macrochaeta & adult abdomen | somatic clone | cell non-autonomous
microchaeta & adult abdomen | somatic clone | cell non-autonomous
microchaeta & adult thorax | somatic clone | cell non-autonomous
wing & macrochaeta
Mutant embryos show salivary gland guidance defects; a large portion of the salivary gland curves towards the central nervous system, instead of lying parallel to the midline as in wild-type embryos.
When mutant clones are made in the developing eye, no R-cell precursor nuclear migration phenotype was seen.
Bristles and hairs on the adult abdomen and thorax show altered polarity. Clones reveal the effect shows domineering non-autonomy. fz1 phenotypes differ from in1 and fy1 in two ways. In fz1 the hairs on the scutellum show a complicated pattern rather than pointing anteriorly, and thorax microchaetae are not routinely split. On the leg, femoral bracts are mispositioned indicating abnormal polarity. Tarsal segments may have parts missing and/or duplicated and show cuticular blebs. Eyes show a rough eye phenotype due to ommatidial disorganisation. Pupal wings show miseversion phenotype - many pupae show an everting wing oriented anteriorly and sometimes dorsally.
Embryos lacking maternal and zygotic fz function (derived from a cross between fz1/fz30 males and females) are missing the RP2/sib lineage in 1-2 hemisegments in 10% of cases. Embryos lacking maternal and zygotic fz function (derived from a cross between fz1/fz23 males and females) are missing the RP2/sib lineage in 1-2 hemisegments in 11% of cases.
Homozygous embryos derived from homozygous females have a negligible segment-polarity phenotype. Injection of dsRNA produced by annealing fz2L.cKa and fz2a.L.cKa RNA into these embryos results in segment polarity phenotypes.
Bristle polarity phenotype.
moderate thoracic bristle phenotype moderate wing-hair disorientation
fz1/fz1 is a non-enhancer of visible | adult stage phenotype of in1
fz1/fz1 is a non-enhancer of abnormal planar polarity | adult stage phenotype of in1
fz1/fz1 is a non-enhancer of visible | adult stage phenotype of frtz30
fz1/fz1 is a non-enhancer of abnormal planar polarity | adult stage phenotype of frtz30
fz1/fz1 is a non-enhancer of visible | adult stage phenotype of fy2
fz1/fz1 is a non-enhancer of abnormal planar polarity | adult stage phenotype of fy2
fz1 is a non-enhancer of abnormal neuroanatomy | embryonic stage phenotype of mud3
fz1 is a non-enhancer of visible phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
fz[+]/fz1 is a suppressor | partially of decreased size | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
fz[+]/fz1 is a suppressor | partially of visible | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
fz1 is a non-suppressor of visible phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
fz1 has presumptive embryonic salivary gland phenotype, enhanceable by drlR343
fz1 has tarsal segment phenotype, non-enhanceable by fy1
fz1 has tarsal segment phenotype, non-enhanceable by in1
fz1 has ommatidium phenotype, non-suppressible by fy1
fz1 has ommatidium phenotype, non-suppressible by in1
fz1 has tarsal segment phenotype, non-suppressible by fy1
fz1 has tarsal segment phenotype, non-suppressible by in1
fz1 is an enhancer of presumptive embryonic salivary gland phenotype of drlR343
fz1/fz1 is a non-enhancer of abdominal sternite bristle phenotype of in1
fz1/fz1 is a non-enhancer of abdominal sternite bristle phenotype of frtz30
fz1/fz1 is a non-enhancer of abdominal sternite bristle phenotype of fy2
fz1 is a non-enhancer of larval ventral nerve cord | embryonic stage phenotype of mud3
fz1 is a non-enhancer of larval ventral nerve cord commissure | embryonic stage phenotype of mud3
fz1 is a non-enhancer of eye phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
fz[+]/fz1 is a suppressor | partially of eye phenotype of Nab2EP3716, Scer\GAL4GMR.PU
fz1 is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
fz1 is a non-suppressor of ommatidium phenotype of Rac1V12.hs.sev
Df(1)NetABΔ, fz1 has larval ventral nerve cord | embryonic stage phenotype
Df(1)NetABΔ, fz1 has larval ventral nerve cord commissure | embryonic stage phenotype
Df(3L)N2-27, fz1 has larval RP2 motor neuron phenotype
Scer\GAL4hs.2sev, dshUAS.cNa, fz1 has ommatidium phenotype
fy2;fz1 double mutant adults display hair polarity defects in abdominal bristles that are similarly severe as in fy2 single mutants and the severity of abdominal bristle polarity phenotype in1,fz1 double mutant is similar to in single mutants. The frtz30;fz1 double mutant have abdominal bristle defects that are comparable to frtz30 single mutants.
fz1, Df(1)NetABΔ double mutant embryos display a severe lack of commissures in the ventral nerve cord.
fz1, mud3 mutant embryos do not display any more severe ventral nerve cord phenotypes, as compared to each single mutant.
ParpGMR.PU shows no genetic interaction with fz1/+.
All fz1/fz1; Df(3L)N2-27 double mutant embryos show RP2/sib lineage defects, with 6-11 hemisegments per embryo being affected.
Scer\GAL4hs.2sev/fz1 partially rescues fzUAS.cAa
fz1 somatic clones in the eye in a fzsevE3.SevP.PS background: In the center of clones, 15%-25% of ommatidia showed dorso-ventral inversions, as observed in eyes wholly mutant for fz in a fzsevE3.SevP.PS background. However, on the polar edge of the clone, 40%-60% of ommatidia are inverted, whereas, on the equatorial edge, only 5% are inverted. These inversions are also seen on outside the clone, near its polar boundary.
Bridges, 18th Feb. 1938.