A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2R)gsb

General Information
SymbolDmel\Df(2R)gsbSpeciesD. melanogaster
NameFlyBase IDFBab0001966
Feature typechromosomal_deletion
Also Known AsDf(2R)IIX62, Df(2R)gsbIIX62
Computed Breakpoints include 60E9;60F1
Deleted segment60E9--60F1
Sequence coordinates
Member of large scale dataset(s)
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
60E9-60E10;60F1-60F2
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data bk1 hits zip << Tkr << bk2 << Kr
Genetic mapping information
Comments
Deficiency breakpoint within the zip locus.
Proximal breakpoint at -55 to -49 kb and distal breakpoint at +40 to +42.5 kb (Cote et al., 1987), with the proximal breakpoint of Df(2R)SB1 approximately at 0.
 
hide Comments on Cytology
Ref: Nusslein-Volhard et al., 1984, Roux Arch. dev. Biol. 193: 267--282
Left limit of break 1 from polytene analysis (FBrf0046110) Right limit of break 1 from inclusion of zip (FBrf0045941) Left limit of break 2 from inclusion of Tkr (FBrf0046110) Right limit of break 2 from polytene analysis (FBrf0046110)
 
hide Sequence Crossreferences
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Partially deleted / disrupted
Molecular Data
hide Genes NOT Deleted / Disrupted
Complementation Data
Molecular Data
hide Genes Duplicated
Complementation Data
Molecular Data
hide Genes NOT Duplicated
Complementation Data
Molecular Data
hide Related Comments
hide Phenotypic Data
In combination with other aberrations
Ecol\lacZY72 staining of Df(2R)gsb/Df(2R)Kr10 mutants suggests aCC and pCC neurons are not duplicated (contrary to results of FBrf0049834). Df(2R)gsb/Df(2R)Kr10 mutants exhibit duplicated RP2 neurons and lack U and CQ neurons, phenotype can be rescued by gsb+t20.1 (though rescue of U and CQ neurons is incomplete). Posterior commissures are missing or reduced, phenotype varies between segments but no segment is wild type.
No effect on In(1)wm4h position-effect variegation.
Df(2R)gsb/Df(2R)SB1 embryos express gsb but not zip (Cote et al., 1987).
 
NOT in combination with other aberrations
In the embryonic motor system of mutant animals exhibit frequently fused ISN and SN nerve roots but the respective dendritic fields do not appear to intermingle.
Mutant embryos show an increase in apoptotic nuclei in the anterior portion of the segment similar to that seen in wgl-12 and arm8, though the increase in cell death is restricted to the ventral and ventrolateral surface of the embryo. There is also a slight in crease in cell death in the ventral en-expressing cells.
Neuroblast NB5-2 is transformed into MP2.
Homozygotes exhibit duplication of the RP2 lineage due to NB5-3 changing to NB4-2 identity. Simultaneous elimination of gsb rescues the RP2 lineage in 70% of ptcH84 hemisegments. Ectopic expression of P{HS-wg} causes triplication of the RP2 lineage.
Cuticular phenotype is rescued by the construct P{gsb-prd}.
Defective in gonad assembly.
P{gsb+} rescues the cuticle phenotype of Df(2R)gsb homozygotes or heterozygotes with Df(2R)Kr10.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
hide Other Comments
The Df(2R)gsb chromosome may 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), but the eye colour phenotype in the presence of Df(2R)gsb overlaps the eye colour phenotype in a wild-type background so it cannot be unequivocally demonstrated that the deficiency chromosome uncovers a suppressor of telomeric silencing. In addition, any suppression is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by a combination of nonsuppressing deficiencies and deficiencies with suppressors that map to the 2L tip.
Df(2R)ES1/Df(2R)gsb embryos fail to complete dorsal closure.
Distal breakpoint maps to position +40 to +42.5 and the proximal breakpoint to position -55 to -49 on the map of the 60E9-F1 interval.
hide Synonyms & Secondary IDs ( 10 )
Reported As
Symbol Synonym
Df(2R)11X62
Df(2R)gsbzipper
Df(2R)gspIIx62
Name Synonym
Secondary FlyBase IDs
  • FBab0002180
hide References ( 43 )
Generate a list of
List References by type
hide Recent research papers ( 1 )
Liu and Xue, 2012, PLoS ONE 7(1): e30980
Functional Conservation of the Drosophila gooseberry Gene and Its Evolutionary Alleles. [FBrf0217339]
hide Recent reviews (0)
All reviews listed in FlyBase were published before 2011