Structure of a human telomeric DNA sequence stabilized by 8-bromoguanosine substitutions, as determined by NMR in a K+ solution

被引:79
作者
Matsugami, Akimasa
Xu, Yan
Noguchi, Yuuki
Sugiyama, Hiroshi
Katahira, Masato
机构
[1] Yokohama City Univ, Int Grad Sch Arts & Sci, Tsurumi Ku, Yokohama, Kanagawa 230045, Japan
[2] Kyoto Univ, Grad Sch Sci, Kyoto, Japan
[3] RIKEN, Yokohama, Kanagawa, Japan
[4] PRESTO, Yokohama, Kanagawa, Japan
关键词
8-bromoguanosine; NMR; quadruplex; structure; telomere;
D O I
10.1111/j.1742-4658.2007.05881.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structure of human telomeric DNA is controversial; it depends upon the sequence contexts and the methodologies used to determine it. The solution structure in the presence of K+ is particularly interesting, but the structure is yet to be elucidated, due to possible conformational heterogeneity. Here, a unique strategy is applied to stabilize one such structure in a K+ solution by substituting guanosines with 8-bromoguanosines at proper positions. The resulting spectra are cleaner and led to determination of the structure at a high atomic resolution. This demonstrates that the application of 8-bromoguanosine is a powerful tool to overcome the difficulty of nucleic acid structure determination arising from conformational heterogeneity. The obtained structure is a mixed-parallel/antiparallel quadruplex. The structure of telomeric DNA was recently reported in another study, in which stabilization was brought about by mutation and resultant additional interactions [Luu KN, Phan AT, Kuryavyi V, Lacroix L & Patel DJ (2006) Structure of the human telomere in K+ solution: an intramolecular (3+1) G-quadruplex scaffold. J Am Chem Soc 128, 9963-9970]. The structure of the guanine tracts was similar between the two. However, a difference was seen for loops connecting guanine tracts, which may play a role in the higher order arrangement of telomeres. Our structure can be utilized to design a small molecule which stabilizes the quadruplex. This type of molecule is supposed to inhibit a telomerase and thus is expected to be a candidate anticancer drug.
引用
收藏
页码:3545 / 3556
页数:12
相关论文
共 43 条
[31]   DETERMINATION OF THE DNA SUGAR PUCKER USING C-13 NMR-SPECTROSCOPY [J].
SANTOS, RA ;
TANG, P ;
HARBISON, GS .
BIOCHEMISTRY, 1989, 28 (24) :9372-9378
[32]   Design and synthesis of an expanded porphyrin that has selectivity for the c-MYC G-quadruplex structure [J].
Seenisamy, J ;
Bashyam, S ;
Gokhale, V ;
Vankayalapati, H ;
Sun, D ;
Siddiqui-Jain, A ;
Streiner, N ;
Shin-ya, K ;
White, E ;
Wilson, WD ;
Hurley, LH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (09) :2944-2959
[33]   Phosphorothioate substitution can substantially alter RNA conformation [J].
Smith, JS ;
Nikonowicz, EP .
BIOCHEMISTRY, 2000, 39 (19) :5642-5652
[34]   Method for direct discrimination of intra- and intermolecular hydrogen bonds, and characterization of the G(:A):G(:A):G(:A):G heptad, with scalar couplings across hydrogen bonds [J].
Sotoya, H ;
Matsugami, A ;
Ikeda, T ;
Ouhashi, K ;
Uesugi, S ;
Katahira, M .
NUCLEIC ACIDS RESEARCH, 2004, 32 (17) :5113-5118
[35]   TRF2 protects human telomeres from end-to-end fusions [J].
van Steensel, B ;
Smogorzewska, A ;
de Lange, T .
CELL, 1998, 92 (03) :401-413
[36]   NMR investigation of RNA structure [J].
Varani, G ;
Aboulela, F ;
Allain, FHT .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 1996, 29 :51-127
[37]   SOLUTION STRUCTURE OF THE HUMAN TELOMERIC REPEAT D[AG(3)(T(2)AG(3))3] G-TETRAPLEX [J].
WANG, Y ;
PATEL, DJ .
STRUCTURE, 1993, 1 (04) :263-282
[38]   SOLUTION STRUCTURE OF THE TETRAHYMENA TELOMERIC REPEAT D(T(2)G(4))(4) G-TETRAPLEX [J].
WANG, Y ;
PATEL, DJ .
STRUCTURE, 1994, 2 (12) :1141-1156
[39]   The new models of the human telomere d[AGGG(TTAGGG)3] in K+ solution [J].
Xu, Yan ;
Noguchi, Yuki ;
Sugiyama, Hiroshi .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (16) :5584-5591
[40]   Characterization of structure and stability of long telomeric DNA G-quadruplexes [J].
Yu, Hai-Qing ;
Miyoshi, Daisuke ;
Sugimoto, Naoki .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (48) :15461-15468