A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Allele Dmel\spn-B1

General Information
SymbolDmel\spn-B1SpeciesD. melanogaster
NameFlyBase IDFBal0016033
Feature typealleleCreated / Updated2006-08-22/2006-08-22
Associated geneDmel\spn-B
Allele classamorph
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: G113R.
      Assay mode
      Cytology
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      Statement
      Reference
      maternal-effect lethal. Similar to spn-A but normal eggs also recovered; eggs always unfertilized and abnormal eggs often long.
       
      Hemizygous eggs exhibit either a strong or weak ventralised phenotype: eggs are longer than wild type and are completely symmetric along the DV axis or the eggs display fused dorsal appendages. Egg chambers of females exhibit a partially penetrant disruption in the positioning of the oocyte which can be located anywhere in the egg chamber. Almost all oocytes lack a karyosome and the oocyte chromosomes are arranged instead in thread-like figures with irregular shape. Germline clones in egg chambers are composed of wild type follicle cells, mutant nurse cells, oocytes that give rise to ventralised eggs and oocytes that lack a karyosome.
      Hemizygotes are viable. Eggs derived from fs(1)K10unspecified; spn-B2/spn-B1 females show a broad spectrum of phenotypes ranging from completely dorsalised to completely ventralised. spn-B1/spn-B2 larvae show normal sensitivity to methyl methanesulfonate.
      In contrast to wild-type ovaries, where the synaptonemal complex (SC) is always restricted to the oocyte by region 2b, spn-B1 mutant females show a significant delay in the process, with cysts with more than 1 cell in synapsis in region 3 of the germarium.
      Mutants are weakly sensitive to X ray irradiation when irradiated at either 24-48 or 48-72 hours after egg laying (AEL). Little difference in viability is seen in irradiated at 0-24 hours AEL.
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      hideNOT Enhanced by
      Statement
      Reference
      hideNOT suppressed by
      Statement
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      hideNOT Enhancer of
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      hideNOT Suppressor of
      Statement
      Reference
      spn-B1 is a non-suppressor of radiation sensitive phenotype of spn-A093A
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      Statement
      Reference
      spn-B1 has oocyte phenotype, enhanceable by spn-D2
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      Statement
      Reference
      spn-B1 is an enhancer of oocyte phenotype of spn-D2
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      Statement
      Reference
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      Statement
      Reference
      Double mutants with spn-D2 increases the oocyte mispositioning frequency. Double mutant stage 5-6 egg chambers with mus301094 exhibit a two-oocyte phenotype: the second pro-oocyte develops as an oocyte rather than a nurse cell. The double mutants delay but do not block the decision between the two pro-oocytes as one of the two cells always becomes a nurse cell eventually. Double mutant mothers with fs(1)K101 lay dorsalised eggs, the dorsal appendages form a collar around the entire circumference of the egg. This phenotype is indistinguishable from that of fs(1)K101 single mutants.
      Has no effect on the frequency of X-Y chromosome nondisjunction seen in Df(1)X-1-53B males.
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      Comments
      hide Stocks ( 2 )
      Bloomington
      Kyoto
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      Discoverer
      hide Synonyms & Secondary IDs ( 4 )
      Reported As
      Symbol Synonym
      spn-B1
       
      Name Synonym
      Secondary FlyBase IDs
        hide References ( 8 )
        Research paper
        Findley et al., 2003, Development 130(5): 859--871
        Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage. [FBrf0155724]
        Staeva-Vieira et al., 2003, EMBO J. 22(21): 5863--5874
        An essential role of DmRad51/SpnA in DNA repair and meiotic checkpoint control. [FBrf0167550]
        Huynh and St. Johnston, 2000, Development 127(13): 2785--2794
        The role of BicD, Egl, Orb and the microtubules in the restriction of meiosis to the Drosophila oocyte. [FBrf0128498]
        McKee et al., 2000, Genetica 109(1-2): 77--93
        On the roles of heterochromatin and euchromatin in meiosis in Drosophila: mapping chromosomal pairing sites and testing candidate mutations for effects on X-Y nondisjunction and meiotic drive in male meiosis. [FBrf0135799]
        Pare and Suter, 2000, J. Cell Sci. 113(12): 2119--2127
        Subcellular localization of bic-D::GFP is linked to an asymmetric oocyte nucleus. [FBrf0128601]
        Ghabrial et al., 1998, Genes Dev. 12(17): 2711--2723
        okra and spindle-B encode components of the RAD52 DNA repair pathway and affect meiosis and patterning in Drosophila oogenesis. [FBrf0104438]
        Gonzalez-Reyes et al., 1997, Development 124(24): 4927--4937
        Oocyte determination and the origin of polarity in Drosophila: the role of the spindle genes. [FBrf0100046]
        Stock list
        Tearle and Nusslein-Volhard, 1987, D. I. S. 66: 209--269
        Tubingen mutants and stock list. [FBrf0045941]