
In the present investigation chromosomal preparations of Asellus aquaticus were sequentially stained with chromomycin A3 to reveal the heterochromatic areas, hybridized in situ with rDNA probes in order to map the ribosomal genes and finally silver stained to check the transcriptional activity of these genes. The results indicate the existence of a substantial correspondence of location and size among the heterochromatic regions and the regions over which the in situ hybridization signals spread. The ribosomal genes, quite independently of their location in the secondary constriction, can be silver stained and thus appear to be transcriptionally active. The ribosomal sequences also hybridize to the entire heterochromatic areas observed on the probable Y chromosome identified in some males of a natural population. These rRNA genes are only rarely transcriptionally active.
Male, Silver Staining, Chromosome Mapping, DNA, Ribosomal, Genes, RNA, Ribosomal, Crustacea, Heterochromatin, Nucleolus Organizer Region, Animals, In Situ Hybridization, Fluorescence
Male, Silver Staining, Chromosome Mapping, DNA, Ribosomal, Genes, RNA, Ribosomal, Crustacea, Heterochromatin, Nucleolus Organizer Region, Animals, In Situ Hybridization, Fluorescence
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