In this study, we report the first atomic resolution structure of a stable G-hairpin formed by a natively occurring DNA sequence. An 11-nt long G-rich DNA oligonucleotide, 5'-d(GTGTGGGTGTG)-3', corresponding to the most abundant sequence motif in irregular telomeric DNA from Saccharomyces cerevisiae (yeast), is demonstrated to adopt a novel type of mixed parallel/antiparallel fold-back DNA structure, which is stabilized by dynamic G:G base pairs that transit between N1-carbonyl symmetric and N1-carbonyl, N7-amino base-pairing arrangements. Although the studied sequence first appears to possess a low capacity for base pairing, it forms a thermodynamically stable structure with a rather complex topology that includes a chain reversal arrangement of the backbone in the center of the continuous G-tract and 3'-to-5' stacking of the terminal residues. The structure reveals previously unknown principles of the folding of G-rich oligonucleotides that could be applied to the prediction of natural and/or the design of artificial recognition DNA elements. The structure also demonstrates that the folding landscapes of short DNA single strands is much more complex than previously assumed.

Structure of a Stable G-Hairpin / Gajarský, Martin; Živković, Martina Lenarčič; Stadlbauer, Petr; Pagano, Bruno; Fiala, Radovan; Amato, Jussara; Tomáška, L'Ubomír; Šponer, Jiří; Plavec, Janez; Trantírek, Lukáš. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 139:10(2017), pp. 3591-3594. [10.1021/jacs.6b10786]

Structure of a Stable G-Hairpin

PAGANO, BRUNO;AMATO, JUSSARA;
2017

Abstract

In this study, we report the first atomic resolution structure of a stable G-hairpin formed by a natively occurring DNA sequence. An 11-nt long G-rich DNA oligonucleotide, 5'-d(GTGTGGGTGTG)-3', corresponding to the most abundant sequence motif in irregular telomeric DNA from Saccharomyces cerevisiae (yeast), is demonstrated to adopt a novel type of mixed parallel/antiparallel fold-back DNA structure, which is stabilized by dynamic G:G base pairs that transit between N1-carbonyl symmetric and N1-carbonyl, N7-amino base-pairing arrangements. Although the studied sequence first appears to possess a low capacity for base pairing, it forms a thermodynamically stable structure with a rather complex topology that includes a chain reversal arrangement of the backbone in the center of the continuous G-tract and 3'-to-5' stacking of the terminal residues. The structure reveals previously unknown principles of the folding of G-rich oligonucleotides that could be applied to the prediction of natural and/or the design of artificial recognition DNA elements. The structure also demonstrates that the folding landscapes of short DNA single strands is much more complex than previously assumed.
2017
Structure of a Stable G-Hairpin / Gajarský, Martin; Živković, Martina Lenarčič; Stadlbauer, Petr; Pagano, Bruno; Fiala, Radovan; Amato, Jussara; Tomáška, L'Ubomír; Šponer, Jiří; Plavec, Janez; Trantírek, Lukáš. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 139:10(2017), pp. 3591-3594. [10.1021/jacs.6b10786]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/667688
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