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Base Pair Stability of 8-Chloro- and 8-Iodo-2‘-deoxyguanosine Opposite 2‘-Deoxycytidine: Implications Regarding the Bioactivity of 8-Oxo-2‘-deoxyguanosine
8-Oxo-2‘-deoxyguanosine (OdG) is an abundant and promutagenic damaged nucleotide that has been linked to aging and disease. To gain insight into the alternate base pairings of OdG, 8-chloro- and 8-iodo-2‘-deoxyguanosine were incorporated into oligonucleotides and, along with 2‘-deoxyguanosine and 8-...
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Published in: | Journal of the American Chemical Society 2005-09, Vol.127 (35), p.12220-12221 |
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container_title | Journal of the American Chemical Society |
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creator | Hamm, Michelle L Rajguru, Sumika Downs, Anthony M Cholera, Rushina |
description | 8-Oxo-2‘-deoxyguanosine (OdG) is an abundant and promutagenic damaged nucleotide that has been linked to aging and disease. To gain insight into the alternate base pairings of OdG, 8-chloro- and 8-iodo-2‘-deoxyguanosine were incorporated into oligonucleotides and, along with 2‘-deoxyguanosine and 8-bromo-2‘-deoxyguanosine, were tested for their stability in base pairs opposite dC. We found a strong correlation between increased atomic radius and bond length at C8 and decreased base pair stability. These findings along with NMR studies on the base conformation of the corresponding nucleosides support the theory that the steric bulk of the 8-oxygen plays a role in OdG mutation and disease. |
doi_str_mv | 10.1021/ja052578k |
format | article |
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These findings along with NMR studies on the base conformation of the corresponding nucleosides support the theory that the steric bulk of the 8-oxygen plays a role in OdG mutation and disease.</description><subject>Base Pairing</subject><subject>Base Sequence</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cytosine - analogs & derivatives</subject><subject>Cytosine - chemistry</subject><subject>Cytosine - metabolism</subject><subject>Deoxyguanosine - analogs & derivatives</subject><subject>Deoxyguanosine - chemistry</subject><subject>Deoxyguanosine - metabolism</subject><subject>Hydrogen Bonding</subject><subject>Models, Chemical</subject><subject>Nucleic Acid Conformation</subject><subject>Transition Temperature</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNptkcFuEzEURS0EoqGw4AeQNyCxMIztscdm1wZSgiqlIoWt5Xg8qdPJeLA9KNl1yx-w58_6JTgkCpuu7Kdz9K70LgAvcfEOFwS_X-mCEVaJ20dghBkpEMOEPwajoigIqgSnJ-BZjKs8lkTgp-AEc0wxFnIE_pzraOGVdgHOk1641qUt9A0UaHzT-uAR1F2dp6mvPSL3d79Rbf1muxx056PrLJz1ff4kC__BjztotsnVmX24v_sFp-u-dUYn57sIv9qlDhktYbqx8Nx5bZL7eYycbR7MeA6eNLqN9sXhPQXfJp-ux5_R5exiOj67RLrEVUIGC8GNkYwVmktdVVY0ZVnXuDacyppaIzWjpawkxtiUstSEcS44qRYNlYTTU_Bmv7cP_sdgY1JrF41tW91ZP0TFBaP5cCyLb_eiCT7GYBvVB7fWYatwoXaNqGMj2X11WDos1rb-bx4qyALaCy4muzlyHW4Vr2jF1PXVXE3EhH6_-DJXu_DXe1-bqFZ-CF2-yQPBfwFpW6VR</recordid><startdate>20050907</startdate><enddate>20050907</enddate><creator>Hamm, Michelle L</creator><creator>Rajguru, Sumika</creator><creator>Downs, Anthony M</creator><creator>Cholera, Rushina</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050907</creationdate><title>Base Pair Stability of 8-Chloro- and 8-Iodo-2‘-deoxyguanosine Opposite 2‘-Deoxycytidine: Implications Regarding the Bioactivity of 8-Oxo-2‘-deoxyguanosine</title><author>Hamm, Michelle L ; Rajguru, Sumika ; Downs, Anthony M ; Cholera, Rushina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a417t-c1886cc9550a69a77e8f44dd1dc639d3ec9a534979111c494a25668627bf39263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Base Pairing</topic><topic>Base Sequence</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Cytosine - analogs & derivatives</topic><topic>Cytosine - chemistry</topic><topic>Cytosine - metabolism</topic><topic>Deoxyguanosine - analogs & derivatives</topic><topic>Deoxyguanosine - chemistry</topic><topic>Deoxyguanosine - metabolism</topic><topic>Hydrogen Bonding</topic><topic>Models, Chemical</topic><topic>Nucleic Acid Conformation</topic><topic>Transition Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hamm, Michelle L</creatorcontrib><creatorcontrib>Rajguru, Sumika</creatorcontrib><creatorcontrib>Downs, Anthony M</creatorcontrib><creatorcontrib>Cholera, Rushina</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hamm, Michelle L</au><au>Rajguru, Sumika</au><au>Downs, Anthony M</au><au>Cholera, Rushina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Base Pair Stability of 8-Chloro- and 8-Iodo-2‘-deoxyguanosine Opposite 2‘-Deoxycytidine: Implications Regarding the Bioactivity of 8-Oxo-2‘-deoxyguanosine</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2005-09-07</date><risdate>2005</risdate><volume>127</volume><issue>35</issue><spage>12220</spage><epage>12221</epage><pages>12220-12221</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>8-Oxo-2‘-deoxyguanosine (OdG) is an abundant and promutagenic damaged nucleotide that has been linked to aging and disease. To gain insight into the alternate base pairings of OdG, 8-chloro- and 8-iodo-2‘-deoxyguanosine were incorporated into oligonucleotides and, along with 2‘-deoxyguanosine and 8-bromo-2‘-deoxyguanosine, were tested for their stability in base pairs opposite dC. We found a strong correlation between increased atomic radius and bond length at C8 and decreased base pair stability. These findings along with NMR studies on the base conformation of the corresponding nucleosides support the theory that the steric bulk of the 8-oxygen plays a role in OdG mutation and disease.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>16131189</pmid><doi>10.1021/ja052578k</doi><tpages>2</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Base Pairing Base Sequence Chromatography, High Pressure Liquid Cytosine - analogs & derivatives Cytosine - chemistry Cytosine - metabolism Deoxyguanosine - analogs & derivatives Deoxyguanosine - chemistry Deoxyguanosine - metabolism Hydrogen Bonding Models, Chemical Nucleic Acid Conformation Transition Temperature |
title | Base Pair Stability of 8-Chloro- and 8-Iodo-2‘-deoxyguanosine Opposite 2‘-Deoxycytidine: Implications Regarding the Bioactivity of 8-Oxo-2‘-deoxyguanosine |
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