Larval glue protein fractions of Drosophila nasuta nasuta were analyzed by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis. Seven major and at least four minor glue protein fractions were recognized. Six of the major fractions are glycosylated. They migrate as three prominent doublets (greater than 100, 43, and 30/28 kd). The synthesis of traceable amounts of these major fractions begins already during the second as well as during the early stages of the third larval instar. The 43-kd and the 30/28-kd fractions are coded by X-chromosomal genes. They are probably clustered within the huge puff of division 10, which is the most prominent X-chromosomal puff in the polytene chromosomes of the third larval instar. Complex posttranslational modification of all but one major glue protein fraction (14 kd) leads to the formation of about 15 different protein fractions in the final glue product. The amount of glue protein produced by D. n. nasuta larvae (in relation to the total saliva proteins) is nearly twice the amount produced by D. melanogaster larvae (ca. 55 and 32%, respectively).
Two types of autosomal mutations have been induced by EMS. One type (enhancer) has the same effect on the zeste phenotype as have additional white subloci, the other (suppressor) acts similar to white subloci deficiencies. Enhancers and suppressors are dominant mutations with recessive lethal effects. Their interactions with different zeste and white alleles are discussed.
Protein fractions of salivary glands were analyzed from 30 wildtype strains of eight species belonging to the Drosophila nasuta subgroup by SDS-polyacrylamide gel electrophoresis. The electrophoretic patterns indicated several prominent bands which could be shown to represent the major glue protein fractions. The glue protein fractions are species-specific as well as wildtype strain-specific. Wildtype strain specificities are characterized by variations of the species-specific patterns. The patterns of the different wildtypes, species, and hybrids were used for taxonomic identification within the nasuta subgroup, in which the females are morphologically indistinguishable and the males differ only by the markings of their frons. The hybrids provide evidence for gonosomal as well as autosomal linkage of individual genes coding for the major glue protein fractions.
SUMMARY
A new type of a Laser Scan Microscope (Zeiss) was used for the analysis of the band‐interband pattern of polytene chromosomes in Chironomus. In contrast to the previously used techniques of transmission light and electron microscopy, we used differential interference contrast (DIC) in incident light to depict the pattern. Instead of using common squash preparations, we carried out this investigation with surface spread polytene (SSP) chromosome preparations of salivary glands. The combination of techniques used enabled a more detailed light microscopic presentation of polytene structures in individual preparations than conventional techniques used so far for chromosome mapping.
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