A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Allele Dmel\Egfrf5

General Information
SymbolDmel\Egfrf5SpeciesD. melanogaster
NameFlyBase IDFBal0003533
Feature typealleleCreated / Updated2006-08-22/2006-08-22
Associated geneDmel\Egfr
Allele classamorph, hypomorph
Mutagenethyl methanesulfonate
hide Nature of the Allele
Allele class
Mutagen
Mapped Features and Mutations
Type
Symbol & 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
      Nucleotide substitution: G926A. Amino acid replacement: W186@. Stop codon is an amber.
      Assay mode
      Cytology
      hide Phenotypic Data
      hide Phenotypic Class
      hide Phenotype Manifest In
      hide Detailed Description
      Statement
      Reference
      severe allele
       
      Homozygotes and hemizygotes display an intermediate 'flb' phenotype. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage.
      Enhances the female sterility and adult morphological defects of Egfrt1. Rarely survives as transheterozygote with the semi-viable Egfrtop-CA allele.
      In mutant embryos, massive cell death occurs in the head. The visual system is almost entirely absent, though the Bolwig's organ remains.
      Egfrf5 stage 11 embryos show domains of cell death in the anterior and posterior parts of the head. The posterior domain covers the optic placode. The apoptosis results in loss of major portions of the head epidermis, so that the brain is exposed in stage 14 embryos. The optic placode has almost disappeared by stage 14. The apoptosis is delayed in the optic placode relative to the apoptosis in the head epidermis. Cell death is also seen in the ventral neuroectoderm at stage 10/11.
      Late stage mutant embryos show a strong reduction in size of the corpus cardiacum compared to wild type and the stomatogastric nervous system is absent.
      hide Interactions
      hide Phenotypic Class
      hide Phenotype Manifest In
      hideSuppressed by
      Statement
      Reference
      Egfrf5 has optic lobe phenotype, suppressible by Df(3L)H99
      hideNOT suppressed by
      Statement
      Reference
      Egfrf5 has phenotype, non-suppressible by eRF1[+]/eRF1F2
      hideSuppressor of
      Statement
      Reference
      hideOther
      Statement
      Reference
      hide Additional Comments
      hide Genetic Interactions
      Statement
      Reference
      The optic lobes are restored in double mutants with Df(3L)H99.
      The optic placode fails to invaginate in Egfrf5 ; Df(3L)H99 embryos, leaving it exposed at the surface of the embryo. Cells that would normally separate from the placode and become the Bolwig's organ remain part of the placode. These cells show a typical epithelial phenotype and are structurally indistinguishable from the surrounding optic lobe cells (although they express neuronal markers). In some cases, outgrowth of short, axon-like processes is seen.
      hide Xenogenetic Interactions
      Statement
      Reference
      hide Complementation & Rescue Data
      Comments
      hide Stocks ( 0 )
      hide Notes on Origin
      Discoverer
      Selected as: Embryonic lethal.
       
      hide Comments
      Mutation of Egfr that coordinately affects all gene activities, a class I lesion. The allelic series for class I lesions: Egfrt2 = Egfrt1 < Egfrtop-EC20 < Egfrf7 = Egfrf1 = Egfrflb-2E07 < Egfrtop-EE39 = Egfrtop-ED26 = Egfrf5 < Egfrf9 = Egfrf10 = Egfrf2 = Egfrtop-EE42 = Egfrf11 = Egfrf24 = Egfrf3 = Df(2R)Egfr3.
      Double mutants for Egfr and sdt or crb show an enhancement of the sdt or crb mutant phenotype.
      hide Synonyms & Secondary IDs ( 6 )
      Reported As
      Symbol Synonym
      Egfrf5
       
      flb
       
      Name Synonym
      faint little ball
       
      Secondary FlyBase IDs
        hide References ( 14 )
        Research paper
        De Velasco et al., 2004, Dev. Biol. 274(2): 280--294
        Embryonic development of the Drosophila corpus cardiacum, a neuroendocrine gland with similarity to the vertebrate pituitary, is controlled by sine oeulis and glass. [FBrf0179777]
        Chang et al., 2003, Dev. Biol. 263(1): 103--113
        Antagonistic relationship between Dpp and EGFR signaling in Drosophila head patterning. [FBrf0173075]
        Chao et al., 2003, Genetics 165(2): 601--612
        Mutations in eukaryotic release factors 1 and 3 act as general nonsense suppressors in Drosophila. [FBrf0167661]
        Dumstrei et al., 2002, Development 129(17): 3983--3994
        Interaction between EGFR signaling and DE-cadherin during nervous system morphogenesis. [FBrf0151275]
        Reich and Shilo, 2002, EMBO J. 21(16): 4287--4296
        Keren, a new ligand of the Drosophila epidermal growth factor receptor, undergoes two modes of cleavage. [FBrf0151286]
        Daniel et al., 1999, Development 126(13): 2945--2954
        The control of cell fate in the embryonic visual system by atonal, tailless and EGFR signaling. [FBrf0108690]
        Dumstrei et al., 1998, Development 125(17): 3417--3426
        EGFR signaling is required for the differentiation and maintenance of neural progenitors along the dorsal midline of the Drosophila embryonic head. [FBrf0104745]
        Clifford and Schupbach, 1994, Genetics 137(2): 531--550
        Molecular analysis of the Drosophila EGF receptor homolog reveals that several genetically defined classes of alleles cluster in subdomains of the receptor protein. [FBrf0072848]
        Tepass and Knust, 1993, Dev. Biol. 159(1): 311--326
        Crumbs and stardust act in a genetic pathway that controls the organization of epithelia in Drosophila melanogaster. [FBrf0058055]
        Raz et al., 1991, Genetics 129: 191--201
        Interallelic complementation among DER/flb alleles: implications for the mechanism of signal transduction by receptor-tyrosine kinases. [FBrf0054136]
        Clifford and Schupbach, 1989, Genetics 123: 771--787
        Coordinately and differentially mutable activities of torpedo, the Drosophila melanogaster homolog of the vertebrate EGF receptor gene. [FBrf0049928]
        Schejter and Shilo, 1989, Cell 56: 1093--1104
        The Drosophila EGF receptor homolog (DER) gene is allelic to faint little ball, a locus essential for embryonic development. [FBrf0049332]
        Nusslein-Volhard et al., 1984, Roux Arch. dev. Biol. 193: 267--282
        Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. [FBrf0041708]
        Stock list
        Tearle and Nusslein-Volhard, 1987, D. I. S. 66: 209--269
        Tubingen mutants and stock list. [FBrf0045941]