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The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics

A telomere carrying repetitive sequences ends with a single-stranded overhang. The G-rich overhang could fold back and bind in the major groove of its upstream duplex, forming an antiparallel triplex structure. The telomeric triplex has been proposed to function in protecting chromosome ends. Howeve...

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Autores principales: Li, Ning, Wang, Junli, Ma, Kangkang, Liang, Lin, Mi, Lipei, Huang, Wei, Ma, Xiaofeng, Wang, Zeyu, Zheng, Wei, Xu, Linyan, Chen, Jun-Hu, Yu, Zhongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735771/
https://www.ncbi.nlm.nih.gov/pubmed/31114915
http://dx.doi.org/10.1093/nar/gkz464
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author Li, Ning
Wang, Junli
Ma, Kangkang
Liang, Lin
Mi, Lipei
Huang, Wei
Ma, Xiaofeng
Wang, Zeyu
Zheng, Wei
Xu, Linyan
Chen, Jun-Hu
Yu, Zhongbo
author_facet Li, Ning
Wang, Junli
Ma, Kangkang
Liang, Lin
Mi, Lipei
Huang, Wei
Ma, Xiaofeng
Wang, Zeyu
Zheng, Wei
Xu, Linyan
Chen, Jun-Hu
Yu, Zhongbo
author_sort Li, Ning
collection PubMed
description A telomere carrying repetitive sequences ends with a single-stranded overhang. The G-rich overhang could fold back and bind in the major groove of its upstream duplex, forming an antiparallel triplex structure. The telomeric triplex has been proposed to function in protecting chromosome ends. However, we lack strategies to mechanically probe the dynamics of a telomeric triplex. Here, we show that the topological dynamics of a telomeric triplex involves 3′ overhang binding at the ds/ssDNA junction inferred by DNA mechanics. Assisted by click chemistry and branched polymerase chain reaction, we developed a rescue-rope-strategy for mechanically manipulating an artificial telomeric DNA with a free end. Using single-molecule magnetic tweezers, we identified a rarely forming (5%) telomeric triplex which pauses at an intermediate state upon unzipping the Watson–Crick paired duplex. Our findings revealed that a mechanically stable triplex formed in a telomeric DNA can resist a force of 20 pN for a few seconds in a physiological buffer. We also demonstrated that the rescue-rope-strategy assisted mechanical manipulation can directly rupture the interactions between the third strand and its targeting duplex in a DNA triplex. Our single-molecule rescue-rope-strategy will serve as a general tool to investigate telomere dynamics and further develop triplex-based biotechnologies.
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spelling pubmed-67357712019-09-16 The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics Li, Ning Wang, Junli Ma, Kangkang Liang, Lin Mi, Lipei Huang, Wei Ma, Xiaofeng Wang, Zeyu Zheng, Wei Xu, Linyan Chen, Jun-Hu Yu, Zhongbo Nucleic Acids Res Methods Online A telomere carrying repetitive sequences ends with a single-stranded overhang. The G-rich overhang could fold back and bind in the major groove of its upstream duplex, forming an antiparallel triplex structure. The telomeric triplex has been proposed to function in protecting chromosome ends. However, we lack strategies to mechanically probe the dynamics of a telomeric triplex. Here, we show that the topological dynamics of a telomeric triplex involves 3′ overhang binding at the ds/ssDNA junction inferred by DNA mechanics. Assisted by click chemistry and branched polymerase chain reaction, we developed a rescue-rope-strategy for mechanically manipulating an artificial telomeric DNA with a free end. Using single-molecule magnetic tweezers, we identified a rarely forming (5%) telomeric triplex which pauses at an intermediate state upon unzipping the Watson–Crick paired duplex. Our findings revealed that a mechanically stable triplex formed in a telomeric DNA can resist a force of 20 pN for a few seconds in a physiological buffer. We also demonstrated that the rescue-rope-strategy assisted mechanical manipulation can directly rupture the interactions between the third strand and its targeting duplex in a DNA triplex. Our single-molecule rescue-rope-strategy will serve as a general tool to investigate telomere dynamics and further develop triplex-based biotechnologies. Oxford University Press 2019-09-05 2019-05-22 /pmc/articles/PMC6735771/ /pubmed/31114915 http://dx.doi.org/10.1093/nar/gkz464 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Li, Ning
Wang, Junli
Ma, Kangkang
Liang, Lin
Mi, Lipei
Huang, Wei
Ma, Xiaofeng
Wang, Zeyu
Zheng, Wei
Xu, Linyan
Chen, Jun-Hu
Yu, Zhongbo
The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title_full The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title_fullStr The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title_full_unstemmed The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title_short The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics
title_sort dynamics of forming a triplex in an artificial telomere inferred by dna mechanics
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735771/
https://www.ncbi.nlm.nih.gov/pubmed/31114915
http://dx.doi.org/10.1093/nar/gkz464
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