UAS regulatory sequences drive expression of a short inverted repeat.
Expression of Dscam1HMS01859 under the control of Scer\GAL4eve.RN2 results in defects in dendritogenesis in the embryonic aCC motoneurons (decreased number of dendritic tips, misplacement of primary branches) compared to controls. Loss of dendritic tips at the aCC neuron is also observed when the RNAi is driven with Scer\GAL4elav.PU in combination with Scer\GAL80eve.RN2 (thus excluding the expression from the aCC cells) or any of these drivers: Scer\GAL4[GMR23E04], Scer\GAL4c544, Scer\GAL4GMR37G09 or Scer\GAL4ftz.ng but not when any of the following drivers are used: Scer\GAL4GMR30C11, Scer\GAL4GMR13G08, Scer\GAL4GMR31E09, Scer\GAL4GMR65G01, Scer\GAL4GMR37G07, Scer\GAL4GMR19H09, Scer\GAL4GMR53D04, Scer\GAL4GMR24B02, Scer\GAL4sli.PS, Scer\GAL4GMR34B10, Scer\GAL4GMR30E02, Scer\GAL4GMR32D08, Scer\GAL4GMR55H07, Scer\GAL4GMR22B04, Scer\GAL4GMR11B11, Scer\GAL4GMR27G12 and Scer\GAL4GMR64F12. Both Scer\GAL4GMR23E04 and Scer\GAL4c544 drive expression in a random half of all MP1 neurons (but not in aCCs) and dendritogenesis defects are seen in aCC cells that run across an MP1 axon expressing the Dscam1HMS01859 RNAi, no defects in the positioning of either the MP1 or the aCC neurons are observed in these embryos.
Dscam1HMS01859, Scer\GAL4eve.RN2 has abnormal neuroanatomy | embryonic stage phenotype, suppressible | partially by PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has abnormal neuroanatomy | embryonic stage phenotype, non-suppressible by PakUAS.mEos2, Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has abnormal neuroanatomy | embryonic stage phenotype, non-suppressible by Cdc424/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has abnormal neuroanatomy | embryonic stage phenotype, non-suppressible by Cdc426/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has larval DA1 motor neuron | embryonic stage phenotype, suppressible | partially by PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has dendrite | embryonic stage phenotype, suppressible | partially by PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has larval DA1 motor neuron | embryonic stage phenotype, non-suppressible by PakUAS.mEos2, Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has dendrite | embryonic stage phenotype, non-suppressible by PakUAS.mEos2, Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has larval DA1 motor neuron | embryonic stage phenotype, non-suppressible by Cdc424/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has dendrite | embryonic stage phenotype, non-suppressible by Cdc424/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has larval DA1 motor neuron | embryonic stage phenotype, non-suppressible by Cdc426/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
Dscam1HMS01859, Scer\GAL4eve.RN2 has dendrite | embryonic stage phenotype, non-suppressible by Cdc426/PakUAS.Tag:Myr(Src64B), Scer\GAL4eve.RN2
The dendritogenesis defects in the embryonic aCC motoneurons characteristic for embryos expressing Dscam1HMS01859 RNAi under the control of Scer\GAL4eve.RN2 are partially suppressed by co-expression of PakScer\UAS.T:Myr-Src64B : the reduced dendritic number is fully restored but the region containing primary dendritic processes is expanded compared to controls. This rescue effect is however blocked in the presence of either Cdc426 or Cdc424 (in hemizygous state). No suppression of the loss of dendritic tips is observed upon co-expression with PakScer\UAS.T:Lhem\EosFP-m2.