Kettani A, Bouaziz S, Gorin A, Zhao H, Jones R A, Patel D J
Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York, NY, 10021, USA.
J Mol Biol. 1998 Sep 25;282(3):619-36. doi: 10.1006/jmbi.1998.2030.
We have applied NMR and molecular dynamics computations including intensity based refinement to define the structure of the d(G-G-G-C-T4-G-G-G-C) dodecanucleotide in 100 mM NaCl solution. The G-G-G-C sequence is of interest since it has been found as tandem repeats in the DNA sequence of human chromosome 19. The same G-G-G-C sequence is also seen as islands in adeno-associated virus, a human parvovirus, which is unique amongst eukaryotic DNA viruses in its ability to integrate site-specifically into a defined region of human chromosome 19. The d(G-G-G-C-T4-G-G-G-C) sequence forms a quadruplex in Na cation containing solution through head-to-tail dimerization of two symmetry-related stem-hairpin loops with adjacent strands antiparallel to each other around the quadruplex. The connecting T4 loops are of the lateral type, resulting in a quadruplex structure containing two internal G.G.G.G tetrads flanked by G.C.G.C tetrads. The G(anti).G(syn).G(anti).G(syn) tetrads are formed through dimerization associated hydrogen bonding alignments of a pair of Hoogsteen G(anti).G(syn) mismatch pairs, while the G(anti).C(anti).G(anti).C(anti) tetrads are formed through dimerization associated bifurcated hydrogen bonding alignments involving the major groove edges of a pair of Watson-Crick G.C base-pairs. The quadruplex contains two distinct narrow and two symmetric wide grooves with extensive stacking between adjacent tetrad planes. The structure of the quadruplex contains internal cavities that can potentially accommodate Na cations positioned between adjacent tetrad planes. Three such Na cations have been modeled into the structure of the d(G-G-G-C-T4-G-G-G-C) quadruplex. Finally, we speculate on the potential role of quadruplex formation involving G.G.G.G and G.C.G.C tetrads during the integration of the adeno-associated parvovirus into its target on human chromosome 19, both of which involve stretches of G-G-G-C sequence elements.
我们应用了核磁共振(NMR)和分子动力学计算,包括基于强度的精修,以确定100 mM NaCl溶液中十二聚体d(G-G-G-C-T4-G-G-G-C)的结构。G-G-G-C序列备受关注,因为它在人类19号染色体的DNA序列中被发现为串联重复序列。相同的G-G-G-C序列在腺相关病毒(一种人类细小病毒)中也被视为岛状结构,腺相关病毒在真核DNA病毒中独一无二,能够位点特异性地整合到人类19号染色体的特定区域。d(G-G-G-C-T4-G-G-G-C)序列在含Na阳离子的溶液中通过两个对称相关的茎环的头对头二聚化形成四链体,相邻链在四链体周围相互反平行。连接的T4环为侧向型,形成一个包含两个内部G.G.G.G四分体且两侧为G.C.G.C四分体的四链体结构。G(反式).G(顺式).G(反式).G(顺式)四分体通过一对Hoogsteen G(反式).G(顺式)错配配对的二聚化相关氢键排列形成,而G(反式).C(反式).G(反式).C(反式)四分体通过涉及一对沃森-克里克G.C碱基对大沟边缘的二聚化相关分叉氢键排列形成。该四链体包含两个不同的窄沟和两个对称的宽沟,相邻四分体平面之间有广泛的堆积。四链体的结构包含内部空腔,这些空腔可能容纳位于相邻四分体平面之间的Na阳离子。三个这样的Na阳离子已被模拟到d(G-G-G-C-T4-G-G-G-C)四链体的结构中。最后,我们推测在腺相关细小病毒整合到人类19号染色体上的靶位点过程中,涉及G.G.G.G和G.C.G.C四分体的四链体形成的潜在作用,这两者都涉及连续的G-G-G-C序列元件。