Amino acid replacement: T559D. The primer used to introduce the point mutation (CGTGACAAGTACAAagatctCCGCGAGATTCGTAAGGG) also silently introduced a BglII site (lower case in primer sequence).
rhabdomere & cytoskeleton | apical, with Scer\GAL4hs.PB
rhabdomere & microvillus, with Scer\GAL4hs.PB
rhabdomere & plasma membrane | apical, with Scer\GAL4hs.PB
Tracheal terminal cells expressing the phosphomimetic isoform MoeK.T559D.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4bs.PM exhibit abnormal dilations of the lumenal membrane and reduced branch number.
The lamina plexus is uneven and irregular, thick axons bundles are seen in the medulla in third instar larvae expressing MoeK.T559D.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4sca-109-68.
When MoeK.T559A.Scer\UAS.T:Hsap\MYC; Scer\GAL4hs.PB pupae are heat shocked during apical morphogenesis of the rhabdomeres, microvilli at the apical surface of rhabdomeres become irregular: the apical membrane between adherens junctions is severely disorganized in these cells, as is the apical cytoskeleton.
MoeK.T559D.UAS.Tag:MYC/Scer\GAL4332.3 is a suppressor | partially of majority die during embryonic stage phenotype of crbGX24w-/crb11A22, crbY10A
MoeK.T559D.UAS.Tag:MYC/Scer\GAL4332.3 is a suppressor | partially of embryo | dorsal closure stage phenotype of crbGX24w-/crb11A22, crbY10A
MoeK.T559D.UAS.Tag:MYC/Scer\GAL4332.3 is a suppressor | partially of embryonic/first instar larval cuticle | embryonic stage phenotype of crbGX24w-/crb11A22, crbY10A
Expression of MoeK.T559D.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4332.3 partially suppresses the embryonic lethality and dorsal closure defects seen in embryos expressing crbY10A in a crbGX24w-/crb11A22 background.