Abstract
The lambdagt clones containing fragments of the Drosophila melanogaster genome were prepared and characterized by hybridization of their DNA with (I) lambdagt-cRNA; (2) lambdaC-cRNA; (3) Dm-cRNA; (4) the mRNA of D.melanogaster culture cells and (5) the stable cytoplasmic poly (A) RNA from the same source. The technique for a simple selection of hybrid clones is described. The hybridization with mRNA allows one to select the clones containing structural genes of D.melanogaster. It was found that in all cases when the clone contains the structural gene it also contains the reiterated base sequences of the D.melanogaster genome. Several clones containing D. melanogaster DNA fragments with a size of (2-4)x1O6 daltons hybridizing with a relatively large portion of mRNA were selected for further analysis.
MeSH Terms
Animals
Clone Cells
Coliphages/metabolism
DNA/metabolism
DNA, Recombinant
DNA, Viral/metabolism
Drosophila melanogaster/metabolism
Genes
Nucleic Acid Hybridization
Poly A/metabolism
RNA, Messenger/metabolism
Recombination, Genetic
Selection, Genetic
Transformation, Genetic
Chemicals
DNA, Recombinant
DNA, Viral
RNA, Messenger
Poly A
DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ilyin Y V
Tchurikov N A
Georgiev
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