P{PZ} insertion 492bp upstream of the AUG start codon of the 1A cDNA.
98% of hemisegments show ISNb guidance defects in homozygous embryos. The ISNb axons often fail to defasciculate from one another, resulting in an abnormally thick morphology and a failure to reach their muscle targets. In addition, ISNb axons that follow aberrant pathways and fasciculate ectopically with adjacent axons (including the transverse nerve) are seen.
90% of hemisegments show defects in the SNa axon in homozygous embryos. The dorsal or lateral SNa branches are often missing.
ISN axons fail to target the correct muscles in homozygous embryos. The first or second branches often extend dorsally beyond their correct muscle fields. Occasionally mutant ISN axons cross the segment boundary and fasciculate with adjacent ISN axons.
pbl[+]/pbl09645 is a non-enhancer of abnormal eye color phenotype of Hsap\MECP2R294X.UAS, Scer\GAL4GMR.PU
pbl[+]/pbl09645 is a non-suppressor of abnormal eye color phenotype of Hsap\MECP2R294X.UAS, Scer\GAL4GMR.PU
pbl[+]/pbl09645 is a non-enhancer of eye phenotype of Hsap\MECP2Δ166.UAS, Scer\GAL4GMR.PU
pbl[+]/pbl09645 is a suppressor of eye phenotype of Hsap\MECP2UAS.FL, Scer\GAL4GMR.PU
pbl[+]/pbl09645 is a non-suppressor of eye phenotype of Hsap\MECP2Δ166.UAS, Scer\GAL4GMR.PU
pbl09645 is partially rescued by Scer\GAL4sca-537.4/pblUAS.N.Tag:HA
pbl09645 is not rescued by Scer\GAL4how-24B/pblUAS.N.Tag:HA
Expression of pblScer\UAS.N.T:Ivir\HA1 under the control of Scer\GAL4how-24B fails to rescue the motor axon pathfinding defects seen in pbl09645 embryos.
Expression of pblScer\UAS.N.T:Ivir\HA1 under the control of Scer\GAL4sca-537.4 partially but significantly rescues the pathfinding defects in the ISNb and SNa, but not the ISN, motor axon pathways in pbl09645 embryos.
A. Spradling.
Excision of the P{lacW} is accompanied by a reversion to wild-type.
Complements: l(3)0721707217. Complements: l(3)neo121.