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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-6330691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
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title_fullStr | A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
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title_full_unstemmed | A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
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title_short | A chair-type G-quadruplex structure formed by a human telomeric variant DNA in K(+) solution
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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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