Abstract
Sequence specificity of antibodies to UV-damaged DNA has not been described previously. The antisera investigated here were specific for UV-modified DNA and were absolutely dependent upon the presence of thymine residues. Using a series of oligonucleotides in competition ELISA, increased inhibition was observed with increasing chain length of UV-polythymidylate. A minimum of three adjacent thymines was required for effective inhibition; alone, dimers of thymine were poor antigens. Although UV-irradiated poly(dC) was not antigenic, cytosines could partially replace thymines within the smallest effective epitope (T-T-T) with a high degree of sequence specificity, not previously described. The main epitope induced by UV was formed from adjacent thymines and either a 3' or a 5' pyrimidine.
Original language | English |
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Pages (from-to) | 2517-2521 |
Number of pages | 5 |
Journal | Carcinogenesis |
Volume | 15 |
Issue number | 11 |
DOIs | |
Publication status | Published - Nov 1994 |
Keywords
- sequence specificity
- antibody
- UV-damaged DNA
- UV-modified DNA
- DNA
- UV
- thymine
- UV-polythymidylate
- antigenic
- cytosine
- epitope