P{PZ} insertion in the first intron.
fry1/fry02240 mutant third instar larvae show a significant increase in the proportion of dorsal midline ddaC dendritic length that is enclosed within the epidermis rather than attached to the ECM. Dendrite crossing is seen in these mutants, and the majority of these crossings are between enclosed dendrites and dendrites attached to the ECM and are thus non-contacting. Unlike in wild type, crossing is also seen between dendrites on the interface between the v'ada and the vdaB neurons. These crossings are non-contacting.
Homozygotes often die as pharate adults. Cells in the wing of pharate adults form a cluster of hairs. The multiple wing hair phenotype is also seen in pupae late in hair development (more than 36 hours after the white pupa stage), while at earlier times the phenotype seems weaker. One or a few branched bristles are seen in the abdomen, legs, notum and triple row of homozygous pharate adults. These bristles are relatively normal in shape and length except for the branching. In some cases, several branches are seen at the same proximal/distal location along the shaft. Bristles with extensive splitting are occasionally seen and these are often shorter than normal. On the head, some bristles are bent, distorted and shorter than normal without being excessively split. The phenotype of developing bristles in the pupa (assayed by staining the actin cytoskeleton) overlaps that of the adult bristle phenotype. Homozygous or hemizygous pharate adults show extensive branching of essentially all arista laterals and they are thinner than normal and appear curled distally. Equivalent defects are seen in developing arista laterals in pupae.
fry02240/fry1 has abnormal neuroanatomy | third instar larval stage phenotype, suppressible by mewUAS.cMBa/mysUAS.cDa/Scer\GAL4ppk.PH
fry02240 is a suppressor of visible phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
fry02240, stan[+]/stanE59 has abnormal neuroanatomy | third instar larval stage phenotype
fry02240/fry1 has larval dorsal multidendritic neuron ddaC | third instar larval stage phenotype, suppressible by mewUAS.cMBa/mysUAS.cDa/Scer\GAL4ppk.PH
fry02240 is a suppressor of eye phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
fry02240 is a suppressor of ommatidium phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
fry02240, stan[+]/stanE59 has dendrite | third instar larval stage phenotype
fry02240, stan[+]/stanE59 has larval dorsal multidendritic neuron ddaC | third instar larval stage phenotype
Co-expression of mysScer\UAS.cDa and mewScer\UAS.cMBa the control of Scer\GAL4ppk.PH rescues the increase in epidermally enclosed dendrites seen in fry1/fry02240 mutants. The dendritic crossing seen in fry1/fry02240 mutants is also largely rescued. The dendritic crossings that remain in the rescue flies are between two ECM attached dendrites, rather than non-contacting crossings between an epidermally enclosed dendrite and one attached to the ECM. The crossing on the v'ada/vdaB interface is also mostly rescued and all non-contacting crossing is eliminated.
The rough eye phenotype caused by expression of Hsap\MAPTV337M.Scer\UAS under the control of Scer\GAL4GMR.PF is suppressed by fry02240.
A. Spradling.
Excision of the P{PZ} element can revert the mutant phenotype.
Complements: simj01814. Complements: cpo01824. Complements: l(3)0185901859. Complements: l(3)rK145rK145.