A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Zzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG

General Information
SymbolZzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAGSpeciesa. artificial
NameFlyBase IDFBal0127243
Feature typealleleAssociated geneZzzz\CAG
Allele class
Mutagenin vitro construct - regulatory fusionin vitro construct - coding region fusion
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
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Progenitor genotype
Nature of the lesion
Statement
Reference
Construct: Scer\UAS sequences drive expression of 48 Glutamines. This is tagged with T:Hsap\MYC and T:Zzzz\FLAG.
Carried in construct
Tagged with
Cytology
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eye photoreceptor cell & neuron, with Scer\GAL4elav.PLu
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Statement
Reference
Expression of Zzzz\CAG[Q48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] in photoreceptors under the control of Scer\GAL4[GMR.PF] results in electroretinogram depolarisation amplitudes that are 55% lower than controls.
Flies expressing Zzzz\CAG[Q48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[Eaat1.PR] have a shortened lifespan compared to wild type and are found to be lethargic a few days before dying.
Expression of Zzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG under the control of Scer\GAL4elav.PLu results in loss of 1-2 photoreceptor neurons per ommatidium and some gaps in the eye tissue.
Expression of Zzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG driven by Scer\GAL4elav.PLu leads to degeneration of rhabdomeres and partial lethality. Suberoylanilide hydroxamic acid (SAHA) suppresses the lethality and reduces the level of degeneration seen in the eye to wild-type levels.
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Statement
Reference
Co-expression of Mmus\Cd8a[Scer\UAS.T:Avic\GFP] does not enhance the reduction in electroretinogram depolarisation amplitude seen when Zzzz\CAG[Q48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] is expressed in photoreceptors under the control of Scer\GAL4[GMR.PF]. Co-expression of Dap160[Scer\UAS.cKa] enhances the reduction in electroretinogram depolarisation amplitude seen when Zzzz\CAG[Q48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] is expressed in photoreceptors under the control of Scer\GAL4[GMR.PF].
Co-expression of Hsap\HDSu3.Scer\UAS.T:Zzzz\CAG,T:Hsap\MYC significantly suppresses the loss of photoreceptor neurons seen in flies expressing Zzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG under the control of Scer\GAL4elav.PLu.
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Reported As
Symbol Synonym
Zzzz\CAGQ48.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG
 
Name Synonym
Secondary FlyBase IDs
hide References ( 5 )
Research paper
Scappini et al., 2007, Hum. Mol. Genet. 16(15): 1862--1871
Intersectin enhances huntingtin aggregation and neurodegeneration through activation of c-Jun-NH2-terminal kinase. [FBrf0201221]
Lievens et al., 2005, Hum. Mol. Genet. 14(5): 713--724
Expanded polyglutamine peptides disrupt EGF receptor signaling and glutamate transporter expression in Drosophila. [FBrf0184022]
Apostol et al., 2003, Proc. Natl. Acad. Sci. U.S.A. 100(10): 5950--5955
A cell-based assay for aggregation inhibitors as therapeutics of polyglutamine-repeat disease and validation in Drosophila. [FBrf0159306]
Kazantsev et al., 2002, Nat. Genet. 30(4): 367--376
A bivalent Huntingtin binding peptide suppresses polyglutamine aggregation and pathogenesis in Drosophila. [FBrf0147171]
Steffan et al., 2001, Nature 413(6857): 739--743
Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila. [FBrf0139769]