Damage induced by a single psoralen-modified triple helix-forming olig
onucleotide has been reported to be efficiently repaired in human cell
s, In this study we investigated a set of psoralen coupled oligonucleo
tides introducing multiple lesions into the target DNA. A simian virus
40 (SV40) shuttle vector was in vitro treated with different triple h
elix-forming oligonucleotides and UVA radiation, leading to double pso
ralen adducts at the supF mutational target gene of the plasmid, After
passage in the Rail human cell line the recovered vector was analysed
in an indicator bacterial strain, The results show that double psoral
en adducts, located at both ends of a long triple helix, cannot be rep
aired efficiently in human cells.