The novel double-folded structure of d(GCATGCATGC): a possible model for triplet-repeat sequences.

Arunachalam Thirugnanasambandam, Selvam Karthik, Pradeep Kumar Mandal, Namasivayam Gautham
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引用次数: 3

Abstract

The structure of the decadeoxyribonucleotide d(GCATGCATGC) is presented at a resolution of 1.8 Å. The decamer adopts a novel double-folded structure in which the direction of progression of the backbone changes at the two thymine residues. Intra-strand stacking interactions (including an interaction between the endocylic O atom of a ribose moiety and the adjacent purine base), hydrogen bonds and cobalt-ion interactions stabilize the double-folded structure of the single strand. Two such double-folded strands come together in the crystal to form a dimer. Inter-strand Watson-Crick hydrogen bonds form four base pairs. This portion of the decamer structure is similar to that observed in other previously reported oligonucleotide structures and has been dubbed a `bi-loop'. Both the double-folded single-strand structure, as well as the dimeric bi-loop structure, serve as starting points to construct models for triplet-repeat DNA sequences, which have been implicated in many human diseases.

新的双折叠结构d(GCATGCATGC):三重重复序列的可能模型。
十氧核糖核苷酸d(GCATGCATGC)的结构以1.8的分辨率表示Å。该十聚体采用一种新颖的双折叠结构,在这种结构中,主链的进展方向在两个胸腺嘧啶残基处发生了变化。链内堆叠相互作用(包括核糖片段的内环O原子与邻近嘌呤碱基之间的相互作用)、氢键和钴离子相互作用稳定了单链的双折叠结构。两个这样的双折叠链在晶体中聚集在一起形成二聚体。跨链沃森-克里克氢键形成四个碱基对。十聚体结构的这一部分与先前报道的其他寡核苷酸结构相似,被称为“双环”。双折叠单链结构和二聚体双环结构都是构建与许多人类疾病有关的三重重复DNA序列模型的起点。
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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