A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2L)pr-A14

General Information
SymbolDmel\Df(2L)pr-A14SpeciesD. melanogaster
NameDeficiency (2L) purpleFlyBase IDFBab0001867
Feature typechromosomal_deletion
Also Known AsDf(2L)A14
Computed Breakpoints include 37D2-37D5;39A4-39A7
Deleted segment37D2--39A7
Sequence coordinates
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
37C6-37D1;39A4-39A7
37D2-37D7;39A4-39A7
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data l(2)37Da << bk1 << l(2)37Db <<βInt-ν << bk2 << crc
Genetic mapping information
Comments
hide Comments on Cytology
Ref: Lindsley and Zimm, 1992
Left limit of break 1 from polytene analysis (FBrf0080145) Right limit of break 1 from inclusion of RanGap (FBrf0030142) Limits of break 2 from polytene analysis (FBrf0080145)
 
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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
Analysis of two-cell mutant clones in the sensory organ precursors of the leg indicates that bract induction is normal when the inner (sheath and neuron) cells are mutant, and that bracts are not induced when the outer cells (shaft and socket) are mutant. Most single-cell mutant clones fail to induce bract cells, while single-cell mutant clones in the shaft cell have no effect on bract cell induction.
Shows no maternal enhancement of dpphr4.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
hide Balancer / Genotype Variants of the Aberration
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hide Other Comments
The Df(2L)pr-A14 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), but this 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 one or more nonsuppressing deficiencies.
hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
Df(2L)prA-14
Name Synonym
Deficiency (2L) purple
 
Secondary FlyBase IDs
hide References ( 20 )
Research paper
Peng et al., 2012, Dev. Cell 23(3): 507--518
Planar Polarized Protrusions Break the Symmetry of EGFR Signaling during Drosophila Bract Cell Fate Induction. [FBrf0219458]
Casso et al., 2008, Genetics 178(3): 1399--1413
A screen for modifiers of hedgehog signaling in Drosophila melanogaster identifies swm and mts. [FBrf0205418]
Ni et al., 2008, J. Neurosci. 28(50): 13478--13487
Mutation of a TADR protein leads to rhodopsin and Gq-dependent retinal degeneration in Drosophila. [FBrf0206556]
Crest et al., 2007, Genetics 175(2): 567--584
Onset of the DNA replication checkpoint in the early Drosophila embryo. [FBrf0194644]
Mason et al., 2004, Genetics 168(3): 1353--1370
A deficiency screen for dominant suppressors of telomeric silencing in Drosophila. [FBrf0180277]
Ward et al., 2003, Genetics 165(3): 1397--1415
Genetic modifier screens in Drosophila demonstrate a role for Rho1 signaling in ecdysone-triggered imaginal disc morphogenesis. [FBrf0167639]
Frolov et al., 2001, Genes Dev. 15(16): 2146--2160
Functional antagonism between E2F family members. [FBrf0138394]
Semeshin et al., 1999, D. I. S. 82: 63--65
Cytological localization of Drosophila melanogaster Dhr38 gene. [FBrf0112033]
Nicholls and Gelbart, 1998, Genetics 149(1): 203--215
Identification of chromosomal regions involved in decapentaplegic function in Drosophila. [FBrf0102843]
Bhadra et al., 1997, Genetics 146(3): 903--917
A sex-influenced modifier in Drosophila that affects a broad spectrum of target loci including the histone repeats. [FBrf0094158]
Kania et al., 1995, Genetics 139(4): 1663--1678
P-element mutations affecting embryonic peripheral nervous system development in Drosophila melanogaster. [FBrf0080145]
Stathakis et al., 1995, Genetics 141(2): 629--655
The genetic and molecular organization of the Dopa decarboxylase gene cluster of Drosophila melanogaster. [FBrf0084402]
Tio et al., 1994, Mech. Dev. 48(1): 13--23
spitz, a Drosophila homolog of transforming growth factor-, is required in the founding photoreceptor cells of the compound eye facets. [FBrf0079521]
Gay and Contamine, 1993, Mol. Gen. Genet. 239(3): 361--370
Study of the ref(2)P locus of Drosophila melanogaster. [FBrf0059083]
Reuter et al., 1993, Development 119(4): 1135--1145
A role for the mesoderm in endodermal migration and morphogenesis in Drosophila. [FBrf0068651]
Ganetzky, 1977, Genetics 86: 321--355
On the components of Segregation Distortion in Drosophila melanogaster. [FBrf0030142]
Personal communication to FlyBase
Roote, 1996.9.11, tup<up>1</up>.
tup1. [FBrf0089933]
BDGP Project Members, 1994-1999, BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file)
BDGP Project Members, 1994-1999, Berkeley Drosophila Genome Project. (Computer file) [FBrf0067338]
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]