PuZ22 adult heterozygous males show significant decrease in locomotion activity compared to wild-type controls.
Homozygous embryos have a disrupted tracheal network, with misdirected tubules and ectopic branching in addition to disruption of the dorsal trunk.
67% of heterozygous embryos show ectopic tracheal migration.
Cuticle defects.
Pu[+]/PuZ22 is an enhancer of partially lethal - majority die phenotype of TorsinKO13
Pu[+]/PuZ22, TorsinKO13 has abnormal locomotor behavior | third instar larval stage phenotype
PuZ22 has embryonic/larval tracheal system phenotype, enhanceable by awdj2A4/awd[+]
PuZ22 has embryonic/larval tracheal system phenotype, enhanceable by shi2
PuZ22 has embryonic/larval tracheal system phenotype, suppressible | partially by btlH82Δ3/btl[+]
PuZ22 has embryonic/larval tracheal system phenotype, suppressible | partially by Catsup[+]/Catsup26
Pu[+]/PuZ22 is an enhancer of embryonic/larval tracheal system phenotype of awdj2A4
Pu[+]/PuZ22 is an enhancer of embryonic/larval tracheal system phenotype of shi2
Pu[+]/PuZ22 is a suppressor of embryonic/larval tracheal system phenotype of Catsup26
Pu[+]/PuZ22 is a suppressor of embryonic/larval tracheal system phenotype of btlH82Δ3
Double heterozygous TorsinKO13/+; PuZ22/+ female larvae show very significantly reduced peristaltic frequency relative to either single heterozygote.
While TorsinKO13/Y third instar larvae are mostly viable, very few TorsinKO13/Y ; PuZ22/+ third instar larvae are observed.
The penetrance and severity of the ectopic tracheal migration phenotype is increased in PuZ22/+ awdj2A4 double mutant embryos compared to either single mutant.
The penetrance and severity of the ectopic tracheal migration phenotype is increased in PuZ22/+ shi2 double mutant embryos compared to either single mutant.
The opposing tracheal phenotypes of PuZ22/+ and btlH82Δ3/+ single heterozygous embryos (ectopic migration and lack of migration respectively) are both partially suppressed in PuZ22/+ btlH82Δ3/+ double heterozygous embryos.
The ectopic tracheal migration phenotype of PuZ22/+ single heterozygous embryos is partially suppressed and the lack of tracheal migration phenotype of Catsup26/+ single heterozygous embryos is completely suppressed in PuZ22/+ Catsup26/+ double heterozygous embryos.
PuZ22 is partially rescued by PuUAS.cHa/Scer\GAL4btl.PS
Expression of PuScer\UAS.cHa under the control of Scer\GAL4btl.PS can rescue the ectopic tracheal branch migration see in PuZ22 embryos.
Class II Pu allele.