A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3R)ry615

General Information
SymbolDmel\Df(3R)ry615SpeciesD. melanogaster
NameDeficiency (3R) rosyFlyBase IDFBab0002910
Feature typechromosomal_deletion
Also Known AsDf(3R)ry615, ry615
Computed Breakpoints include 87B12;87E8
Deleted segment87B10--87E8 (Estimated cytology)
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Sequence coordinates
3R:8,269,381..8,272,656 (Df(3R)ry615:bk1)
3R:9,181,043..9,190,877 (Df(3R)ry615:bk2)
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
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hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
 
Class of aberration (relative to progenitor)
Breakpoints
87B12-87B15;87E8-87E11
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data l(3)87Bh << bk1 << l(3)87Bm << Ace << bk2 << l(3)05137
Genetic mapping information
Comments
hide Comments on Cytology
The left Df(3R)ry615 breakpoint lies within desat1 (FBgn0086687) in the range 3R:8269381..8272656 (R5) (predicted cytology: 87B10-87B11).
The right Df(3R)ry615 breakpoint lies within mthl12 or CG8790 or in the region between them, and lies in the range 3R:9181043..9190877 (R5) (predicted cytology: 87E7-87E8).
Left limit of break 1 from polytene analysis (FBrf0028767) Right limit of break 1 from polytene analysis (FBrf0076870) Left limit of break 2 from polytene analysis (FBrf0028767) Right limit of break 2 from non-inclusion of l(3)05137 (FBrf0067338)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
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Complementation Data
Completely deleted / disrupted
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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In combination with other aberrations
Does not suppress variegation of the w gene seen in In(1)wm4 animals.
NOT in combination with other aberrations
When P{P-Sal}Pak3[P-Sal] is present, the w gene of the P{lacW}ciDplac insertion variegates, resulting (in a w- background) in an eye that is mostly white with a few patches of red ommatidia. This P-element-dependent silencing of P{lacW}ciDplac is dominantly suppressed by Df(3R)ry615.
The Df(3R)ry615 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Heterozygosity for Df(3R)ry615 results in 0.9% X chromosome nondisjunction and 0.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Homozygous embryos show a "blimp" phenotype (when the embryos are mechanically devitellinised the resulting cuticle preparations stretch to a greater extent than wild-type cuticles).
Heterozygotes show a quantitative effect on wing shape in intervein region C compared to wild type.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Mutation does not affect the level of w expression in ph-plac+3 flies.
Homozygous embryos are very abnormal compared to wild-type.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
'Sloppy' ventral cord.
hide Stocks ( 2 )
Bloomington
Kyoto
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Discoverer
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hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
Name Synonym
Deficiency (3R) rosy
 
Secondary FlyBase IDs
hide References ( 55 )
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hide Recent research papers ( 1 )
Ghabrial et al., 2011, PLoS Genet. 7(7): e1002087
A systematic screen for tube morphogenesis and branching genes in the Drosophila tracheal system. [FBrf0214368]
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All reviews listed in FlyBase were published before 2011