A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Recombinant construct P{UAS-DnaJ-1.K}

General Information
Symbol P{UAS-DnaJ-1.K} FlyBase ID FBtp0012543
Feature type transgenic_transposon
Size Expression data
Associated insertions 1 available
Molecular map
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Description
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FB2013_03
FB2013_02
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hide Description & Uses
Species synthetic construct
Location-dependent
role
Description
CV term
Qualifiers & info
Reference
transposon
Uses
CV term
Qualifiers & info
Reference
binary system (targeted)
characterization
Cloning Sites
Location
Restriction sites
Reference
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Sequence (FB)
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Extent
 
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Total Size
Left end
Right end
Segments
Number
Orientation
Symbol
Reference
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CV term
Qualifiers & info
Reference
hide Component Alleles
Allele DnaJ-1Scer\UAS.cKa
Reference(s) (Kazemi-Esfarjani and Benzer, 2000, Takeyama et al., 2002, Tsai et al., 2004, Chartier et al., 2006, Wang et al., 2012, Fayazi et al., 2006, Ghosh and Feany, 2004, Nisoli et al., 2010, Doumanis et al., 2009, Nishimura et al., 2010)
Molecular data
Construct: Scer\UAS regulatory sequences drive expression of DnaJ-1 coding sequences.
Phenotypic class
Phenotype manifest in
Other information
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects expression of
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progenitor(s)
descendant(s)
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Bloomington
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Other Crossreferences
Linkouts
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Reported As
Symbol Synonym
P{UAS-dHdj1}
P{UAS-DnaJ-1.K}
UAS-dhdj-1
UAS-dhdj1
UAS-dHdj1
UAS-DNAJ1
Secondary FlyBase IDs
hide References ( 11 )
Research paper
Wang et al., 2012, Aging Cell 11(1): 93--103
Reduced neuronal expression of ribose-5-phosphate isomerase enhances tolerance to oxidative stress, extends lifespan, and attenuates polyglutamine toxicity in Drosophila. [FBrf0217184]
Nishimura et al., 2010, J. Neurogenet. 24(4): 194--206
Selection of Behaviors and Segmental Coordination During Larval Locomotion Is Disrupted by Nuclear Polyglutamine Inclusions in a New Drosophila Huntington's Disease-Like Model. [FBrf0212327]
Nisoli et al., 2010, Cell Death Differ. 17(10): 1577--1587
Neurodegeneration by polyglutamine Atrophin is not rescued by induction of autophagy. [FBrf0212035]
Doumanis et al., 2009, PLoS ONE 4(9): e7275
RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation. [FBrf0209128]
Chartier et al., 2006, EMBO J. 25(10): 2253--2262
A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1. [FBrf0190356]
Fayazi et al., 2006, Neurobiol. Disease 24(2): 226--244
A Drosophila ortholog of the human MRJ modulates polyglutamine toxicity and aggregation. [FBrf0193414]
Ghosh and Feany, 2004, Hum. Mol. Genet. 13(18): 2011--2018
Comparison of pathways controlling toxicity in the eye and brain in Drosophila models of human neurodegenerative diseases. [FBrf0180337]
Tsai et al., 2004, Proc. Natl. Acad. Sci. U.S.A. 101(12): 4047--4052
Ataxin 1, a SCA1 neurodegenerative disorder protein, is functionally linked to the silencing mediator of retinoid and thyroid hormone receptors. [FBrf0175091]
Takeyama et al., 2002, Neuron 35(5): 855--864
Androgen-dependent neurodegeneration by polyglutamine-expanded human androgen receptor in Drosophila. [FBrf0152267]
Kazemi-Esfarjani and Benzer, 2000, Science 287(5459): 1837--1840
Genetic suppression of polyglutamine toxicity in Drosophila. [FBrf0126796]
Personal communication to FlyBase
Kazemi-Esfarjani, 2010.5.11, UAS-DnaJ-1.K insertion from Parsa Kazemi-Esfarjani.
UAS-DnaJ-1.K insertion from Parsa Kazemi-Esfarjani. [FBrf0210715]