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Sequence analysis of heteropolymeric DNA synthesized in vitro by the enzyme terminal deoxy-nucleotidyl transferase and cloned inEscherichia coli
Author(s) -
Giuseppe Damiani,
A. Ivana Scovassi,
Simona Romagnoli,
Emanuela Palla,
Umberto Bertazzoni,
V. Sgaramella
Publication year - 1982
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/10.20.6401
Subject(s) - biology , terminal deoxynucleotidyl transferase , primer (cosmetics) , transferase , microbiology and biotechnology , plasmid , nucleotide , escherichia coli , dna , recombinant dna , biochemistry , nucleic acid sequence , complementary dna , enzyme , gene , chemistry , apoptosis , organic chemistry , tunel assay
We have synthesized in vitro single strands of DNA in reaction mixtures containing the terminal deoxynucleotidyl transferase (Bollum's enzyme), an oligo-dG as primer, the four common deoxynucleoside triphosphates and both Mg and Co ions. The resulting heteropolymers have been converted into double strands, tailed with oligo-dC sequences, annealed with an oligo-dG tailed plasmid vector and cloned in E. coli. Six recombinant plasmids have been isolated and characterized. Two of them have been sequenced. The heteropolymeric chains produced by the terminal transferase, ranging in size between 200 and 400 nucleotides, are richer in purines than in pyrimidines, except in the last portions. Open reading frames for 7-20 amino acids with repeated, in phase translational stop codons are present in these sequences and in their complements.

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