A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Dl3

General Information
SymbolDmel\Dl3SpeciesD. melanogaster
NameFlyBase IDFBal0002460
Feature typealleleAssociated geneDmel\Dl
Allele classloss of function allele
Mutagenspontaneous
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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
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
 
 
Cytology
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Statement
Reference
Heterozygous flies show a mild vein thickening along the length and at the distal tip of wing vein L2, bifurcation of the posterior crossvein at its junction with vein L5, thickening of vein L5 at the distal tip and a thickening of vein L4 at its junction with the anterior crossvein.
The RP2 motoneuron duplicated at the expense of the RP2sib. The aCC motoneuron is duplicated at the expense of the pCC interneuron. The Usib fates are duplicated at the expense of the U neurons. The dMP2 is duplicated at the expense of the vMP2. No change was observable in EL cell fate. This phenotype is the reciprocal of that shown for numb mutants. Mutant embryos show excess neuroblast formation characteristic of neurogenic mutants.
Assymetric division of all the MP2 precursors formed is not altered, but the smaller vMP2 is transformed to the dMP2 fate. In numb1 Dl3 double mutants all MP2 neurons develop as dMP2.
Individuals heterozygous for Bpt1 and heterozygous for Dl3 exhibit no Bpt1 phenotype.
Lethal or semi-lethal when in combination with large deficiency alleles of E(spl) or Df(3R)Espl3. suppressor Extragenic suppressor of the Nspl-1-E(spl)1 interaction.
Dl3 shows similar although less severe phenotypes to Dl1. In contrast to Dl1, Dl3 shows a thickening at the crossveins.
Like Dl1 but deltas at margin are slight; longitudinal veins between anterior and posterior crossveins and crossveins themselves are thickened. Spreading of wing slighter than in Dl1. Better viability than Dl1. homozygous lethal. RK1.
 
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Statement
Reference
Dl3 has visible | dominant phenotype, enhanceable by lqf[+]/lqfARI
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Statement
Reference
Dl3 is an enhancer of visible phenotype of Myt1GMR.PP
hideSuppressor of
Statement
Reference
Dl3 is a suppressor of visible phenotype of osGMR.PB
hideOther
Statement
Reference
Dl3, M(2)31A[+]/M(2)31A1 has viable phenotype
Dl3, M(3)99E1/M(3)99E[+] has viable phenotype
Dl3, RpS3[+]/RpS31 has viable phenotype
Dl3/Dl[+], M(2)31A1 has viable phenotype
Dl3/Dl[+], M(3)96CF1 has lethal | dominant phenotype
Dl3/Dl[+], M(3)99E1 has viable phenotype
Dl3/Dl[+], RpS31 has viable phenotype
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Statement
Reference
Dl3 has posterior crossvein phenotype, enhanceable by lqf[+]/lqfARI
Dl3 has wing vein L2 | distal phenotype, enhanceable by lqf[+]/lqfARI
Dl3 has wing vein L2 phenotype, enhanceable by lqf[+]/lqfARI
Dl3 has wing vein L4 phenotype, enhanceable by lqf[+]/lqfARI
Dl3 has wing vein L5 | distal phenotype, enhanceable by lqf[+]/lqfARI
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Statement
Reference
Dl3 has phenotype, suppressible by S1
Dl3 has wing vein phenotype, suppressible by sno71e3
hideNOT suppressed by
Statement
Reference
Dl3 has phenotype, non-suppressible by Dp(2;3)P
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Statement
Reference
Dl3/Dl[+] is an enhancer of cardioblast | supernumerary phenotype of lqfARI
Dl3 is an enhancer of eye phenotype of Myt1GMR.PP
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Statement
Reference
Dl3 is a suppressor of eye phenotype of osGMR.PB
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Statement
Reference
Dl3, stl[+]/stl4 has ovariole phenotype
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Statement
Reference
96.1% of stl[4]/+ ; Dl[3]/+ ovarioles have compound or morphologically disrupted follicles.
Heterozygosity for Dl3 increases the frequency of lqfARI embryos that show an excess cardioblast phenotype at 18oC. lqfARI dominantly enhances the expressivity and penetrance of all Dl3/+ wing vein phenotypes.
The confluens phenotype of Dl3 is suppressed by sno71e3.
Dl3 is viable in double heterozygous combination with RpS31, M(2)31A1 or M(3)99E1.
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Statement
Reference
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Fails to complement
Rescued by
Partially rescued by
Comments
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Bridges, 10th Dec. 1924.
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hide Synonyms & Secondary IDs ( 2 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
hide References ( 20 )
Research paper
Tsubota et al., 2011, Fly 5(4): 275--284
Interactions between enhancer of rudimentary and Notch and deltex reveal a regulatory function of enhancer of rudimentary in the Notch signaling pathway in Drosophila melanogaster. [FBrf0217950]
Babaoglan et al., 2009, Development 136(24): 4089--4098
Sanpodo: a context-dependent activator and inhibitor of Notch signaling during asymmetric divisions. [FBrf0209326]
Ozdowski et al., 2009, Genetics 183(3): 1027--1040
stall Encodes an ADAMTS Metalloprotease and Interacts Genetically With Delta in Drosophila Ovarian Follicle Formation. [FBrf0209377]
Mukherjee et al., 2006, Genetics 172(3): 1683--1697
Identification of Drosophila genes modulating janus kinase/signal transducer and activator of transcription signal transduction. [FBrf0190752]
Desbordes et al., 2005, Genetics 170(2): 749--766
A screen for genes regulating the wingless gradient in Drosophila embryos. [FBrf0187638]
Tian et al., 2004, Development 131(23): 5807--5815
Epsin potentiates Notch pathway activity in Drosophila and C. elegans. [FBrf0180177]
Price et al., 2002, Genetics 161(2): 721--731
Ectopic expression of the Drosophila Cdk1 inhibitory kinases, wee1 and myt1, interferes with the second mitotic wave and disrupts pattern formation during eye development. [FBrf0149024]
Gurganus et al., 1999, Genetics 152(4): 1585--1604
High-resolution mapping of quantitative trait loci for sternopleural bristle number in Drosophila melanogaster. [FBrf0109835]
Lear et al., 1999, Mech. Dev. 88(2): 207--219
Neural cell fate in rca1 and cycA mutants: the roles of intrinsic and extrinsic factors in asymmetric division in the Drosophila central nervous system. [FBrf0111940]
Lyman and Mackay, 1998, Genetics 149(2): 983--998
Candidate quantitative trait loci and naturally occurring phenotypic variation for bristle number in Drosophila melanogaster. The Delta-Hairless gene region. [FBrf0102969]
Skeath and Doe, 1998, Development 125(10): 1857--1865
Sanpodo and Notch act in opposition to Numb to distinguish sibling neuron fates in the Drosophila CNS. [FBrf0102831]
Long et al., 1996, Genetics 144(4): 1497--1510
Genetic interactions between naturally occurring alleles at quantitative trait loci and mutant alleles at candidate loci affecting bristle number in Drosophila melanogaster. [FBrf0091115]
Spana and Doe, 1996, Neuron 17(1): 21--26
Numb antagonizes Notch signaling to specify sibling neuron cell fates. [FBrf0089976]
Coyle-Thompson and Banerjee, 1993, Development 119(2): 377--395
The strawberry notch gene functions with Notch in common developmental pathways. [FBrf0068459]
Duus et al., 1992, Dev. Biol. 151: 34--47
Blackpatch, a neural degeneration mutation that interacts with the Notch locus in Drosophila. [FBrf0055810]
Alton et al., 1989, Dev. Genet. 10: 261--272
Molecular genetics of Delta, a locus required for ectodermal differentiation in Drosophila. [FBrf0049525]
Shepard et al., 1989, Genetics 122: 429--438
A tripartite interaction among alleles of Notch, Delta, and Enhancer of split during imaginal development of Drosophila melanogaster. [FBrf0049904]
Schultz, 1929, Genetics 14: 366--419
The Minute reaction in the development of Drosophila melanogaster. [FBrf0001812]
Book
Lindsley and Grell, 1968, Publs Carnegie Instn 627: 469pp
Genetic variations of Drosophila melanogaster. [FBrf0020044]
Bridges and Brehme, 1944, Publs Carnegie Instn 552: vii + 257pp
The mutants of Drosophila melanogaster. [FBrf0006100]