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Solution structures of the individual single strands of the fragile X DNA triplets (GCC)n.(GGC)n.

机译:易碎X DNA三胞胎(GCC)n。(GGC)n的单个单链的溶液结构。

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摘要

Three-dimensional structures of the fragile X triplet repeats (GCC)n and (GGC)n are derived by using one- dimensional/two-dimensional NMR. Under a wide range of solution conditions (10-150 mM NaCl,pH6-7)(GCC)5-7 strands form exclusively slipped hairpins with a 3' overhanging C. The slipped hairpins of (GCC)n strands show the following structural characteristics: (i) maximization of Watson-Crick G.C pairs; (ii) formation of C.C mispairs at the CpG steps in the stem; (iii) C2'-endo, anti conformations for all the nucleotides. The ability of (GCC)n strands to form hairpin structures more readily than complementary (GGC)n strands suggests preferential slippage during replication and subsequent expansion of the (GCC)n strands. In addition, the C.C. mispairs at the CpG site of (GCC)n hairpins account for their exceptional substrate efficiencies for human methyltransferase. Gel electrophoresis data show that (GGC)n strands form both hairpin and mismatched duplex structures in 10-150 mM NaCl (ph 6-7) for n < 10, but for n > or + 11 hairpin structures are exclusively present. However, (GGC)n strands remain predominantly in the duplex state for n=4-11 under NMR solution conditions, which require DNA concentrations 100- to 1000-fold higher than in gel electrophoresis. NMR analyses of [(GGC)n]2 duplexes for n=4-6 show the presence of Watson-Crick G.C and mismatched G anti G syn pairs. The mismatches adjacent to the CpG step introduce local structural flexibility in these duplexes. Similar structural properties are also expected in the stem of the hairpins formed by (GGC)n strands.
机译:通过使用一维/二维NMR,获得了脆弱的X三重态重复​​(GCC)n和(GGC)n的三维结构。在各种溶液条件下(10-150 mM NaCl,pH6-7)(GCC)5-7链仅形成带有3'突出C的滑动发夹。(GCC)n链的滑动发夹显示以下结构特征:(i)最大化Watson-Crick GC对; (ii)在茎的CpG步骤形成C.C错配; (iii)所有核苷酸的C2'-内切,反构象。 (GCC)n链比互补的(GGC)n链更容易形成发夹结构的能力表明,在(GCC)n链的复制和随后的扩增过程中,存在优先的滑动。此外,抄送(GCC)n发夹的CpG位点的错配说明了它们对人甲基转移酶的出色底物效率。凝胶电泳数据显示(GGC)n链同时在10-150 mM NaCl(ph 6-7)中形成发夹和错配的双链结构,其中n <10,但n>或+ 11时仅存在发夹结构。但是,(GGC)n链在NMR溶液条件下主要保持双链状态,n = 4-11,这要求DNA浓度比凝胶电泳高100-1000倍。 [(GGC)n] 2双链体的NMR分析,n = 4-6,表明存在Watson-Crick G.C和错配的G反G syn对。与CpG步骤相邻的错配在这些双链体中引入了局部结构灵活性。由(GGC)n链形成的发夹的茎中也预期有类似的结构特性。

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