A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Aberration Dmel\Df(2R)cn83c

General Information
SymbolDmel\Df(2R)cn83cSpeciesD. melanogaster
NameDeficiency (2R) cinnabarFlyBase IDFBab0002120
Feature typechromosomal_deletionCreated / Updated2006-08-22/2006-08-22
Formalized genetic data bk1 << dpld << sax << bk2
Sequence coordinates
Deleted segment43C5--44C1
Duplicated segment
Computed Breakpoints include 43C5;44B6-44C1
Breakpoints Inherited  
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
43C5;44B6-44C1
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
hide Comments on Cytology
All limits from polytene analysis (FBrf0074016)
 
hide Molecularly Mapped Breakpoints
 
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
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hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Homozygous embryos have smaller heads than normal, and have abnormal tracheae and segmentation. The midgut is smaller than normal, does not constrict and the midgut primordia do not fuse in some embryos. The hindgut and Malpighian tubules are variable in length and crinkled.
Large ventral cord cells.
hide Position Effect Variegation Data
  
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Recovered as apparent cn double recombinants from test crosses of dysgenic-type males that were heterozygous for a maternally derived dp b cn bw second chromosome and paternally derived autosomes extracted from natural populations and capable of promoting male recombination.
 
hide Balancer / Genotype Variants of the Aberration
    hide Separable Components
      hide Other Comments
      The Df(2R)cn83c 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)cn83c 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 one or more nonsuppressing deficiencies.
      hide Synonyms & Secondary IDs ( 3 )
      Reported As
      Symbol Synonym
      Df(2R)cn83c
       
      Name Synonym
      Deficiency (2R) cinnabar
       
      Secondary FlyBase IDs
        hide References ( 14 )
        Research paper
        Mason et al., 2004, Genetics 168(3): 1353--1370
        A deficiency screen for dominant suppressors of telomeric silencing in Drosophila. [FBrf0180277]
        Elmore and Smith, 2001, Insect Biochem. Molec. Biol. 31(8): 791--798
        Putative Drosophila odor receptor OR43b localizes to dendrites of olfactory neurons. [FBrf0136968]
        Firth et al., 2000, Genetics 156(2): 733--748
        Identification of genomic regions that interact with a viable allele of the Drosophila protein tyrosine phosphatase corkscrew. [FBrf0129810]
        Duffy et al., 1996, Genetics 142(3): 839--852
        Dosage-sensitive maternal modifiers of the Drosophila segmentation gene runt. [FBrf0086390]
        Rodriguez et al., 1996, Genetics 143(2): 929--940
        Identification of immune system and responses genes, and novel mutations causing melanotic tumor formation in Drosophila melanogaster. [FBrf0087676]
        Harbecke and Lengyel, 1995, Roux Arch. dev. Biol. 204(5): 308--329
        Genes controlling posterior gut development in the Drosophila embryo. [FBrf0082073]
        Pauli et al., 1995, Genetics 139(2): 713--732
        Identification of regions interacting with ovo<up>D</up> mutations: Potential new genes involved in germline sex determination or differentiation in Drosophila melanogaster. [FBrf0080317]
        Pauli et al., 1995, D. I. S. 76: 107--124
        Dose dependent enhancers and suppressors of ovoD2. [FBrf0082455]
        Landecker et al., 1994, Dev. Genet. 15(5): 425--434
        Screen for enhancers of Polycomb and Polycomblike in Drosophila melanogaster. [FBrf0076124]
        Nellen et al., 1994, Cell 78(2): 225--237
        Receptor serine/threonine kinases implicated in the control of Drosophila body pattern by decapentaplegic. [FBrf0074016]
        Smith et al., 1993, Genetics 135(3): 817--829
        Identification of genomic regions required for DNA replication during Drosophila embryogenesis. [FBrf0065574]
        Personal communication to FlyBase
        Kimbrell, 1996.4.28, [title not yet available]
        [title not yet available] [FBrf0086748]
        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]