Abstract
Labelled RNA preparations (total newly synthesized RNA, as well as stable cytoplasmic RNA) isolated from a cell culture of D. melanogaster were hybridized in situ with polytene chromosomes. Apart from the nucleolus, in all cases the regions adjacent to the chromocentre in the polytene chromosomes and the intercalary heterochromatin regions in the X chromosome and the autosomes are the most intensively labelled. In the case of asynapsis of polytene chromosomes in heterozygotes the label is detected in a number of intercalary heterochromatin sites in one homologue only ("the asymmetrical label"). The same kind of radioactivity distribution in intercalary heterochromatin regions was observed after a hybridization of polytene chromosomes with cloned DNA fragments (Ananiev et al., 1978, 1979) coding for the abundant classes of messenger RNA (Ilyin et al., 1978) in a cultured D. melanogaster cells. In some regions of intercalary heterochromatin which do not contain these fragments the "'asymmetrical" type of label distribution is observed after hybridization with cell RNA. - These results lead one to regard the intercalary heterochromatin regions as "nests" comprising different types of actively transcribable genes, the composition of each nest varying in different stocks of D. melanogaster.
MeSH Terms
Animals
Autoradiography
Cell Nucleolus
Cells, Cultured
Centromere
Chromosomes
Drosophila melanogaster/genetics
Heterochromatin/metabolism
Nucleic Acid Hybridization
RNA/biosynthesis,isolation & purification
Transcription, Genetic
Chemicals
Heterochromatin
RNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gvozdev V A
Ananiev E V
Kotelyanskaya A E
Zhimulev I F
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