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  • 1980-1984  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 195 (1984), S. 434-441 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Measurement of dopa decarboxylase (DDC) levels in 109 strains of Drosophila melanogaster isogenic for second chromosomes isolated independently from natural populations was undertaken. One of the most extreme variants, designated Ddc +4, was shown to have about 20% more DDC activity at adult eclosion than a standard laboratory strain used for comparison. The DDC overproduction was shown to segregate with the second chromosome and was mapped to a position within 0.15 map units of the DDC structural gene. The variant was shown to be an underproducer of DDC activity at pupariation and the genetic element responsible for this trait mapped in an identical fashion to that causing overproduction. The temporal phenotype described above was observed in the epidermis but DDC activity levels in neural tissue were normal. Examination of CRM levels at pupariation and eclosion revealed that altered DDC protein levels were responsible for the variant DDC activity levels. Electrophoretic analysis under both denaturing and non-denaturing conditions indicated that the DDC molecules in Ddc +4 and the laboratory strain were indistinguishable. These results suggest that alterations in a genetic element (or elements) lying in close proximity to the structural gene are responsible for the complex temporal phenotype of DDC activity exhibited in the variant Ddc +4.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 195 (1984), S. 442-451 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An activity variant in Drosophila, Ddc +4, which has been isolated from natural populations is shown to affect the level of messenger RNA for dopa decarboxylase (DDC) in a stage specific manner. Newly hatched first instar larvae and newly eclosed adults have 1.5 times the amount of DDC mRNA as the Canton-S laboratory strain. On the other hand, puparia of the variant have only 0.5 times as much DDC mRNA as Canton-S. Genomic Southern analysis revealed that Ddc +4 DNA differed from Canton-S DNA by four small restriction length polymorphisms. To confirm these differences, a library of Ddc +4 was constructed in the λ1059 vector. A clone was recovered spanning the DDC region and compared to cloned Canton-S DNA. Acrylamide gel electrophoresis of restriction fragments revealed that one previously identified insertion really consisted of two smaller ones. One of the other differences identified by the Southern analysis was not confirmed in the cloned DNA of Ddc +4, indicating some divergence had occurred in the variant strain between the time of its isogenization and cloning. The differences between the cloned Ddc +4 DNA and cloned Canton-S DNA consisted of six small restriction length polymorphisms and one restriction site polymorphism. Five of the seven differences lay in the 5′ untranslated leader sequence of the DDC mRNA or in the 4.5 kb of DNA upstream of the transcription start site. The existence of these small (〈100 bp) insertion/deletion polymorphisms in a strain exhibiting a complex temporal phenotype for DDC activity, suggests natural populations are an excellent source of variation affecting gene expression. Secondly, subtle restriction length polymorphisms near the 5′ end of genes may well be an important component of the variation upon which selection might be expected to act.
    Type of Medium: Electronic Resource
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