In order to identify the optimal target sites for antisense oligonucleotide
s in the human multiple drug resistance mRNA, the secondary structure of th
e 5'-terminal part of this mRNA (nucleotides 1-678) was investigated. By us
ing results of probing with ribonucleases T1, ONE and V1 and results of com
puter simulations, a model of the 5'-region of the PGY1/MDR1 mRNA wits buil
t. The molecule is formed by three major domains comprising several hairpin
s separated by single-stranded fragments. The predicted single-stranded reg
ions of the PGY1/MDR1 mRNA efficiently bind complementary oligonucleotides,
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