LanB1GD13179, Scer\GAL4tj.PU, mysdin.UAS has egg chamber phenotype
Scer\GAL4Mef2.PR, ifUAS.cMBa, mysdin.UAS has larval somatic muscle cell phenotype
Scer\GAL4how-24B, ifUAS.cMBa, mysdin.UAS has muscle cell phenotype
Overexpression of ifScer\UAS.cMBa and mysdin.Scer\UAS in the somatic muscle under the control of Scer\GAL4Mef2.PR leads to pointed morphology of the muscle ends and subsequent torn muscles.
Expression of mysdin.Scer\UAS and ifScer\UAS.cMBa under the control of Scer\GAL4how-24B results in a muscle-detachment phenotype.
mysdin.UAS/Scer\GAL448Y partially rescues mys11
Scer\GAL4twi.PG, Scer\GAL4how-24B, mysdin.UAS partially rescues mys11
The addition of mysdin.Scer\UAS driven by Scer\GAL4Kr.PM rescues the germ band retraction defects seen embryos that are mys11 for both in maternal and zygotic mys.
Rescues the ability of the endodermal midgut cells of embryos that lack maternal and zygotic mys function (derived from homozygous mys11 female germline clones) to send projections and to migrate, although there is a small delay in migration, when expressed under the control of Scer\GAL448Y. The visceral mesoderm and germband retraction defects are not rescued in these embryos. mysdin.Scer\UAS expressed under the control of both Scer\GAL4twi.PG and Scer\GAL4how-24B rescues the visceral mesoderm defects of embryos that lack maternal and zygotic mys function (derived from homozygous mys11 female germline clones) but does not rescue the migration defects of the endodermal midgut cells in these embryos.