A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Dmel\PBac{WH}DopRf02676 Insertion

General Information
Symbol Dmel\PBac{WH}DopRf02676 Species D. melanogaster
Name FlyBase ID FBti0050754
Feature type transposable_element_insertion_site
Description
Inserted element PBac{WH} Expression data
Affected gene(s) DopR Viability / fertility
Causes allele(s) DopRf02676 Stock availability 1 publicly available
LINE ID f02676
Genomic Location
Chromosomal location 3R ( 88A11 ) Sequence location 3R:10,032,116..10,032,116 [+]
Map ( GBrowse ) GBrowse View Help detailed view FBti0019374 FBti0050754 FBti0151364 FBti0126082_2 FBti0126082_1
Member of Large Scale Dataset(s)
Dataset

A set of transgenic insertion stocks derived by TE mobilization using the Tni\piggyBac-based construct PBac{WH}. The PBac{WH} construct carries the w[+mC] mini-white marker, a single long (199-bp) Scer\FRT site, and a terminal Scer\UAS site for Scer\GAL4-driven misexpression of adjacent genes. The FRT site allows Scer\FLP-mediated recombination between other FRT-containing elements, and thus can be used to generate molecularly defined deletions.
PBac{WH} insertion lines from Exelixis were remapped and assessed for inclusion in the Gene Disruption Project collection; flanking sequence data were submitted to GenBank.
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Detailed Mapping Data
Chromosome (arm)
Sequence Location
3R:10,032,116..10,032,116 [+]
Orientation
Cytological location
(computed by FlyBase)
88A11 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
88A11 (reported as inferred from sequence location)
Comments concerning
location
hide Sequence Data
Flanking sequence
hide Inserted Element
Construct PBac{WH}
Location-dependent
role
deletion generation component
mobile activating element
carries FRT site(s)
Size 7.234Kb
Associated alleles
Molecular map
hide Affected Gene(s)
Insertion may
affect gene
hide Alleles and Phenotypes
Causes alleles
Lethality
References
Sterility
References
hide Phenotype Manifest In
hide Detailed Description
Statement
Reference
Expressing DopR[f02676] in Gr5a gustatory receptor neurons under the control of Scer\GAL4[Gr5a.8.5] rescues the defects in the sugar-sensitive proboscis extension reflex (PER) seen in DopR[f02676] mutant females.
DopR[f02676] mutant flies show a similar increase in sugar sensitivity in response to L-Dopa feeding to wild controls.
Expression of DopR (from the Scer\UAS sequences in the PBac{WH}DopR[f02676] insertion) under the control of either Scer\GAL4[104Y] or Scer\GAL4[c205] significantly restores the the reduced sleep caused by dopamine signaling in DopR[f02676]/DopR[f02676] flies fed L-dopa. This effect is not seen if expression is driven either by Scer\GAL4[ey-OK107] or by Scer\GAL4[c547].
The decreased night-time sleep seen when wild-type flies are fed L-dopa is markedly suppressed in a DopR[f02676]/DopR[f02676] background.
The reduction in nighttime sleep seen in flies expressing TrpA1[Scer\UAS.cKa] under the control of Scer\GAL4[ple.PF] at 27[o]C is fully suppressed by DopR[f02676]/DopR[f02676].
Flies of the genotype Scer\GAL4[5.30]/+; DopR[f02676]/DopR[f02676] show selectively restored expression of DopR. Those flies that had restored expression in patterns that include the R2/R4 class ellipsoid body neurons exhibit rescue of ethanol-induced hyperactivity. Restoring DopR expression in the R3 neurons of the ellipsoid body neurons (through Scer\GAL4[lilli-189Y]) results in a modest but statistically significant increase in ethanol-induced hyperactivity. However, expression with Scer\GAL4[Aph-4-c232] has no effect on ethanol induced hyperactivity in DopR[f02676] homozygous mutants.
DopR[f02676] mutants show reduced ethanol-induced hyperactivity and no change in ethanol sedation sensitivity or ethanol absorption. DopR[f02676] also show increased activity prior to ethanol exposure. DopR[f02676]/Df(3R)ED5634 flies show reduced ethanol-induced hyperactivity. DopR[f02676] mutants perform indistinguishably from wild-type in a rapid tolerance paradigm, showing both increased ethanol-induced hyperactivity and increased resistance to the sedating effects of ethanol during a second exposure to ethanol vapor.
The failure of DopR[f02676]/In(3LR)234 or DopR[f02676]/DopR[f02676] adults to learn to avoid specific odors after conditioning by concurrent shock and odor exposure is partially rescued by Scer\GAL4[elav-C155] and completely rescued by Scer\GAL4[Mef2.247]. Scer\GAL4[elav-C155] and Scer\GAL4[Mef2.247] also completely rescued learning by sugar-reward conditioning in these flies. (In all cases, rescue was tested in the presence of Scer\GAL80[ts.αTub84B] and rescued was seen at 30\'C but not at room temperature.)
DopR[f02676]/DopR[f02676] and DopR[f02676]/In(3LR)234 adults fail to learn to avoid specific odors after conditioning by concurrent shock and odor exposure. The same results are seen when testing is done immediately after conditioning or 1 hour after conditioning and with a variety of odors. These animals also have significantly reduced scores in tests for sugar reward mediated olfactory conditioning.
hide Expression Data
Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
Reporter construct
used in assay
hide External Images
FlyView (LinkOut)
hide Data on Genetic Line
Line ID
Origin as a multiple insertion line
hide Progenitor(s) within the Genome
hide Related Aberration or Balancer
Aberration
Balancer
hide Stocks ( 1 )
Harvard
hide Linkouts
hide Comments
Location 3R:10032116-10032117 confirmed by FlyBase alignment of dbGSS accession CZ485220 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation confirmed.
hide Synonyms & Secondary IDs
Reported As
Symbol Synonym
PBac{WH}DopRf02676
PBac{WH}f02676
UAS-DopR1
Secondary FlyBase IDs
hide References ( 14 )
Research paper
Inagaki et al., 2012, Cell 148(3): 583--595
Visualizing Neuromodulation In Vivo: TANGO-Mapping of Dopamine Signaling Reveals Appetite Control of Sugar Sensing. [FBrf0217362]
Liu et al., 2012, Curr. Biol. 22(22): 2114--2123
Two dopaminergic neurons signal to the dorsal fan-shaped body to promote wakefulness in Drosophila. [FBrf0220041]
Bellen et al., 2011, Genetics 188(3): 731--743
The Drosophila gene disruption project: progress using transposons with distinctive site specificities. [FBrf0214229]
Kong et al., 2010, PLoS ONE 5(4): e9954
A pair of dopamine neurons target the D1-like dopamine receptor DopR in the central complex to promote ethanol-stimulated locomotion in Drosophila. [FBrf0210514]
Kim et al., 2007, J. Neurosci. 27(29): 7640--7647
D1 dopamine receptor dDA1 is required in the mushroom body neurons for aversive and appetitive learning in Drosophila. [FBrf0202085]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Thibault et al., 2004, Nat. Genet. 36(3): 283--287
A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac. [FBrf0175002]
Supplementary material
Thibault, 2004, Nature Genetics 36(3):
Supplementary Table 3. [FBrf0174228]
Personal communication to FlyBase
Christensen et al., 2008.4.15, Isolation and characterization of Df(3R)BSC470.
Isolation and characterization of Df(3R)BSC470. [FBrf0204548]
Gene Disruption Project members and Exelixis, 2005, Genomic mapping of Exelixis insertion collection. (Computer file)
Genomic mapping of Exelixis insertion collection. (Computer file) [FBrf0184340]
Gene Disruption Project members, 2001-, (Computer file)
(Computer file) [FBrf0132177]
FlyBase analysis
FlyBase Curators, 2013, Members of Exelixis insertion collections: P{XP}, PBac{PB}, PBac{RB}, PBac{WH}.
Members of Exelixis insertion collections: P{XP}, PBac{PB}, PBac{RB}, PBac{WH}. [FBrf0221061]
FlyBase, 2005, Assessment of transgenic construct insertion sites.
Assessment of transgenic construct insertion sites. [FBrf0184339]
FlyBase, 1992-, FlyBase curation.
FlyBase curation. [FBrf0105495]