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Nikitina, E.A., Komarova, A.V., Golubkova, E.V., Tret'yakova, I.V., Mamon, L.A. (2003). Semidominant effect of the l(1)ts403 (sbr10) mutation on sex chromosome nondsjunction in meiosis in Drosophila melanogaster females exposed to heat.  Genetika, Moscow 39(3): 341--348.
FlyBase ID
FBrf0167682
Publication Type
Research paper
Abstract
The sbr gene of Drosophila melanogaster belongs to the NXF (nuclear export factor) family responsible for the mRNA transport from nucleus to cytoplasm. We have shown that in the heat-exposed (37 degrees C, 1 h) females, the l(1)ts403 (sbr10) mutation leads, in particular, to the high-frequency nondisjunction and loss of sex chromosomes in meiosis. For this trait, the incomplete dominance of the sbr10 mutation is observed. At the same time, the sbr10 mutation is recessive for many other traits of the heat-exposed flies: reduced viability, low fertility, impaired synthesis of the heat shock proteins, etc. The females heterozygous for the null allele (Df(1)vL4, a deletion eliminating gene srb) do not differ from females homozygous for the wild-type allele in frequency of the heat shock-induced nondisjunction and loss of sex chromosomes in meiosis. Because of this, the sbr10 mutation can be assigned to the gain-of-function alleles (those gaining the dominance function). Expression of the mutant sbr10 allele against the background of the wild-type allele suggests that in the heat shock-exposed females, the heat-modified product of this ts allele has a strong effect on sex chromosome disjunction in meiosis.
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Research paper
Nikitina et al., 2003, Russ. J. Genet. 39(3): 269--275
Semidominant effect of the l(1)ts403 (sbr[10]) mutation on sex chromosome nondsjunction in meiosis in Drosophila melanogaster females exposed to heat. [FBrf0186139]
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Secondary IDs
    Language of Publication
    Russian
    Additional Languages of Abstract
    English
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Genetika, Moscow
    Title
    Genetika
    Publication Year
    1965-
    ISBN/ISSN
    0016-6758
    Data From Reference
    Aberrations (1)
    Alleles (1)
    Genes (1)