Bias in Nucleotide Composition of Antisense Oligonucleotides
Authors:
- Toon F.C.M. SmetsersTSToon F.C.M. Smetsers
- Jan B.M. BoezemanJBJan B.M. Boezeman
- Ewald J.B.M. MensinkEMEwald J.B.M. Mensink
- 1 January 1996
- journal article
- research article
- Published by SAGE Publications in Antisense and Nucleic Acid Drug Development
- Vol. 6 (1) , 63-67
Abstract
In this study we investigated if specific sequence motifs occur with a higher frequency in antisense oligonucleotides than can be expected on the basis of the mRNA composition to get an impression of the importance of these motifs for antisense effects. Computer analysis of 206 antisense oligonucleotides extracted from the literature and from sequence databases, all targeted against human mRNA, was performed. We compared the sequence composition of these oligonucleotides with the average of 100 equally large and randomly selected sequences from sequence databases and of their target mRNA. We found that the frequency of sequence motifs containing GG, CCC, CC, GAC, and CG is significantly higher and TT and that TCC is significantly lower in antisense oligonucleotide sequences than in the randomly selected mRNA sequences. We conclude that there is a bias in the nucleotide composition of antisense oligonucleotides. Some of these biased sequence motifs have been reported to induce nonantisense effects mediated by protein binding. Further analysis of the biologic function of these motifs is necessary to investigate if they should be avoided or incorporated into future designs of therapeutic effective oligonucleotides.Keywords
This publication has 4 references indexed in Scilit:
- Antisense oligonucleotides directed against p53 have antiproliferative effects unrelated to effects on p53 expressionBritish Journal of Cancer, 1995
- Inhibition of Protein-Tyrosine Kinase Activity in Intact Cells by the Aptameric Action of OligodeoxynucleotidesAntisense Research and Development, 1995
- Aptameric inhibition of p210bcr-abltyrosine kinase autophosphorylation by oligodeoxynucleotides of defined sequence and backbone structureNucleic Acids Research, 1994
- Sequence specific inhibition of human type II phospholipase A2, enzyme activity by phosphorothioate oligonucleotidesNucleic Acids Research, 1994