Allele Dmel\drke0A
| General Information | |||
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| Symbol | Dmel\drke0A | Species | D. melanogaster |
| Name | FlyBase ID | FBal0031081 | |
| Feature type | allele | Associated gene | Dmel\drk |
| Also Known As | drkeOA | ||
| Allele class | antimorphic allele - genetic evidence | ||
| Mutagen | |||
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. | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mutations Mapped to the Genome | |||
Type Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Amino acid replacement: H106Y. | ||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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Detailed Description
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Statement Reference Olfactory association learning is lower in drk[e0A] heterozygotes compared to controls.
Histological and immunohistochemical examination of drk[e0A] heterozygous heads with multiple antigenic markers does not reveal and gross structural anomalies in the brain. Avoidance of odors used as CS and electroshock (US) are no different from that of controls. Heterozygous mutants exhibit normal odor avoidance after pre-exposure to electric shock. Mutation disrupts development of receptor cell R7. Reduces the ability of a cell to develop as an R7 cell or as any other photoreceptor. | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Suppressed by | |||
Statement Reference | |||
Enhancer of | |||
Statement Reference | |||
NOT Enhancer of | |||
Statement Reference drke0A is a non-enhancer of visible phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, btlScer\UAS.T:λ\cI-DD, stumpsScer\UAS.T:Zzzz\FLAG | |||
Suppressor of | |||
Statement Reference | |||
NOT Suppressor of | |||
Statement Reference drke0A is a non-suppressor of visible phenotype of C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3, Scer\GAL4dpp.blk1 drke0A is a non-suppressor of visible phenotype of C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3, Scer\GAL4GMR.PF/Scer\GAL4GMR.PF drke0A is a non-suppressor of visible phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, btlScer\UAS.T:λ\cI-DD, stumpsScer\UAS.T:Zzzz\FLAG | |||
Phenotype Manifest In
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Enhancer of | |||
Statement Reference | |||
NOT Enhancer of | |||
Statement Reference drke0A is a non-enhancer of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, btlScer\UAS.T:λ\cI-DD, stumpsScer\UAS.T:Zzzz\FLAG Scer\GAL4tub.PU/drke0A is a non-enhancer of wing vein phenotype of Scer\GAL4tub.PU, cswY279C.Scer\UAS.P\T | |||
Suppressor of | |||
Statement Reference drk[+]/drke0A is a suppressor of wing vein | ectopic phenotype of Pi3K68DKD.Scer\UAS.T:Hsap\MYC, Scer\GAL469B drk[+]/drke0A is a suppressor of wing vein | ectopic phenotype of Scer\GAL4tub.PU, cswN308D.Scer\UAS.P\T drke0A is a suppressor of phenotype of Src42AKR.hs.2sev | |||
NOT Suppressor of | |||
Statement Reference drke0A is a non-suppressor of eye phenotype of C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3, Scer\GAL4GMR.PF/Scer\GAL4GMR.PF drke0A is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF/Scer\GAL4GMR.PF, btlScer\UAS.T:λ\cI-DD, stumpsScer\UAS.T:Zzzz\FLAG drke0A is a non-suppressor of wing vein L3 phenotype of C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3, Scer\GAL4dpp.blk1 Scer\GAL4tub.PU/drke0A is a non-suppressor of wing vein phenotype of Scer\GAL4tub.PU, cswY279C.Scer\UAS.P\T | |||
Other | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference One copy of drk[e0A] enhances the reduction in wing blade area seen in homozygous sl[2] males.
One copy of drk[e0A] does not enhance the reduction in wing blade area seen in homozygous sl[9] males.
One copy of drk[e0A] partially suppresses the ectopic wing vein phenotype seen in sl[2] homozygotes.
One copy of drk[e0A] partially suppresses the percentage of sl[2] mutant ommatidia that contain extra R7 photoreceptors. drk[e0A]/+ significantly suppresses the ventralised egg shell phenotype observed when Cbl[L.Scer\UAS] is expressed in follicle cells under the control of Scer\GAL4[EQ1].
drk[e0A]/+ fails to suppresses the ventralised egg shell phenotype observed when Cbl[L.mPR.Scer\UAS] is expressed in follicle cells under the control of Scer\GAL4[EQ1].
The dorsalised eggshell phenotype observed when Cbl[L.Δ70Z.Scer\UAS] is expressed under the control of Scer\GAL4[EQ1] is suppressed in a drk[e0A]/+ background. Expression of phl[fl.Scer\UAS] under the control of Scer\GAL4[c747] results in full reversal of the learning deficit of drk[e0A] heterozygotes.
Expression of phl[Scer\UAS.F179] under the control of Scer\GAL4[c747] results in full reversal of the learning deficit of drk[e0A] heterozygotes. The presence of a drk[e0A] background does not affect ectopic wing vein formation in csw[Y279C.Scer\UAS] (Scer\GAL4[tub]) mutants. drk[e0A]/+ suppresses the ectopic wing vein phenotype caused by expression of Pi3K68D[KD.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[69B]. Weakly enhances the eye phenotype produced by activated arm constructs. (either armS44Y.GMR or armS56F.GMR). Has no effect on the eye phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4GMR.PF. Has no effect on the wing vein phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4dpp.blk1. drke0A significantly suppresses the formation of extra outer photoreceptors caused by B-H1sev.PH, although it does not affect the loss of R7 cell phenotype caused by B-H1sev.PH. Presence of the mutation in Src64BΔ540.hs.sev flies alleviates the rough eye phenotype. No effect on the faf eye phenotype. Mutation has no effect on the rough eye phenotype caused by two insertions of P{GMR-Rho1}. Suppression of the rough eye phenotype (formation of extra R7 cells) caused by P{sev-svp2} and enhancement of the P{ro-svp1} rough eye phenotype (loss of one or more outer photoreceptors from many of the ommatidia). | |||
Xenogenetic Interactions
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Statement Reference The penetrance of the Fas2-positive axon crossover phenotype seen in embryos carrying Khc::Ggal\MLCKKA.ftz is increased if they are also homozygous for drke0A. | |||
Complementation & Rescue Data
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| Rescued by | |||
| Comments | |||
Stocks
( 2 ) | |||
| Bloomington | |||
| Kyoto | 108368 | ||
Notes on Origin
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| Discoverer | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
| Linkouts | |||
Synonyms & Secondary IDs
( 8 ) | |||
| Reported As | |||
| Symbol Synonym | drke0A drkeOA drkeoa drkeOa DrkEOA DrkH106Y E(sev)2Be0A | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 20 ) | |||
| Research paper |
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Recent Updates
External Crossreferences & Linkouts