Abstract
Alternate-strand triple helix formation was optimized at the two junction steps, the 5'-TpA-3' and 5'-ApT-3' junctions. Footprint experiments, gel retardation assays and thermal denaturation measures on a sequence appropriately designed with two adjacent alternate-strand polypurine tracts points out that the addition of an adenine residue and the removal of one nucleotide should facilitate the crossing strands at the 5'-TpA-3' junction and at the 5'-ApT-3' junction, respectively. These results provide a 'switch code' for the construction of alternate-strand triple helix forming oligonucleotides which open new possibilities for extending the range of applications of antigene strategy.
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CITATION STYLE
Brodin, P., Sun, J. S., Mouscadet, J. F., & Auclair, C. (1999). Optimization of alternate-strand triple helix formation at the 5’-TpA-3’ and 5’-ApT-3’ junctions. Nucleic Acids Research, 27(15), 3029–3034. https://doi.org/10.1093/nar/27.15.3029
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