DNA Quadruplex Structure with a Unique Cation Dependency
DNA quadruplex structures provide an additional layer of regulatory control in genome maintenance and gene expression and are widely used in nanotechnology. We report the discovery of an unprecedented tetrastranded structure formed from a native G‐rich DNA sequence originating from the telomeric reg...
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Veröffentlicht in: | Angewandte Chemie 2024-02, Vol.136 (7), p.n/a |
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creator | Gajarsky, Martin Stadlbauer, Petr Sponer, Jiri Cucchiarini, Anne Dobrovolna, Michaela Brazda, Vaclav Mergny, Jean‐Louis Trantirek, Lukas Lenarcic Zivkovic, Martina |
description | DNA quadruplex structures provide an additional layer of regulatory control in genome maintenance and gene expression and are widely used in nanotechnology. We report the discovery of an unprecedented tetrastranded structure formed from a native G‐rich DNA sequence originating from the telomeric region of Caenorhabditis elegans. The structure is defined by multiple properties that distinguish it from all other known DNA quadruplexes. Most notably, the formation of a stable so‐called KNa‐quadruplex (KNaQ) requires concurrent coordination of K+ and Na+ ions at two distinct binding sites. This structure provides novel insight into G‐rich DNA folding under ionic conditions relevant to eukaryotic cell physiology and the structural evolution of telomeric DNA. It highlights the differences between the structural organization of human and nematode telomeric DNA, which should be considered when using C. elegans as a model in telomere biology, particularly in drug screening applications. Additionally, the absence/presence of KNaQ motifs in the host/parasite introduces an intriguing possibility of exploiting the KNaQ fold as a plausible antiparasitic drug target. The structure's unique shape and ion dependency and the possibility of controlling its folding by using low‐molecular‐weight ligands can be used for the design or discovery of novel recognition DNA elements and sensors.
A tetrastranded DNA structure, KNa‐quadruplex (KNaQ), is described. KNaQ forms from repetitive DNA sequences that are abundant in (parasitic) worms but extremely rare in humans or livestock. This opens a possibility of exploiting the fold as a plausible antiparasitic drug target. The structure's unique properties distinguish it from all other known DNA quadruplexes and can be used to design novel recognition DNA elements/sensors. |
doi_str_mv | 10.1002/ange.202313226 |
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A tetrastranded DNA structure, KNa‐quadruplex (KNaQ), is described. KNaQ forms from repetitive DNA sequences that are abundant in (parasitic) worms but extremely rare in humans or livestock. This opens a possibility of exploiting the fold as a plausible antiparasitic drug target. The structure's unique properties distinguish it from all other known DNA quadruplexes and can be used to design novel recognition DNA elements/sensors.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.202313226</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Antiparasitic agents ; Binding sites ; Deoxyribonucleic acid ; DNA ; DNA structure ; Drug screening ; Folding ; Gene expression ; Genomes ; Nanotechnology ; NMR spectroscopy ; Nucleotide sequence ; Parasites ; quadruplex ; telomere ; Telomeres ; Therapeutic targets ; unique cation dependency</subject><ispartof>Angewandte Chemie, 2024-02, Vol.136 (7), p.n/a</ispartof><rights>2023 The Authors. Angewandte Chemie published by Wiley-VCH GmbH</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1576-a2d1882db9c8cdfcfc69d22f0a623566ebc1038c2498ec555763fec297bc553c3</cites><orcidid>0000-0003-2837-4226 ; 0000-0001-5948-4837 ; 0000-0001-6501-4145 ; 0000-0001-6558-6186 ; 0000-0002-5470-8376 ; 0000-0003-2036-6512 ; 0000-0003-3043-8401</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fange.202313226$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fange.202313226$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids></links><search><creatorcontrib>Gajarsky, Martin</creatorcontrib><creatorcontrib>Stadlbauer, Petr</creatorcontrib><creatorcontrib>Sponer, Jiri</creatorcontrib><creatorcontrib>Cucchiarini, Anne</creatorcontrib><creatorcontrib>Dobrovolna, Michaela</creatorcontrib><creatorcontrib>Brazda, Vaclav</creatorcontrib><creatorcontrib>Mergny, Jean‐Louis</creatorcontrib><creatorcontrib>Trantirek, Lukas</creatorcontrib><creatorcontrib>Lenarcic Zivkovic, Martina</creatorcontrib><title>DNA Quadruplex Structure with a Unique Cation Dependency</title><title>Angewandte Chemie</title><description>DNA quadruplex structures provide an additional layer of regulatory control in genome maintenance and gene expression and are widely used in nanotechnology. We report the discovery of an unprecedented tetrastranded structure formed from a native G‐rich DNA sequence originating from the telomeric region of Caenorhabditis elegans. The structure is defined by multiple properties that distinguish it from all other known DNA quadruplexes. Most notably, the formation of a stable so‐called KNa‐quadruplex (KNaQ) requires concurrent coordination of K+ and Na+ ions at two distinct binding sites. This structure provides novel insight into G‐rich DNA folding under ionic conditions relevant to eukaryotic cell physiology and the structural evolution of telomeric DNA. It highlights the differences between the structural organization of human and nematode telomeric DNA, which should be considered when using C. elegans as a model in telomere biology, particularly in drug screening applications. Additionally, the absence/presence of KNaQ motifs in the host/parasite introduces an intriguing possibility of exploiting the KNaQ fold as a plausible antiparasitic drug target. The structure's unique shape and ion dependency and the possibility of controlling its folding by using low‐molecular‐weight ligands can be used for the design or discovery of novel recognition DNA elements and sensors.
A tetrastranded DNA structure, KNa‐quadruplex (KNaQ), is described. KNaQ forms from repetitive DNA sequences that are abundant in (parasitic) worms but extremely rare in humans or livestock. This opens a possibility of exploiting the fold as a plausible antiparasitic drug target. The structure's unique properties distinguish it from all other known DNA quadruplexes and can be used to design novel recognition DNA elements/sensors.</description><subject>Antiparasitic agents</subject><subject>Binding sites</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA structure</subject><subject>Drug screening</subject><subject>Folding</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Nanotechnology</subject><subject>NMR spectroscopy</subject><subject>Nucleotide sequence</subject><subject>Parasites</subject><subject>quadruplex</subject><subject>telomere</subject><subject>Telomeres</subject><subject>Therapeutic targets</subject><subject>unique cation dependency</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkMFLwzAUh4MoOKdXzwHPnclLmybHsc0pjInoziF7TbWjtjVt2fbfm1HRo6fHg9_33o-PkFvOJpwxuLfVu5sAA8EFgDwjI54Aj0SapOdkxFgcRwpifUmu2nbHGJOQ6hFR8_WUvvQ2831TugN97XyPXe8d3RfdB7V0UxVfvaMz2xV1ReeucVXmKjxek4vclq27-ZljsnlYvM0eo9Xz8mk2XUXIk1RGFjKuFGRbjQqzHHOUOgPImZUgEindFjkTCkMz5TBJAiNyh6DTbdgEijG5G-42vg5F2s7s6t5X4aUBDQBKcB6H1GRIoa_b1rvcNL74tP5oODMnO-Zkx_zaCYAegH1RuuM_aTNdLxd_7Dfe12ey</recordid><startdate>20240212</startdate><enddate>20240212</enddate><creator>Gajarsky, Martin</creator><creator>Stadlbauer, Petr</creator><creator>Sponer, Jiri</creator><creator>Cucchiarini, Anne</creator><creator>Dobrovolna, Michaela</creator><creator>Brazda, Vaclav</creator><creator>Mergny, Jean‐Louis</creator><creator>Trantirek, Lukas</creator><creator>Lenarcic Zivkovic, Martina</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-2837-4226</orcidid><orcidid>https://orcid.org/0000-0001-5948-4837</orcidid><orcidid>https://orcid.org/0000-0001-6501-4145</orcidid><orcidid>https://orcid.org/0000-0001-6558-6186</orcidid><orcidid>https://orcid.org/0000-0002-5470-8376</orcidid><orcidid>https://orcid.org/0000-0003-2036-6512</orcidid><orcidid>https://orcid.org/0000-0003-3043-8401</orcidid></search><sort><creationdate>20240212</creationdate><title>DNA Quadruplex Structure with a Unique Cation Dependency</title><author>Gajarsky, Martin ; Stadlbauer, Petr ; Sponer, Jiri ; Cucchiarini, Anne ; Dobrovolna, Michaela ; Brazda, Vaclav ; Mergny, Jean‐Louis ; Trantirek, Lukas ; Lenarcic Zivkovic, Martina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1576-a2d1882db9c8cdfcfc69d22f0a623566ebc1038c2498ec555763fec297bc553c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antiparasitic agents</topic><topic>Binding sites</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA structure</topic><topic>Drug screening</topic><topic>Folding</topic><topic>Gene expression</topic><topic>Genomes</topic><topic>Nanotechnology</topic><topic>NMR spectroscopy</topic><topic>Nucleotide sequence</topic><topic>Parasites</topic><topic>quadruplex</topic><topic>telomere</topic><topic>Telomeres</topic><topic>Therapeutic targets</topic><topic>unique cation dependency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gajarsky, Martin</creatorcontrib><creatorcontrib>Stadlbauer, Petr</creatorcontrib><creatorcontrib>Sponer, Jiri</creatorcontrib><creatorcontrib>Cucchiarini, Anne</creatorcontrib><creatorcontrib>Dobrovolna, Michaela</creatorcontrib><creatorcontrib>Brazda, Vaclav</creatorcontrib><creatorcontrib>Mergny, Jean‐Louis</creatorcontrib><creatorcontrib>Trantirek, Lukas</creatorcontrib><creatorcontrib>Lenarcic Zivkovic, Martina</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gajarsky, Martin</au><au>Stadlbauer, Petr</au><au>Sponer, Jiri</au><au>Cucchiarini, Anne</au><au>Dobrovolna, Michaela</au><au>Brazda, Vaclav</au><au>Mergny, Jean‐Louis</au><au>Trantirek, Lukas</au><au>Lenarcic Zivkovic, Martina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA Quadruplex Structure with a Unique Cation Dependency</atitle><jtitle>Angewandte Chemie</jtitle><date>2024-02-12</date><risdate>2024</risdate><volume>136</volume><issue>7</issue><epage>n/a</epage><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>DNA quadruplex structures provide an additional layer of regulatory control in genome maintenance and gene expression and are widely used in nanotechnology. We report the discovery of an unprecedented tetrastranded structure formed from a native G‐rich DNA sequence originating from the telomeric region of Caenorhabditis elegans. The structure is defined by multiple properties that distinguish it from all other known DNA quadruplexes. Most notably, the formation of a stable so‐called KNa‐quadruplex (KNaQ) requires concurrent coordination of K+ and Na+ ions at two distinct binding sites. This structure provides novel insight into G‐rich DNA folding under ionic conditions relevant to eukaryotic cell physiology and the structural evolution of telomeric DNA. It highlights the differences between the structural organization of human and nematode telomeric DNA, which should be considered when using C. elegans as a model in telomere biology, particularly in drug screening applications. Additionally, the absence/presence of KNaQ motifs in the host/parasite introduces an intriguing possibility of exploiting the KNaQ fold as a plausible antiparasitic drug target. The structure's unique shape and ion dependency and the possibility of controlling its folding by using low‐molecular‐weight ligands can be used for the design or discovery of novel recognition DNA elements and sensors.
A tetrastranded DNA structure, KNa‐quadruplex (KNaQ), is described. KNaQ forms from repetitive DNA sequences that are abundant in (parasitic) worms but extremely rare in humans or livestock. This opens a possibility of exploiting the fold as a plausible antiparasitic drug target. The structure's unique properties distinguish it from all other known DNA quadruplexes and can be used to design novel recognition DNA elements/sensors.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.202313226</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2837-4226</orcidid><orcidid>https://orcid.org/0000-0001-5948-4837</orcidid><orcidid>https://orcid.org/0000-0001-6501-4145</orcidid><orcidid>https://orcid.org/0000-0001-6558-6186</orcidid><orcidid>https://orcid.org/0000-0002-5470-8376</orcidid><orcidid>https://orcid.org/0000-0003-2036-6512</orcidid><orcidid>https://orcid.org/0000-0003-3043-8401</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antiparasitic agents Binding sites Deoxyribonucleic acid DNA DNA structure Drug screening Folding Gene expression Genomes Nanotechnology NMR spectroscopy Nucleotide sequence Parasites quadruplex telomere Telomeres Therapeutic targets unique cation dependency |
title | DNA Quadruplex Structure with a Unique Cation Dependency |
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