A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Aberration Dmel\Df(2L)al

General Information
SymbolDmel\Df(2L)alSpeciesD. melanogaster
NameDeficiency (2L) aristalessFlyBase IDFBab0001692
Feature typechromosomal_deletion
Computed Breakpoints include 21C1;21C7
Deleted segment21C1--21C7
Map ( GBrowse ) Untitled Document

Error

No matching regions found.

Sequence coordinates
2L:300,574..303,911 [+] (Df(2L)al:bk1)
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.
FB2012_01
References
FB2011_10
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
21B7--21B8;[]
21B8-21C1;21C7-21C8
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data U2af38 << bk1 << fs(2)al << bk2 << lwr
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
hide Comments on Cytology
The distal breakpoint of Df(2L)al is about 300kb from the telomere.
Pi3K21B probably overlaps the distal breakpoint.
Left breakpoint is just before 21C1-21C2, right breakpoint is just before 21D1-21D2.
Left limit of break 1 from polytene analysis (FBrf0031322) Right limit of break 1 from inclusion of al (FBrf0006343) Left limit of break 2 from polytene analysis (FBrf0047732) Right limit of break 2 from polytene analysis (FBrf0098232)
 
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
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
Stated to delete or disrupt ds. Aspects of this conclusion subsequently challenged, see FBrf0125086.
hide Phenotypic Data
In combination with other aberrations
Df(2L)al dominantly enhances the transformation of arista to leg phenotype seen in Df(2R)Dll-MP heterozygotes.
No effect on In(1)wm4h position-effect variegation.
Viable in combination with In(2LR)alv.
Df(2L)al/In(2LR)al8 heterozygotes survive poorly; escapers have reduced aristae, broad thoraces, arched wings, incomplete veins and large eyes (Koroshkina and Golubovsky, 1978).
 
NOT in combination with other aberrations
The Df(2L)al chromosome acts as a dominant weak 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(2L)al results in 2.6% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Wild-type clones made in the ovaries of a mutant female, are significantly larger than clones of heterozygous mutant cells. This size difference is greater in clones initiated at 48 hours after egg laying (AEL) than 2 hours AEL.
Homozygous Df(2L)al mutants show an increase in cardial and pericardial cells during embryonic development.
Df(2L)al in combination with a pair of introgressions from D.simulans spanning 30F1-31E7 to 35D7-36A14 Dsim\Int(2L)S and 21A1 to 22D1--23A2 Dsim\Int(2L)D Dsim\Int(2L)D produces fertile male flies. These flies are female sterile.
Macrophages in homozygotes remain very small and round with a much lower phagocytic index (PI) for apoptotic corpses than wild type (0.26 compared to 3.96). Heterozygotes show a PI of about 1.5.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Does not act as a dominant suppressor of Nnd-1.
Strong enhancer of B.
Midgut development of mutant embryos is wild type.
Maternal hemizygosity for Df(2L)al significantly increases post-fertilization embryonic mortality. Paternal hemizygosity has no effect.
Homozygous embryos do not complete head involution and tracheae are disconnected.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Heterozygotes have an extreme Minute phenotype with rough eyes.
Homozygous lethal heterozygous Minute phenotype
 
hide Stocks ( 4 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
E.B. Lewis, 1940.
 
hide Balancer / Genotype Variants of the Aberration
hide Separable Components
hide Other Comments
hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
Name Synonym
Deficiency (2L) aristaless
 
Secondary FlyBase IDs
hide References ( 74 )
Generate a list of
List References by type
hide Recent research papers ( 1 )
Marygold et al., 2011, Fly 5(4): 291--303
Genetic characterization of ebi reveals its critical role in Drosophila wing growth. [FBrf0216882]
hide Recent reviews (0)
All reviews listed in FlyBase were published before 2010