDN.UAS has photoreceptor cell | precursor & nucleus phenotype, non-enhanceable by klarmarb-BX5
Scer\GAL4twi.PG, msnDN.UAS has ventral furrow phenotype, non-suppressible | germline clone by bskunspecified
The defects in ventral furrow formation seen in embryos expressing msnDN.Scer\UAS under the control of Scer\GAL4twi.PG are not suppressed in embryos derived from bskunspecified female germline clones.
42% of animals expressing msnDN.Scer\UAS in the developing eye, combined with BicDr5/+ exhibit a R-cell nuclear migration phenotype. 37% of animals expressing msnDN.Scer\UAS in the developing eye, combined with Df(2L)TW119/+ exhibit a R-cell nuclear migration phenotype. 7% of animals expressing msnDN.Scer\UAS in the developing eye, combined with bsk2/+ exhibit a R-cell nuclear migration phenotype. 0% of animals expressing msnDN.Scer\UAS in the developing eye, combined with capuM732/+ exhibit a R-cell nuclear migration phenotype. 0% of animals expressing msnDN.Scer\UAS in the developing eye, combined with Cdc423/+ exhibit a R-cell nuclear migration phenotype. 21% of animals expressing msnDN.Scer\UAS in the developing eye, combined with Lis-1k13209/+ exhibit a R-cell nuclear migration phenotype. 0% of animals expressing msnDN.Scer\UAS in the developing eye, combined with klarmarb-BX5/+ exhibit a R-cell nuclear migration phenotype. 0% of animals expressing msnDN.Scer\UAS in the developing eye, combined with Pak6/+ exhibit a R-cell nuclear migration phenotype.
Scer\GAL4unspecified/msnDN.UAS fails to rescue msn03349/msn[+]