A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Zzzz\CAGQ108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG

General Information
SymbolZzzz\CAGQ108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAGSpeciesa. artificial
NameFlyBase IDFBal0137335
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
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Associated Sequence Data
DDBJ /
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DNA sequence
Protein sequence
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Nature of the lesion
Statement
Reference
Construct: Scer\UAS regulatory sequences drive expression of a polyglutamine repeat tagged with T:Hsap\MYC and T:Zzzz\FLAG.
Scer\UAS regulatory sequences drive expression of a 108 amino acid polyglutamine repeat (the repeat is flanked by the amino acid sequence MRSRKL at the N-terminal end and by KLRS at the C-terminal end). The T:Hsap\MYC and T:Zzzz\FLAG tags are present at the C-terminal end of the open reading frame (immediately after the KLRS sequence).
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Cytology
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Statement
Reference
Expression of Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] in the eye under the control of Scer\GAL4[GMR.PF] causes depigmentation.
Expression of Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[elav-C155] results in dramatic pre-adult lethality, which is partially rescued by Li[+].
Expression of Zzzz\CAGQ108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG under the control of Scer\GAL4elav.PLu results in degeneration of neurons in the eye, as indicated by large gaps in the eye tissue and loss of rhabdomeres. Each ommatidium contains on average only 3 neurons in these eyes (compared to 7 in wild type).
Adult survivors expressing Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[dpp.blk1] often have a split thorax phenotype. Adult survivors expressing Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[GMR.PF] have a rough eye with no pigment. Adult survivors expressing Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[hs.2sev] show a loss of large sensory bristles. External eye morphology is normal in adults expressing Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[elav.PU]. However, many of the ommatidia contain only four to six rhabdomeres. Gaps are evident in the retinal tissue. Adults expressing Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] under the control of Scer\GAL4[elav.PU] have a shortened lifespan compared to wild type.
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Reference
Expression of lok[Scer\UAS.cPa] does not enhance the eye depigmentation phenotype seen when Zzzz\CAG[Q108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG] is expressed 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\CAGQ108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG under the control of Scer\GAL4elav.PLu.
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Reported As
Symbol Synonym
Zzzz\CAGQ108.Scer\UAS.T:Hsap\MYC,T:Zzzz\FLAG
 
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hide References ( 4 )
Research paper
Iijima-Ando et al., 2010, Hum. Mol. Genet. 19(10): 1930--1938
A DNA damage-activated checkpoint kinase phosphorylates tau and enhances tau-induced neurodegeneration. [FBrf0210684]
Berger et al., 2005, Hum. Mol. Genet. 14(20): 3003--3011
Lithium rescues toxicity of aggregate-prone proteins in Drosophila by perturbing Wnt pathway. [FBrf0190825]
Kazantsev et al., 2002, Nat. Genet. 30(4): 367--376
A bivalent Huntingtin binding peptide suppresses polyglutamine aggregation and pathogenesis in Drosophila. [FBrf0147171]
Marsh et al., 2000, Hum. Mol. Genet. 9(1): 13--25
Expanded polyglutamine peptides alone are intrinsically cytotoxic and cause neurodegeneration in Drosophila. [FBrf0123123]