A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Aberration Dmel\Df(2L)ast4

General Information
SymbolDmel\Df(2L)ast4SpeciesD. melanogaster
NameDeficiency (2L) asteroidFlyBase IDFBab0001697
Feature typechromosomal_deletion
Computed Breakpoints include 21D1-21D2;21E2
Deleted segment21D1--21E2
Sequence coordinates
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
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
21D1-21D2;21E1-21E2
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data bk1 << l(2)21Dg << l(2)21Dd << bk2
Genetic mapping information
Comments
hide Comments on Cytology
Limits of break 1 from polytene analysis (FBrf0042627) Left limit of break 2 from inclusion of ast (FBrf0042627) Right limit of break 2 from polytene analysis (FBrf0042627)
 
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
hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Df(2L)ast4 heterozygotes have a missing-bract phenotype (17% of bracts in the tibia and 78% in the basitarsus of the second leg remain).
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(2L)ast4 chromosome acts as a dominant moderate 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 this is assumed to be a false positive result (the suppressor may not be within the bounds of the deficient region) because the 2L TAS array on the chromosome is missing (as assayed by in situ hybridization) and it has previously been shown (FBrf0137248, FBrf0158986) that partial or complete deficiency of the 2L TAS array on the homologue suppresses silencing of brown-red variants of P{3'WP-2,wvar}2Lt. In addition, the deficiency chromosome fails to complement lethal mutations of l(2)gl and deficiencies that are mutant for l(2)gl are often also deficient for the 2L TAS array (FBrf0137248).
hide Synonyms & Secondary IDs ( 5 )
Reported As
Symbol Synonym
Df(2L)ast4
 
Name Synonym
Deficiency (2L) asteroid
 
Secondary FlyBase IDs
hide References ( 9 )
Research paper
Marrus et al., 2004, J. Neurosci. 24(6): 1406--1415
Differential localization of glutamate receptor subunits at the Drosophila neuromuscular junction. [FBrf0174850]
Mason et al., 2004, Genetics 168(3): 1353--1370
A deficiency screen for dominant suppressors of telomeric silencing in Drosophila. [FBrf0180277]
Artero et al., 2003, Development 130(25): 6257--6272
Notch and Ras signaling pathway effector genes expressed in fusion competent and founder cells during Drosophila myogenesis. [FBrf0167513]
Held, 2002, Mech. Dev. 117(1-2): 225--234
Bristles induce bracts via the EGFR pathway on Drosophila legs. [FBrf0152194]
Chan et al., 2001, Molec. Biol. Cell 12(5): 1409--1419
Dribble, the Drosophila KRR1p homologue, is involved in rRNA processing. [FBrf0137029]
Schneuwly et al., 1989, Proc. Natl. Acad. Sci. USA 86: 5390--5394
Drosophila ninaA gene encodes an eye-specific cyclophilin (cyclosporine A binding protein). [FBrf0050847]
Roberts et al., 1985, Genetics 109: 145--156
A genetic and cytogenetic analysis of the region surrounding the LSP-1 gene of Drosophila melanogaster. [FBrf0042627]
FlyBase analysis
FlyBase, 2007, En masse symbol-based assigment of Aberration Class with respect to wild type.
En masse symbol-based assigment of Aberration Class with respect to wild type. [FBrf0191808]
Book
Lindsley and Zimm, 1992, The Genome of Drosophila melanogaster.
The Genome of Drosophila melanogaster. [FBrf0066905]