A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\fz1

General Information
SymbolDmel\fz1SpeciesD. melanogaster
NameFlyBase IDFBal0004917
Feature typealleleAssociated geneDmel\fz
Allele classhypomorphic allele - genetic evidence
Mutagenspontaneous
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
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Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
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UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
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Cytology
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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
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Statement
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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
 
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Reference
fz1 has bract phenotype, non-enhanceable by fy1
fz1 has bract phenotype, non-enhanceable by in1
fz1 has joint phenotype, non-enhanceable by fy1
fz1 has joint phenotype, non-enhanceable by in1
fz1 has tarsal segment phenotype, non-enhanceable by fy1
fz1 has tarsal segment phenotype, non-enhanceable by in1
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Statement
Reference
fz1 has wing disc | P-stage phenotype, suppressible by fy1
fz1 has wing disc | P-stage phenotype, suppressible by in1
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Statement
Reference
fz1 has bract phenotype, non-suppressible by fy1
fz1 has bract phenotype, non-suppressible by in1
fz1 has eye phenotype, non-suppressible by fy1
fz1 has eye phenotype, non-suppressible by in1
fz1 has joint phenotype, non-suppressible by fy1
fz1 has joint phenotype, non-suppressible by in1
fz1 has microchaeta & adult thorax | somatic clone | cell non-autonomous phenotype, non-suppressible 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
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Reference
fz1 is a non-suppressor of microchaeta & adult thorax phenotype of fy1
fz1 is a non-suppressor of microchaeta & adult thorax phenotype of in1
fz1 is a non-suppressor of ommatidium phenotype of Rac1V12.hs.sev
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Reference
drlR343 ; fz1 double mutants have a higher penetrance of salivary gland curving than is seen in either of the single mutants alone.
Domineering non-autonomy of fz1 clones is not suppressed by in1. Leg phenotypes of fz1 and fy1 or in1 are additive.
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.
In double mutant combinations between VangA3, VangA5 and VangTbs42 with fz1, fz25 and fz30, the fz-in type of polarity pattern was slightly less abnormal than in either single mutant.
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Partially rescued by
Partially rescues
Comments
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.
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Bloomington
Kyoto
106445
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Discoverer
Bridges, 18th Feb. 1938.
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