X-ray structure of d(GCGAAGC); switching of partner for G:A pair in duplex form.

T. Sunami, J. Kondo, M. Tsunoda, T. Sekiguchi, I. Hirao, Kimitsuna Watanabe, K. Miura, A. Takénaka
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Abstract

Crystal structure of a DNA fragment d(GCGAAGC), known to adopt a stable mini-hairpin structure in solution, has been determined at 1.6A resolution. Two heptamers are associated to form a duplex with a molecular two-fold symmetry. Three duplexes in the asymmetric unit have a similar structure. At the both ends of each duplexes, two Watson-Crick G:C pairs constitute the stem region. In the central part, two sheared pairs of G:A and A:G are formed, the two G bases being stacked as well as the two A bases. At this point, the two strands are crossed between the two base-stacked columns. The adenine moiety of the bulged A5 residue, which intercalates between the A4 and G6 residues, makes a small bending of the duplex at the two sites. The difference between the bulge-in structure of d(GCGAAGC) and the zipper-like duplex of d(GCGAAAGC) is ascribed to switching the partner of the sheared G:A pairs.
d(GCGAAGC)的x射线结构G的交换伙伴:双工形式的一对。
以1.6A的分辨率测定了DNA片段d(GCGAAGC)在溶液中呈稳定的微型发夹结构的晶体结构。两个七聚体结合形成具有分子双重对称的双聚体。不对称单元中的三个双链具有相似的结构。在每个双链的两端,两个沃森-克里克G:C对构成茎区。在中心部分,形成两对剪切的G:A和A:G,两个G碱基堆叠,两个A碱基堆叠。在这一点上,两条线在两个基础堆叠的柱子之间交叉。凸起的A5残基的腺嘌呤部分插入到A4和G6残基之间,使两个位点的双链发生小的弯曲。d的凸起结构(GCGAAGC)与d的拉链状双工结构(GCGAAAGC)之间的差异是由于剪切G:A对的对偶体发生了交换。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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