Abstract

Stable DNA loop structures closed by a novel G·C base-pair have been determined for the single-residue d(G XC) loops ( X=A, T, G or C) in low-salt solution by high-resolution nuclear magnetic resonance (NMR) techniques. The closing G·C base-pair in these loops is not of the canonical Watson–Crick type, but adopts instead a unique sheared-type ( trans Watson–Crick/sugar-edge) pairing, like those occurring in the sheared mismatched G·A or A·C base-pair, to draw the two opposite strands together. The cytidine residue in the closing base-pair is transformed into the rare syn domain to form two H-bonds with the guanine base and to prevent the steric clash between the G 2NH 2 and the C H-5 protons. Besides, the sugar pucker of the syn cytidine is still located in the regular C2′- endo domain, unlike the C3′- endo domain adopted for the pyrimidines of the out-of-alternation left-handed Z-DNA structure. The facile formation of the compact d(G XC) loops closed by a unique sheared-type G anti ·C syn base-pair demonstrates the great potential of the single-stranded d(G XC) triplet repeats to fold into stable hairpins.

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