Conformation of oligonucleotides and nucleic acids modified with 2-aminofluorene or 2-acetylaminofluorene
Author(s) -
Pascale Rio,
Bernard Malfoy,
Évelyne Sage,
Marc Leng
Publication year - 1983
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.8349117
Subject(s) - oligonucleotide , circular dichroism , chemistry , nucleic acid , guanine , dna , fluorescence , antibody , biochemistry , microbiology and biotechnology , stereochemistry , nucleotide , biology , physics , quantum mechanics , gene , immunology
The first part of this work deals with the thermal stability of oligonucleotides modified with acetylaminofluorene and aminofluorene, respectively. The complementary oligonucleotides d(CGCG), d(CGTACG) and d(AATTGCAATT) have been studied by ultraviolet absorption and circular dichroism. In high salt concentration and at low temperature, the three oligonucleotides form double-stranded helices which have the B-form Substitution of guanine residues in these oligonucleotides by acetylated or deacetylated aminofluorene residues destablizes the B-form and does not induce the transition to the Z-form. The second part of the work deals with the antibodies to Z-DNA. The specificity of these antibodies has been determined by radioimmunoassay. The antibodies react with the Z-form but not with the B-form. Poly(dG-dC).poly(dG-dC) modified by acetylaminofluorene residues is recognized by the antibodies. The antibodies can detect the Z-form in natural DNA as visualized by fluorescent staining of polytene chromosomes from Drosophila melanogaster.
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