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在K溶液中由人端粒变异DNA形成的椅型G-四链体结构。

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

作者信息

Liu Changdong, Zhou Bo, Geng Yanyan, Yan Tam Dick, Feng Rui, Miao Haitao, Xu Naining, Shi Xiao, You Yingying, Hong Yuning, Tang Ben Zhong, Kwan Lo Pik, Kuryavyi Vitaly, Zhu Guang

机构信息

Division of Life Science , The Hong Kong University of Science and Technology , Clear Water Bay , Kowloon , Hong Kong SAR , China . Email:

Institute for Advanced Study , The Hong Kong University of Science and Technology , Clear Water Bay , Kowloon , Hong Kong SAR , China.

出版信息

Chem Sci. 2018 Oct 4;10(1):218-226. doi: 10.1039/c8sc03813a. eCollection 2019 Jan 7.

DOI:10.1039/c8sc03813a
PMID:30713633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6330691/
Abstract

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], T. 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 T 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·T18 base pair. The loops are edgewise; glycosidic conformation of guanines is ··· around each tetrad, 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.

摘要

已知人类端粒DNA序列中的鸟嘌呤链可折叠成八种不同的四链结构,这些结构因鸟嘌呤核苷酸在其核心G-四联体堆叠中的构象以及连接环的不同种类和顺序而异,这些连接环被称为G-四链体。在此,我们展示了一种由人类端粒变体d[(GGGTTA)2GGGTTTGGG],即T,在K溶液中形成的新型G-四链体结构。这种变体DNA位于人类染色体8、11、17和19的亚端粒区域,以及5号染色体的DNase超敏区域和着丝粒下区域。有趣的是,使T与人类端粒序列不同的单个A18T替换导致形成了一种三层椅型G-四链体,这是一种在人类端粒重复序列中以前未知的折叠形式,有两个环通过反向沃森-克里克A6·T18碱基对相互作用。这些环是边缘排列的;鸟嘌呤的糖苷构象在每个四联体周围是···,核心的每条链有两条反平行的相邻链。我们的结果扩展了已知的G-四链体折叠拓扑结构库,并可能为基于结构的抗癌药物设计提供潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/47f19c373c48/c8sc03813a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/1cdac07be806/c8sc03813a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/c9cbc6b1b2a4/c8sc03813a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/4c1e2c235ae7/c8sc03813a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/0131906627fb/c8sc03813a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/2a6eb035fde3/c8sc03813a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/47f19c373c48/c8sc03813a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/1cdac07be806/c8sc03813a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/c9cbc6b1b2a4/c8sc03813a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/4c1e2c235ae7/c8sc03813a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/0131906627fb/c8sc03813a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/2a6eb035fde3/c8sc03813a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dc/6330691/47f19c373c48/c8sc03813a-f6.jpg

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