A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Su(H)IB115

General Information
SymbolDmel\Su(H)IB115SpeciesD. melanogaster
NameFlyBase IDFBal0039061
Feature typealleleAssociated geneDmel\Su(H)
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0034030 FBal0058207 FBal0034031 FBal0039061 FBal0016317 FBal0016307
Allele classloss of function allele, amorphic allele - genetic evidence
Mutagenethyl methanesulfonate
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
point mutation
pr_change=K138@
na_change=A15041122T
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Nonsense mutation in codon 138.
Nucleotide substitution: A1226T. Amino acid replacement: K94@.
Cytology
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Statement
Reference
The number of corpora cardiaca cells is normal in mutant embryos.
Su(H)[1]/Su(H)[IB115] mutant tissues exhibit a loss of ptc-positive prohemocytes and the overproduction of differentiated plasmatocytes. By contrast, an increase is not observed in the crystal cell population in Su(H)[1]/Su(H)[IB115] mutant lymph glands.
Homozygotes are lethal during pupal development. Heterozygous flies carrying out 10 training sessions to test memory of odours display a lower 24 hour memory in spaced training (rest periods between tasks) compared to control flies.
No effect on the faf eye phenotype.
Su(H)8/Su(H)IB115 wings are reduced to stumps.
Lethality during the first day of pupal development. Supernumerary cells stained in mutant imaginal discs have adopted a sensory organ precursor (SOP) fate instead of the epidermal fate they would normally express. The excess SOPs arise from the proneural clusters of potential precursor cels that appear in the imaginal discs during the development of wild type bristles. The wing pouch region of the wing imaginal disc and the retinal field of the eye-antennal imaginal disc are dramatically reduced. Identical phenotype is seen when transheterozygous with Df(2L)TE35BC-24, Su(H)1, Su(H)2 or Su(H)8.
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Linkouts
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hideEnhancer of
Statement
Reference
Su(H)[+]/Su(H)IB115 is an enhancer of visible | dominant phenotype of NMcd1
Su(H)[+]/Su(H)IB115 is an enhancer of visible | dominant phenotype of NMcd5
hideSuppressor of
Statement
Reference
Su(H)IB115 is a suppressor of visible phenotype of Nact.sev
hideOther
Statement
Reference
hide Phenotype Manifest In
hideEnhancer of
Statement
Reference
Su(H)[+]/Su(H)IB115 is an enhancer of adult thorax & microchaeta phenotype of NMcd1
Su(H)[+]/Su(H)IB115 is an enhancer of adult thorax & microchaeta phenotype of NMcd5
hideSuppressor of
Statement
Reference
Su(H)IB115 is a suppressor of phenotype of H1
hideOther
Statement
Reference
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hide Genetic Interactions
Statement
Reference
Su(H)IB115 dominantly enhances the loss of microchaetae seen in NMcd1, NMcd5 or NMcd8 heterozygotes, reducing the number of microchaetae per heminotum to 64.00 +/- 1.84, 69.92 +/- 1.86 or 79.67 +/- 1.40 respectively.
Mutation has no detectable effect on the rough eye phenotypes of NANK.sev.
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Statement
Reference
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Rescued by
Comments
Neurogenic and lethal phenotype can be fully rescued by Su(H)+t6.0.
hide Stocks ( 1 )
Bloomington
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Discoverer
hide Comments
Has no effect the phenotype of Nl1N-ts1/Nfa-g62.
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Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 1 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
  • FBal0034029
hide References ( 15 )
Research paper
Park et al., 2011, PLoS Genet. 7(8): e1002241
Specification of Drosophila corpora cardiaca neuroendocrine cells from mesoderm is regulated by Notch signaling. [FBrf0215231]
Tokusumi et al., 2010, Development 137(21): 3561--3568
Serpent, suppressor of hairless and U-shaped are crucial regulators of hedgehog niche expression and prohemocyte maintenance during Drosophila larval hematopoiesis. [FBrf0212074]
Song et al., 2009, J. Neurogenet. 23(4): 405--411
Suppressor of Hairless Is Required for Long-Term Memory Formation in Drosophila. [FBrf0210464]
Ramain et al., 2001, Curr. Biol. 11(22): 1729--1738
Novel Notch alleles reveal a Deltex-dependent pathway repressing neural fate. [FBrf0141440]
Matsuno et al., 1997, Development 124(21): 4265--4273
Suppressor of Hairless-independent events in Notch signaling imply novel pathway elements. [FBrf0099385]
Gho et al., 1996, Development 122(6): 1673--1682
Subcellular localization of Suppressor of Hairless in Drosophila sense organ cells during Notch signalling. [FBrf0088148]
Huang and Fischer-Vize, 1996, Development 122(10): 3207--3216
Undifferentiated cells in the developing Drosophila eye influence facet assembly and require the Fat facets ubiquitin-specific protease. [FBrf0090618]
Leviten and Posakony, 1996, Dev. Biol. 176(2): 264--283
Gain-of-function alleles of Bearded interfere with alternative cell fate decisions in Drosophila adult sensory organ development. [FBrf0088401]
Verheyen et al., 1996, Genetics 144(3): 1127--1141
Analysis of dominant enhancers and suppressors of activated Notch in Drosophila. [FBrf0090844]
Couso et al., 1995, Curr. Biol. 5(12): 1437--1448
Serrate and wingless cooperate to induce vestigial gene expression and wing formation in Drosophila. [FBrf0084908]
Fortini and Artavanis-Tsakonas, 1994, Cell 79(2): 273--282
The suppressor of Hairless protein participates in Notch receptor signaling. [FBrf0076038]
Schweisguth et al., 1994, Dev. Biol. 166(2): 812--814
The sequence similarity of the Drosophila Suppressor of Hairless protein to the integrase domain has no functional significance in vivo. [FBrf0079374]
Furukawa et al., 1992, Cell 69: 1191--1197
The Drosophila homolog of the immunoglobulin recombination signal-binding protein regulates peripheral nervous system development. [FBrf0055544]
Schweisguth and Posakony, 1992, Cell 69: 1199--1212
Suppressor of Hairless, the Drosophila homolog of the mouse recombination signal-binding protein gene, controls sensory organ cell fates. [FBrf0055545]
Personal communication to FlyBase
Ashburner et al., 1999.10.12, Adh.
Adh. [FBrf0112153]