A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Allele Dmel\Med1

General Information
SymbolDmel\Med1SpeciesD. melanogaster
NameFlyBase IDFBal0011292
Feature typealleleCreated / Updated2006-08-22/2006-08-22
Associated geneDmel\Med
Allele class
Mutagenethyl methanesulfonate
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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
      Amino acid replacement: Q283@.
      Assay mode
      Cytology
      Polytene chromosomes apparently normal.
       
      hide Phenotypic Data
      hide Phenotypic Class
      hide Phenotype Manifest In
      larval head & embryo
      hide Detailed Description
      Statement
      Reference
      imaginal discs missing weak effect on mitotic chromosome condensation Homozygous larvae contain rudimentary imaginal discs, but disc primordia do not grow during larval development; testes and ovaries smaller than normal and cell number in central nervous system reduced. Mutant gonads do not survive metamorphosis when implanted into wild-type larvae. Homozygous cuticular clones appear to develop normally, but with reduced frequency and size compared to control clones. Mutant larvae support growth of implanted wild-type discs. Normal gene product postulated to be required for cell proliferation; survival of somatic epidermal clones attributed to perdurance. Larval ganglion mitoses exhibit weak effect on chromosome condensation as well as chromosome breakage (Gatti and Baker, 1989);
       
      Imaginal discs of homozygous larvae are missing or degenerate. Defects in the cell cycle: few or no dividing cells and affects chromosome condensation.
      Late larval early pupal lethality. Reduction in the number of mitosis in the larval brain (FBrf0049822).
      Embryos lacking maternal and zygotic Med function (Med1/Med25 embryos derived from females with homozygous Med1 germ line clones) show loss of dorsal tissue, expansion of the lateral denticle bands into dorsal regions and severe head defects. The phenotype is partially paternally rescuable. Homozygous clones in the eye are only seen at the margins of the eye, most commonly at the posterior margin, and result in loss of eye tissue.
      Mutant stage 17 embryos do not show significant defects in the location or formation of the tracheal dorsal trunk branch, dorsal branch 10, spiracular branch 10 or the posterior spiracle.
      Med1 zygotic mutant embryos occasionally have dorsal defects.
      hide Interactions
      hide Phenotypic Class
      hideNOT Enhanced by
      Statement
      Reference
      Med1 has lethal | recessive phenotype, non-enhanceable by lilliunspecified
      hideSuppressor of
      Statement
      Reference
      Med[+]/Med1 is a suppressor of visible phenotype of tkvSC143
      Med[+]/Med1 is a suppressor of visible phenotype of Scer\GAL4en-e16E, saxQ263D.Scer\UAS.cDa
      Med[+]/Med1 is a suppressor of visible phenotype of Scer\GAL4A9, gbbScer\UAS.cKa
      Med[+]/Med1 is a suppressor of visible phenotype of Scer\GAL4A9, dppScer\UAS.cHa
      hideOther
      Statement
      Reference
      Med[+]/Med1, dpphr27 has lethal | dominant phenotype
      hide Phenotype Manifest In
      hideEnhancer of
      Statement
      Reference
      Med1 is an enhancer of phenotype of dpphr4
      hideSuppressor of
      Statement
      Reference
      Med[+]/Med1 is a suppressor of wing phenotype of tkvSC143
      Med[+]/Med1 is a suppressor of wing | posterior phenotype of Scer\GAL4en-e16E, saxQ263D.Scer\UAS.cDa
      Med[+]/Med1 is a suppressor of wing vein phenotype of Scer\GAL4A9, gbbScer\UAS.cKa
      Med[+]/Med1 is a suppressor of wing phenotype of Scer\GAL4A9, dppScer\UAS.cHa
      hide Additional Comments
      hide Genetic Interactions
      Statement
      Reference
      Maternal lethal interaction with dpphr4 is due to a loss of dorsal-most fates in the embryos, demonstrated by loss of amnioserosa cells.
      Slightly suppresses the wing phenotype produced by tkvSC143. Shows a dominant maternal effect interaction with dpp; when Med1/+ females are crossed to dpphr27/+ males, all progeny carrying dpphr27 die. This lethality is rescued by MedUbi-p63E.PD also partly by MadUbi-p63E.T:Hsap\MYC.
      hide Xenogenetic Interactions
      Statement
      Reference
      hide Complementation & Rescue Data
      Fails to complement
      Comments
      hide Stocks ( 1 )
      Bloomington
      hide Notes on Origin
      Discoverer
      hide Synonyms & Secondary IDs ( 4 )
      Reported As
      Symbol Synonym
      l(3)12m137
       
      l(3)SG701
       
      Name Synonym
      Secondary FlyBase IDs
        hide References ( 14 )
        Research paper
        Bangi and Wharton, 2006, Development 133(17): 3295--3303
        Dual function of the Drosophila Alk1/Alk2 ortholog Saxophone shapes the Bmp activity gradient in the wing imaginal disc. [FBrf0194511]
        Johnson et al., 2003, Dev. Biol. 262(1): 137--151
        Embryonic enhancers in the dpp disk region regulate a second round of Dpp signaling from the dorsal ectoderm to the mesoderm that represses Zfh-1 expression in a subset of pericardial cells. [FBrf0173104]
        Sutherland et al., 2003, Development 130(23): 5705--5716
        Stepwise formation of a SMAD activity gradient during dorsal-ventral patterning of the Drosophila embryo. [FBrf0167503]
        Newfeld and Takaesu, 2002, Genetics 161(2): 685--692
        An analysis using the hobo genetic system reveals that combinatorial signaling by the Dpp and Wg Pathways regulates dpp expression in leading edge cells of the dorsal ectoderm in Drosophila melanogaster. [FBrf0149021]
        Takaesu et al., 2002, Dev. Biol. 247(2): 225--236
        Combinatorial signaling by an unconventional Wg Pathway and the Dpp pathway requires Nejire (CBP/p300) to regulate dpp expression in posterior tracheal branches. [FBrf0148942]
        Dequier et al., 2001, Mech. Dev. 106(1-2): 47--60
        Top-DER- and Dpp-dependent requirements for the Drosophila fos/kayak gene in follicular epithelium morphogenesis. [FBrf0137300]
        Su et al., 2001, Genetics 157(2): 717--725
        A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's Lymphoma family of transcription factors in Drosophila melanogaster. [FBrf0132343]
        Jazwinska et al., 1999, Development 126(15): 3323--3334
        The role of brinker in mediating the graded response to Dpp in early Drosophila embryos. [FBrf0109999]
        Das et al., 1998, Development 125(8): 1519--1528
        The Drosophila gene Medea demonstrates the requirement for different classes of Smads in dpp signaling. [FBrf0102615]
        Wisotzkey et al., 1998, Development 125(8): 1433--1445
        Medea is a Drosophila Smad4 homolog that is differentially required to potentiate DPP responses. [FBrf0102610]
        Raftery et al., 1995, Genetics 139(1): 241--254
        Genetic screens to identify elements of the decapentaplegic signaling pathway in Drosophila. [FBrf0079237]
        Gatti and Baker, 1989, Genes Dev. 3: 438--453
        Genes controlling essential cell-cycle functions in Drosophila melanogaster. [FBrf0049822]
        Personal communication to FlyBase
        Cook, 2006.1.31, Characterization of deletions and Minutes in chromosomal region 99-100.
        Characterization of deletions and Minutes in chromosomal region 99-100. [FBrf0191633]
        Raftery, 1995.4.6, [title not yet available]
        [title not yet available] [FBrf0086254]