A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K+ solution

被引:46
|
作者
Liu, Changdong [1 ]
Zhou, Bo [1 ,2 ]
Geng, Yanyan [1 ]
Tam, Dick Yan [3 ]
Feng, Rui [1 ]
Miao, Haitao [1 ]
Xu, Naining [1 ]
Shi, Xiao [1 ]
You, Yingying [1 ]
Hong, Yuning [4 ]
Tang, Ben Zhong [4 ]
Lo, Pik Kwan [3 ]
Kuryavyi, Vitaly [5 ]
Zhu, Guang [1 ,6 ,7 ]
机构
[1] Hong Kong Univ Sci & Technol, Div Life Sci, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Inst Adv Study, Clear Water Bay, Kowloon, Hong Kong, Peoples R China
[3] City Univ Hong Kong, Dept Biol & Chem, Kowloon Tong, 83 Tat Chee Ave, Hong Kong, Peoples R China
[4] Hong Kong Univ Sci & Technol, Dept Chem, Clear Water Bay, Kowloon, Hong Kong, Peoples R China
[5] Mem Sloan Kettering Canc Ctr, Struct Biol Program, 1275 York Ave, New York, NY 10021 USA
[6] Hong Kong Univ Sci & Technol, Inst Adv Study, Clear Water Bay, Kowloon, Hong Kong, Peoples R China
[7] Hong Kong Univ Sci & Technol, State Key Lab Mol Neurosci, Clear Water Bay, Kowloon, Hong Kong, Peoples R China
关键词
GEOMETRIC PARAMETERS; CIRCULAR-DICHROISM; TOPOLOGY; SEQUENCE; TARGET; ANGLE; ALS;
D O I
10.1039/c8sc03813a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Guanine tracts of human telomeric DNA sequences are known to fold into eight different four-stranded structures that vary by the conformation of guanine nucleotides arranged in the stack of G-tetrads in their core and by different kinds and orders of connecting loops, called G-quadruplexes. Here, we present a novel G-quadruplex structure formed in K+ solution by a human telomeric variant d[(GGGTTA)2GGGTTTGGG], htel21T(18). This variant DNA is located in the subtelomeric regions of human chromosomes 8, 11, 17, and 19 as well as in the DNase hypersensitive region and in the subcentromeric region of chromosome 5. Interestingly, single A18T substitution that makes htel21T(18) different from the human telomeric sequence results in the formation of a three-layer chair-type G-quadruplex, a fold previously unknown among human telomeric repeats, with two loops interacting through the reverse Watson-Crick A6<bold>T</bold>18 base pair. The loops are edgewise; glycosidic conformation of guanines is syn<bold>antisynanti around each tetrad</bold>, and each strand of the core has two antiparallel adjacent strands. Our results expand the repertoire of known G-quadruplex folding topologies and may provide a potential target for structure-based anticancer drug design.
引用
收藏
页码:218 / 226
页数:9
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