Dmel\PBac{WH}DopRf02676 Insertion
| General Information | |||
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| 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 (
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| 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.
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Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Detailed Mapping Data
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| Chromosome (arm) |
3R
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| Sequence Location |
3R:10,032,116..10,032,116 [+]
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| Orientation |
+
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Cytological location
(computed by FlyBase) |
88A11 ( inferred by FlyBase from sequence location )
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Cytological location
(reported) |
88A11 (reported as inferred from sequence location)
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Comments concerning
location |
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Sequence Data
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| Flanking sequence | |||
Inserted Element
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| Construct | PBac{WH} | ||
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Location-dependent
role |
deletion generation component
mobile activating element
carries FRT site(s)
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| Size | 7.234Kb | ||
| Associated alleles | |||
| Molecular map | |||
Affected Gene(s)
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Insertion may
affect gene |
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Alleles and Phenotypes
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| Causes alleles | |||
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Lethality
References
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Sterility
References
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Phenotype Manifest In
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Detailed Description
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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.
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Expression Data
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| Reporter Expression | |||
| Additional Information | |||
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Statement
Reference
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| Marker for | |||
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Reflects
expression of |
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Reporter construct
used in assay |
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External Images
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| FlyView (LinkOut) | |||
Data on Genetic Line
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| Line ID | |||
| Origin as a multiple insertion line | |||
Progenitor(s) within the Genome
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Related Aberration or Balancer
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| Aberration | |||
| Balancer | |||
Stocks
( 1 )
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| Harvard | |||
Linkouts
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Comments
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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.
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Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
f02676
PBac{WH}DopRf02676
PBac{WH}f02676
UAS-DopR1
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| Secondary FlyBase IDs | |||
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References
( 14 )
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| Research paper |
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| Supplementary material |
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| Personal communication to FlyBase |
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| FlyBase analysis |
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