Loading…

Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes

High-resolution two-dimensional NMR studies have been completed on the self-complementary d(C-G-C-G-A-G-C-T-T-G-C-G) duplex (designated G.T 12-mer) and the self-complementary d(C-G-C-G-A-G-C-T-O4meT-G-C-G) duplex (designated G.O4meT 12-mer) containing G.T and G.O4meT pairs at identical positions fou...

Full description

Saved in:
Bibliographic Details
Published in:Biochemistry (Easton) 1988-01, Vol.27 (1), p.108
Main Authors: Kalnik, M W, Kouchakdjian, M, Li, B F, Swann, P F, Patel, D J
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue 1
container_start_page 108
container_title Biochemistry (Easton)
container_volume 27
creator Kalnik, M W
Kouchakdjian, M
Li, B F
Swann, P F
Patel, D J
description High-resolution two-dimensional NMR studies have been completed on the self-complementary d(C-G-C-G-A-G-C-T-T-G-C-G) duplex (designated G.T 12-mer) and the self-complementary d(C-G-C-G-A-G-C-T-O4meT-G-C-G) duplex (designated G.O4meT 12-mer) containing G.T and G.O4meT pairs at identical positions four base pairs in from either end of the duplex. The exchangeable and nonexchangeable proton resonances have been assigned from an analysis of two-dimensional nuclear Overhauser enhancement (NOESY) spectra for the G.T 12-mer and G.O4meT 12-mer duplexes in H2O and D2O solution. The guanosine and thymidine imino protons in the G.T mismatch resonate at 10.57 and 11.98 ppm, respectively, and exhibit a strong NOE between themselves and to imino protons of flanking base pairs in the G.T 12-mer duplex. These results are consistent with wobble pairing at the G.T mismatch site involving two imino proton-carbonyl hydrogen bonds as reported previously [Hare, D. R., Shapiro, L., & Patel, D. J. (1986) Biochemistry 25, 7445-7456]. In contrast, the guanosine imino proton in the G.O4meT pair resonates at 8.67 ppm. The large upfield chemical shift of this proton relative to that of the imino proton resonance of G in the G.T mismatch or in G.C base pairs indicates that hydrogen bonding to O4meT is either very weak or absent. This guanosine imino proton has an NOE to the OCH3 group of O4meT across the pair and NOEs to the imino protons of flanking base pairs.
doi_str_mv 10.1021/bi00401a018
format article
fullrecord <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_3349021</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3349021</sourcerecordid><originalsourceid>FETCH-LOGICAL-p138t-ac1d6630cd5003dd288e4b171cd2d04f5320214262d3ef65980de39311e41d473</originalsourceid><addsrcrecordid>eNotkEtPwkAUhWehQURXrk3mDxTvPPpyh4hogpCYuibTubc4hj7SaRNZ-dctyOoszndOcg5jdwKmAqR4yB2ABmFAJBdsDABRINMIrti1999w9GI9YiOldDrgY_b7ZDzxxriWl86XprNf5LmpkFvTWlfVO6qCskZXOEKeD7DnruLP69njQPH1-wf3XY8HXhd8Oc1OyeV0o0vKTq2u2h15rJGsqXq7p7pzSBz7Zk8_5G_YZWH2nm7POmGfL4ts_hqsNsu3-WwVNEIlXWCswChSYDEEUIgySUjnIhYWJYIuQiWHOVpGEhUVUZgmgKRSJQRpgTpWE3b_39v0eUm4bVpXmvawPR-h_gDvXVwx</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes</title><source>American Chemical Society</source><creator>Kalnik, M W ; Kouchakdjian, M ; Li, B F ; Swann, P F ; Patel, D J</creator><creatorcontrib>Kalnik, M W ; Kouchakdjian, M ; Li, B F ; Swann, P F ; Patel, D J</creatorcontrib><description>High-resolution two-dimensional NMR studies have been completed on the self-complementary d(C-G-C-G-A-G-C-T-T-G-C-G) duplex (designated G.T 12-mer) and the self-complementary d(C-G-C-G-A-G-C-T-O4meT-G-C-G) duplex (designated G.O4meT 12-mer) containing G.T and G.O4meT pairs at identical positions four base pairs in from either end of the duplex. The exchangeable and nonexchangeable proton resonances have been assigned from an analysis of two-dimensional nuclear Overhauser enhancement (NOESY) spectra for the G.T 12-mer and G.O4meT 12-mer duplexes in H2O and D2O solution. The guanosine and thymidine imino protons in the G.T mismatch resonate at 10.57 and 11.98 ppm, respectively, and exhibit a strong NOE between themselves and to imino protons of flanking base pairs in the G.T 12-mer duplex. These results are consistent with wobble pairing at the G.T mismatch site involving two imino proton-carbonyl hydrogen bonds as reported previously [Hare, D. R., Shapiro, L., &amp; Patel, D. J. (1986) Biochemistry 25, 7445-7456]. In contrast, the guanosine imino proton in the G.O4meT pair resonates at 8.67 ppm. The large upfield chemical shift of this proton relative to that of the imino proton resonance of G in the G.T mismatch or in G.C base pairs indicates that hydrogen bonding to O4meT is either very weak or absent. This guanosine imino proton has an NOE to the OCH3 group of O4meT across the pair and NOEs to the imino protons of flanking base pairs.</description><identifier>ISSN: 0006-2960</identifier><identifier>DOI: 10.1021/bi00401a018</identifier><identifier>PMID: 3349021</identifier><language>eng</language><publisher>United States</publisher><subject>Base Composition ; Base Sequence ; Carcinogens ; DNA ; Guanine ; Hydrogen Bonding ; Magnetic Resonance Spectroscopy ; Models, Molecular ; Nucleic Acid Conformation ; Oligodeoxyribonucleotides ; Thymidine - analogs &amp; derivatives ; Thymine</subject><ispartof>Biochemistry (Easton), 1988-01, Vol.27 (1), p.108</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3349021$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kalnik, M W</creatorcontrib><creatorcontrib>Kouchakdjian, M</creatorcontrib><creatorcontrib>Li, B F</creatorcontrib><creatorcontrib>Swann, P F</creatorcontrib><creatorcontrib>Patel, D J</creatorcontrib><title>Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes</title><title>Biochemistry (Easton)</title><addtitle>Biochemistry</addtitle><description>High-resolution two-dimensional NMR studies have been completed on the self-complementary d(C-G-C-G-A-G-C-T-T-G-C-G) duplex (designated G.T 12-mer) and the self-complementary d(C-G-C-G-A-G-C-T-O4meT-G-C-G) duplex (designated G.O4meT 12-mer) containing G.T and G.O4meT pairs at identical positions four base pairs in from either end of the duplex. The exchangeable and nonexchangeable proton resonances have been assigned from an analysis of two-dimensional nuclear Overhauser enhancement (NOESY) spectra for the G.T 12-mer and G.O4meT 12-mer duplexes in H2O and D2O solution. The guanosine and thymidine imino protons in the G.T mismatch resonate at 10.57 and 11.98 ppm, respectively, and exhibit a strong NOE between themselves and to imino protons of flanking base pairs in the G.T 12-mer duplex. These results are consistent with wobble pairing at the G.T mismatch site involving two imino proton-carbonyl hydrogen bonds as reported previously [Hare, D. R., Shapiro, L., &amp; Patel, D. J. (1986) Biochemistry 25, 7445-7456]. In contrast, the guanosine imino proton in the G.O4meT pair resonates at 8.67 ppm. The large upfield chemical shift of this proton relative to that of the imino proton resonance of G in the G.T mismatch or in G.C base pairs indicates that hydrogen bonding to O4meT is either very weak or absent. This guanosine imino proton has an NOE to the OCH3 group of O4meT across the pair and NOEs to the imino protons of flanking base pairs.</description><subject>Base Composition</subject><subject>Base Sequence</subject><subject>Carcinogens</subject><subject>DNA</subject><subject>Guanine</subject><subject>Hydrogen Bonding</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Models, Molecular</subject><subject>Nucleic Acid Conformation</subject><subject>Oligodeoxyribonucleotides</subject><subject>Thymidine - analogs &amp; derivatives</subject><subject>Thymine</subject><issn>0006-2960</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNotkEtPwkAUhWehQURXrk3mDxTvPPpyh4hogpCYuibTubc4hj7SaRNZ-dctyOoszndOcg5jdwKmAqR4yB2ABmFAJBdsDABRINMIrti1999w9GI9YiOldDrgY_b7ZDzxxriWl86XprNf5LmpkFvTWlfVO6qCskZXOEKeD7DnruLP69njQPH1-wf3XY8HXhd8Oc1OyeV0o0vKTq2u2h15rJGsqXq7p7pzSBz7Zk8_5G_YZWH2nm7POmGfL4ts_hqsNsu3-WwVNEIlXWCswChSYDEEUIgySUjnIhYWJYIuQiWHOVpGEhUVUZgmgKRSJQRpgTpWE3b_39v0eUm4bVpXmvawPR-h_gDvXVwx</recordid><startdate>19880112</startdate><enddate>19880112</enddate><creator>Kalnik, M W</creator><creator>Kouchakdjian, M</creator><creator>Li, B F</creator><creator>Swann, P F</creator><creator>Patel, D J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19880112</creationdate><title>Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes</title><author>Kalnik, M W ; Kouchakdjian, M ; Li, B F ; Swann, P F ; Patel, D J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p138t-ac1d6630cd5003dd288e4b171cd2d04f5320214262d3ef65980de39311e41d473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Base Composition</topic><topic>Base Sequence</topic><topic>Carcinogens</topic><topic>DNA</topic><topic>Guanine</topic><topic>Hydrogen Bonding</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Models, Molecular</topic><topic>Nucleic Acid Conformation</topic><topic>Oligodeoxyribonucleotides</topic><topic>Thymidine - analogs &amp; derivatives</topic><topic>Thymine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalnik, M W</creatorcontrib><creatorcontrib>Kouchakdjian, M</creatorcontrib><creatorcontrib>Li, B F</creatorcontrib><creatorcontrib>Swann, P F</creatorcontrib><creatorcontrib>Patel, D J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Biochemistry (Easton)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalnik, M W</au><au>Kouchakdjian, M</au><au>Li, B F</au><au>Swann, P F</au><au>Patel, D J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>1988-01-12</date><risdate>1988</risdate><volume>27</volume><issue>1</issue><spage>108</spage><pages>108-</pages><issn>0006-2960</issn><abstract>High-resolution two-dimensional NMR studies have been completed on the self-complementary d(C-G-C-G-A-G-C-T-T-G-C-G) duplex (designated G.T 12-mer) and the self-complementary d(C-G-C-G-A-G-C-T-O4meT-G-C-G) duplex (designated G.O4meT 12-mer) containing G.T and G.O4meT pairs at identical positions four base pairs in from either end of the duplex. The exchangeable and nonexchangeable proton resonances have been assigned from an analysis of two-dimensional nuclear Overhauser enhancement (NOESY) spectra for the G.T 12-mer and G.O4meT 12-mer duplexes in H2O and D2O solution. The guanosine and thymidine imino protons in the G.T mismatch resonate at 10.57 and 11.98 ppm, respectively, and exhibit a strong NOE between themselves and to imino protons of flanking base pairs in the G.T 12-mer duplex. These results are consistent with wobble pairing at the G.T mismatch site involving two imino proton-carbonyl hydrogen bonds as reported previously [Hare, D. R., Shapiro, L., &amp; Patel, D. J. (1986) Biochemistry 25, 7445-7456]. In contrast, the guanosine imino proton in the G.O4meT pair resonates at 8.67 ppm. The large upfield chemical shift of this proton relative to that of the imino proton resonance of G in the G.T mismatch or in G.C base pairs indicates that hydrogen bonding to O4meT is either very weak or absent. This guanosine imino proton has an NOE to the OCH3 group of O4meT across the pair and NOEs to the imino protons of flanking base pairs.</abstract><cop>United States</cop><pmid>3349021</pmid><doi>10.1021/bi00401a018</doi></addata></record>
fulltext fulltext
identifier ISSN: 0006-2960
ispartof Biochemistry (Easton), 1988-01, Vol.27 (1), p.108
issn 0006-2960
language eng
recordid cdi_pubmed_primary_3349021
source American Chemical Society
subjects Base Composition
Base Sequence
Carcinogens
DNA
Guanine
Hydrogen Bonding
Magnetic Resonance Spectroscopy
Models, Molecular
Nucleic Acid Conformation
Oligodeoxyribonucleotides
Thymidine - analogs & derivatives
Thymine
title Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T21%3A03%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Base%20pair%20mismatches%20and%20carcinogen-modified%20bases%20in%20DNA:%20an%20NMR%20study%20of%20G.T%20and%20G.O4meT%20pairing%20in%20dodecanucleotide%20duplexes&rft.jtitle=Biochemistry%20(Easton)&rft.au=Kalnik,%20M%20W&rft.date=1988-01-12&rft.volume=27&rft.issue=1&rft.spage=108&rft.pages=108-&rft.issn=0006-2960&rft_id=info:doi/10.1021/bi00401a018&rft_dat=%3Cpubmed%3E3349021%3C/pubmed%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p138t-ac1d6630cd5003dd288e4b171cd2d04f5320214262d3ef65980de39311e41d473%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/3349021&rfr_iscdi=true