Isolation of rat liver 5S RNA genes

A method for the isolation of structural genes, whose transcripts do not contain terminal poly(A) sequences, is presented. Poly(A) tails of predicted length were synthesized at the 3'-OH ends of RNA molecules employing Escherichia coli ATP:RNA adenyltransferase (EC 2.7.7.19). The gene isolation...

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Bibliographic Details
Published inGene Vol. 11; no. 1; pp. 97 - 108
Main Authors Arsenyan, S.G., Avdonina, T.A., Laving, A., Saarma, M., Kisselev, L.L.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.10.1980
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Summary:A method for the isolation of structural genes, whose transcripts do not contain terminal poly(A) sequences, is presented. Poly(A) tails of predicted length were synthesized at the 3'-OH ends of RNA molecules employing Escherichia coli ATP:RNA adenyltransferase (EC 2.7.7.19). The gene isolation was performed in two steps: (a) enrichment of DNA fragments carrying the genes of interest, (b) subsequent cloning and amplification of these fragments. The enrichment of given gene sequences requires separate purifications of each of two complementary DNA chains, followed by their annealing. Rat liver 5S RNA genes were isolated by this method. DNA (+)chains were obtained by hybridizing EcoRI-digested and denatured rat liver DNA fragments with the 5S RNA-poly(A). The complex was purified on an oligo(dT)-cellulose column. DNA (−)chains were purified by hybridizing DNA fragments with the 5 S cDNA which was coupled to oligo(dT)-cellulose. In the isolated and annealed doublestranded DNA preparation the enrichment of 5S DNA was 350–400-fold, when compared with the total genomic DNA. These purified DNA sequences were inserted into the EcoRI site of pBR325. Out of 1200 recombinantplasmid colonies, analyzed in the colony-hybridization test, 4 hybridized with [ 125]5S RNA.
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ISSN:0378-1119
1879-0038
DOI:10.1016/0378-1119(80)90090-6