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G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition
Chromosomes in vertebrates are protected at both ends by telomere DNA composed of tandem (TTAGGG)(n) repeats. DNA replication produces a blunt-ended leading strand telomere and a lagging strand telomere carrying a single-stranded G-rich overhang at its end. The G-rich strand can form G-quadruplex st...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1920240/ https://www.ncbi.nlm.nih.gov/pubmed/17488850 http://dx.doi.org/10.1093/nar/gkm203 |
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author | Kan, Zhong-yuan Lin, Yi Wang, Feng Zhuang, Xin-ying Zhao, Yong Pang, Dai-wen Hao, Yu-hua Tan, Zheng |
author_facet | Kan, Zhong-yuan Lin, Yi Wang, Feng Zhuang, Xin-ying Zhao, Yong Pang, Dai-wen Hao, Yu-hua Tan, Zheng |
author_sort | Kan, Zhong-yuan |
collection | PubMed |
description | Chromosomes in vertebrates are protected at both ends by telomere DNA composed of tandem (TTAGGG)(n) repeats. DNA replication produces a blunt-ended leading strand telomere and a lagging strand telomere carrying a single-stranded G-rich overhang at its end. The G-rich strand can form G-quadruplex structure in the presence of K(+) or Na(+). At present, it is not clear whether quadruplex can form in the double-stranded telomere region where the two complementary strands are constrained in close vicinity and quadruplex formation, if possible, has to compete with the formation of the conventional Watson–Crick duplex. In this work, we studied quadruplex formation in oligonucleotides and double-stranded DNA containing both the G- and C-rich sequences to better mimic the in vivo situation. Under such competitive condition only duplex was observed in dilute solution containing physiological concentration of K(+). However, quadruplex could preferentially form and dominate over duplex structure under molecular crowding condition created by PEG as a result of significant quadruplex stabilization and duplex destabilization. This observation suggests quadruplex may potentially form or be induced at the blunt end of a telomere, which may present a possible alternative form of structures at telomere ends. |
format | Text |
id | pubmed-1920240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-19202402007-07-19 G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition Kan, Zhong-yuan Lin, Yi Wang, Feng Zhuang, Xin-ying Zhao, Yong Pang, Dai-wen Hao, Yu-hua Tan, Zheng Nucleic Acids Res Structural Biology Chromosomes in vertebrates are protected at both ends by telomere DNA composed of tandem (TTAGGG)(n) repeats. DNA replication produces a blunt-ended leading strand telomere and a lagging strand telomere carrying a single-stranded G-rich overhang at its end. The G-rich strand can form G-quadruplex structure in the presence of K(+) or Na(+). At present, it is not clear whether quadruplex can form in the double-stranded telomere region where the two complementary strands are constrained in close vicinity and quadruplex formation, if possible, has to compete with the formation of the conventional Watson–Crick duplex. In this work, we studied quadruplex formation in oligonucleotides and double-stranded DNA containing both the G- and C-rich sequences to better mimic the in vivo situation. Under such competitive condition only duplex was observed in dilute solution containing physiological concentration of K(+). However, quadruplex could preferentially form and dominate over duplex structure under molecular crowding condition created by PEG as a result of significant quadruplex stabilization and duplex destabilization. This observation suggests quadruplex may potentially form or be induced at the blunt end of a telomere, which may present a possible alternative form of structures at telomere ends. Oxford University Press 2007-06 2007-05-08 /pmc/articles/PMC1920240/ /pubmed/17488850 http://dx.doi.org/10.1093/nar/gkm203 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Kan, Zhong-yuan Lin, Yi Wang, Feng Zhuang, Xin-ying Zhao, Yong Pang, Dai-wen Hao, Yu-hua Tan, Zheng G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title | G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title_full | G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title_fullStr | G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title_full_unstemmed | G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title_short | G-quadruplex formation in human telomeric (TTAGGG)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
title_sort | g-quadruplex formation in human telomeric (ttaggg)(4) sequence with complementary strand in close vicinity under molecularly crowded condition |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1920240/ https://www.ncbi.nlm.nih.gov/pubmed/17488850 http://dx.doi.org/10.1093/nar/gkm203 |
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