A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\perBG.T:Ppyr\LUC

General Information
SymbolDmel\perBG.T:Ppyr\LUCSpeciesD. melanogaster
NameFlyBase IDFBal0063147
Feature typealleleAssociated geneDmel\per
Allele class
Mutagenin 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
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Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
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Progenitor genotype
Nature of the lesion
Statement
Reference
Construct: Fusion of a 9.8kb BamHI per fragment extending from -4200 to +5627 to a 1.8kb BamHI-KpnI Ppyr\LUC cDNA. Expression is influenced by 1kb EcoRI fragment carring the SV40 polyadenylation site. Two thirds of the per protein is fused in frame to the Ppyr\LUC cDNA.
Carried in construct
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Cytology
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Statement
Reference
Flies expressing perBG.T:Ppyr\LUC are able to entrain to a 12 hour:12 hour LD cycle at 25oC. These flies entrain to a 12 hour:12 hour 25oC:18oC temperature cycle in LL but exhibit maximum activity during the middle of the warm phase, while the wild-type activity peak is at the end of the warm phase and extends into the phase. perBG.T:Ppyr\LUC flies can also entrain to two consecutive warm:cold cycles in LL where the second cycle is phase advanced by 6 hours; they reach a new stable phase relationship after 3-4 days by steadily advancing their average activity peak during the warm phase.
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Statement
Reference
Flies expressing perBG.T:Ppyr\LUC in a nocte1 background are able to entrain to a 12 hour:12 hour LD cycle at 25oC. In contrast to wild-type flies, perBG.T:Ppyr\LUC nocte1 flies fail to entrain to a 12 hour:12 hour 25oC:18oC temperature cycle in LL; these flies are constantly active throughout both temperatures, except for a drop in activity during a ~1 hour window shortly after transition to the cold phase. Activity levels are higher in the warm phase. Further, the flies fail to entrain to two consecutive warm:cold cycles in LL where the second cycle is phase advanced by 6 hours, instead they abruptly change their activity level at the time of temperature transition. The flies behave similarly to control flies when kept in constant darkness at a variety of constant temperatures.
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Reported As
Symbol Synonym
LUC::perBG
 
perBG.T:Ppyr\LUC
 
Name Synonym
Secondary FlyBase IDs
hide References ( 16 )
Research paper
Hung et al., 2009, J. Biol. Rhythms 24(3): 183--192
HSP90, a Capacitor of Behavioral Variation. [FBrf0207993]
Sehadova et al., 2009, Neuron 64(2): 251--266
Temperature entrainment of Drosophila's circadian clock involves the gene nocte and signaling from peripheral sensory tissues to the brain. [FBrf0209187]
Dolezelova et al., 2007, Genetics 177(1): 329--345
Rhythm defects caused by newly engineered null mutations in Drosophila's cryptochrome gene. [FBrf0201773]
Zheng et al., 2007, Proc. Natl. Acad. Sci. U.S.A. 104(40): 15899--15904
FOXO and insulin signaling regulate sensitivity of the circadian clock to oxidative stress. [FBrf0216135]
Koh et al., 2006, Science 312(5781): 1809--1812
JETLAG resets the Drosophila circadian clock by promoting light-induced degradation of TIMELESS. [FBrf0193019]
Glaser and Stanewsky, 2005, Curr. Biol. 15(15): 1352--1363
Temperature synchronization of the Drosophila circadian clock. [FBrf0187310]
Wuelbeck et al., 2005, Genetics 169(2): 751--766
The novel Drosophila tim(blind) mutation affects behavioral rhythms but not periodic eclosion. [FBrf0187663]
Yuan et al., 2005, Neuron 47(1): 115--127
Serotonin modulates circadian entrainment in Drosophila. [FBrf0188183]
Stanewsky et al., 2002, J. Biol. Rhythms 17(4): 293--306
Mapping of elements involved in regulating normal temporal period and timeless RNA expression patterns in Drosophila melanogaster. [FBrf0151362]
Helfrich-Forster et al., 2001, Neuron 30(1): 249--261
The circadian clock of fruit flies is blind after elimination of all known photoreceptors. [FBrf0135910]
Krishnan et al., 2001, Nature 411(6835): 313--317
A new role for cryptochrome in a Drosophila circadian oscillator. [FBrf0135900]
Giebultowicz et al., 2000, Curr. Biol. 10(2): 107--110
Transplanted Drosophila excretory tubules maintain circadian clock cycling out of phase with the host. [FBrf0125137]
Kaneko et al., 2000, J. Neurobiol. 43(3): 207--233
Disruption of synaptic transmission or clock-gene-product oscillations in circadian pacemaker cells of Drosophila cause abnormal behavioral rhythms. [FBrf0128517]
Belvin et al., 1999, Neuron 22(4): 777--787
The Drosophila dCREB2 gene affects the circadian clock. [FBrf0108141]
Stanewsky et al., 1998, Cell 95(5): 681--692
The cryb mutation identifies cryptochrome as a circadian photoreceptor in Drosophila. [FBrf0105937]
Stanewsky et al., 1997, EMBO J. 16(16): 5006--5018
Multiple circadian-regulated elements contribute to cycling period gene expression in Drosophila. [FBrf0096339]