Abstract
DNA preparations from about hundred randomly selected clones containing mouse DNA fragments were screened for the existence of sequences complementary to long double-stranded regions of pre-mRNA able to snap back after melting (dsRNA-B). Many clones containing such sequences were found. The cloned sequences can be subdivided into three groups: (1) those complementary to about a half (at least to 30-40%) of the total dsRNA, designated as sequences B1; (2) those complementary to a part of sequence B1; and (3) sequences complementary to about a quarter (at least to 15%) of the total dsRNA referred to as sequence B2. The size of DNA sequence complementary to dsRNA is about 400 base pairs. Melting experiments with hybrids show that the members of B1 family are very similar if not identical, while the divergence among B2 sequences is higher, but still the number of substitutions does not exceed 9% of bases. Thus, the major part of dsRNA-B consists of a small number of highly abundant sequences as was suggested earlier on the basis of renaturation kinetics /1-3/. Sequences B1 and B2 are represented by many copies in the mouse genome and in pre-mRNA, and many of them probably do not form hairpin-like structures.
MeSH Terms
Animals
Base Sequence
Carcinoma, Ehrlich Tumor/metabolism
Cell Nucleus/metabolism
DNA, Recombinant/metabolism
Escherichia coli/metabolism
Mice
Nucleic Acid Denaturation
Nucleic Acid Hybridization
Plasmids
RNA, Messenger/biosynthesis
RNA, Neoplasm/metabolism
Chemicals
DNA, Recombinant
RNA, Messenger
RNA, Neoplasm
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kramerov D A
Grigoryan A A
Ryskov A P
Georgiev G P
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