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

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330691/
https://www.ncbi.nlm.nih.gov/pubmed/30713633
http://dx.doi.org/10.1039/c8sc03813a
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author 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
author_facet 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
author_sort Liu, Changdong
collection PubMed
description 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·T18 base pair. The loops are edgewise; glycosidic conformation of guanines is syn·anti·syn·anti 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.
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spelling pubmed-63306912019-02-01 A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution 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 Chem Sci Chemistry 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·T18 base pair. The loops are edgewise; glycosidic conformation of guanines is syn·anti·syn·anti 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. Royal Society of Chemistry 2018-10-04 /pmc/articles/PMC6330691/ /pubmed/30713633 http://dx.doi.org/10.1039/c8sc03813a Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
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
A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title_full A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title_fullStr A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title_full_unstemmed A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title_short A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
title_sort chair-type g-quadruplex structure formed by a human telomeric variant dna in k(+) solution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330691/
https://www.ncbi.nlm.nih.gov/pubmed/30713633
http://dx.doi.org/10.1039/c8sc03813a
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