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Endogenous oxidative DNA base modifications analysed with repair enzymes and GC/MS technique
GC/MS technique was used to identify endogenous levels of oxidatively modified DNA bases. To avoid possible artefact formation we used Fpg and Endo III endonucleases instead of acid hydrolysis to liberate the base products from unmodified DNA samples. Several different DNA preparations were used: (i...
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Published in: | Nucleic acids research 2000-03, Vol.28 (6), p.E16-16 |
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creator | Jaruga, P Speina, E Gackowski, D Tudek, B Olinski, R |
description | GC/MS technique was used to identify endogenous levels of oxidatively modified DNA bases. To avoid possible artefact formation we used Fpg and Endo III endonucleases instead of acid hydrolysis to liberate the base products from unmodified DNA samples. Several different DNA preparations were used: (i) commercial calf thymus DNA, (ii) DNA isolated from rat liver, (iii) DNA isolated from human lymphocytes and (iv) nuclei isolated from rat liver. In all DNA samples used in our assays the most efficiently removed bases by Fpg protein are FapyG and FapyA although 8-oxoG was also detected in all preparations. The amount of 8-oxoG in human lymphocytes and in rat liver DNA was 3 and 2 per 10(7)bases, respectively. It is reasonable to postulate that the presented method is one of the techniques which should be used to reveal the enigma of endogenous, oxidative DNA damage. |
doi_str_mv | 10.1093/nar/28.6.e16 |
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To avoid possible artefact formation we used Fpg and Endo III endonucleases instead of acid hydrolysis to liberate the base products from unmodified DNA samples. Several different DNA preparations were used: (i) commercial calf thymus DNA, (ii) DNA isolated from rat liver, (iii) DNA isolated from human lymphocytes and (iv) nuclei isolated from rat liver. In all DNA samples used in our assays the most efficiently removed bases by Fpg protein are FapyG and FapyA although 8-oxoG was also detected in all preparations. The amount of 8-oxoG in human lymphocytes and in rat liver DNA was 3 and 2 per 10(7)bases, respectively. It is reasonable to postulate that the presented method is one of the techniques which should be used to reveal the enigma of endogenous, oxidative DNA damage.</description><identifier>ISSN: 1362-4962</identifier><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/28.6.e16</identifier><identifier>PMID: 10684948</identifier><identifier>CODEN: NARHAD</identifier><language>eng</language><publisher>England: Oxford Publishing Limited (England)</publisher><subject>8-oxo-guanine ; Animals ; Cattle ; Deoxyribonuclease (Pyrimidine Dimer) ; DNA - metabolism ; DNA Damage ; DNA Repair ; DNA-Formamidopyrimidine Glycosylase ; Endo III endonuclease ; Endodeoxyribonucleases - metabolism ; Escherichia coli Proteins ; FapyA protein ; FapyG protein ; Fpg endonuclease ; Free Radicals ; Gas Chromatography-Mass Spectrometry ; Humans ; N-Glycosyl Hydrolases - metabolism ; NAR Methods Online ; Oxidation-Reduction ; Rats</subject><ispartof>Nucleic acids research, 2000-03, Vol.28 (6), p.E16-16</ispartof><rights>Copyright Oxford University Press(England) Mar 15, 2000</rights><rights>Copyright © 2000 Oxford University Press 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-2127195c35ba7ce29605d877e31268a333fd3fe3d159fb598e203391b579a7203</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC111057/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC111057/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10684948$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jaruga, P</creatorcontrib><creatorcontrib>Speina, E</creatorcontrib><creatorcontrib>Gackowski, D</creatorcontrib><creatorcontrib>Tudek, B</creatorcontrib><creatorcontrib>Olinski, R</creatorcontrib><title>Endogenous oxidative DNA base modifications analysed with repair enzymes and GC/MS technique</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>GC/MS technique was used to identify endogenous levels of oxidatively modified DNA bases. To avoid possible artefact formation we used Fpg and Endo III endonucleases instead of acid hydrolysis to liberate the base products from unmodified DNA samples. Several different DNA preparations were used: (i) commercial calf thymus DNA, (ii) DNA isolated from rat liver, (iii) DNA isolated from human lymphocytes and (iv) nuclei isolated from rat liver. In all DNA samples used in our assays the most efficiently removed bases by Fpg protein are FapyG and FapyA although 8-oxoG was also detected in all preparations. The amount of 8-oxoG in human lymphocytes and in rat liver DNA was 3 and 2 per 10(7)bases, respectively. It is reasonable to postulate that the presented method is one of the techniques which should be used to reveal the enigma of endogenous, oxidative DNA damage.</description><subject>8-oxo-guanine</subject><subject>Animals</subject><subject>Cattle</subject><subject>Deoxyribonuclease (Pyrimidine Dimer)</subject><subject>DNA - metabolism</subject><subject>DNA Damage</subject><subject>DNA Repair</subject><subject>DNA-Formamidopyrimidine Glycosylase</subject><subject>Endo III endonuclease</subject><subject>Endodeoxyribonucleases - metabolism</subject><subject>Escherichia coli Proteins</subject><subject>FapyA protein</subject><subject>FapyG protein</subject><subject>Fpg endonuclease</subject><subject>Free Radicals</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Humans</subject><subject>N-Glycosyl Hydrolases - metabolism</subject><subject>NAR Methods Online</subject><subject>Oxidation-Reduction</subject><subject>Rats</subject><issn>1362-4962</issn><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkU1vEzEQhq2Kql9w67myOHBqEn-s7fWBQxVKW6nAAbghWd71bONq107tTSH8-jpKVaVcOM1o5pnRO_MidErJlBLNZ8GmGauncgpU7qEjyiWbVFqyNzv5ITrO-Z4QWlFRHaBDSmRd6ao-Qr8ug4t3EOIq4_jHOzv6R8Cfvl7gxmbAQ3S-822pxpCxDbZfZ3D4tx8XOMHS-oQh_F0PsGk6fDWfffmOR2gXwT-s4C3a72yf4d1zPEE_P1_-mF9Pbr9d3cwvbidtJeU4YZQpqkXLRWNVC0xLIlytFHDKZG05553jHXBHhe4aoWtghHNNG6G0VSU_QR-3e5erZgDXQhiT7c0y-cGmtYnWm9ed4BfmLj4aSikRqsx_eJ5PscjOoxl8bqHvbYDyGKOIZpJL-V-QKsGLPl3A9_-A93GVyvuyYYQIoVm12Xa-hdoUc07QvSimxGy8NcVbw2ojTfG24Ge7V-7AWzP5E5mnoAU</recordid><startdate>20000315</startdate><enddate>20000315</enddate><creator>Jaruga, P</creator><creator>Speina, E</creator><creator>Gackowski, D</creator><creator>Tudek, B</creator><creator>Olinski, R</creator><general>Oxford Publishing Limited (England)</general><general>Oxford University Press</general><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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20000315</creationdate><title>Endogenous oxidative DNA base modifications analysed with repair enzymes and GC/MS technique</title><author>Jaruga, P ; 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To avoid possible artefact formation we used Fpg and Endo III endonucleases instead of acid hydrolysis to liberate the base products from unmodified DNA samples. Several different DNA preparations were used: (i) commercial calf thymus DNA, (ii) DNA isolated from rat liver, (iii) DNA isolated from human lymphocytes and (iv) nuclei isolated from rat liver. In all DNA samples used in our assays the most efficiently removed bases by Fpg protein are FapyG and FapyA although 8-oxoG was also detected in all preparations. The amount of 8-oxoG in human lymphocytes and in rat liver DNA was 3 and 2 per 10(7)bases, respectively. It is reasonable to postulate that the presented method is one of the techniques which should be used to reveal the enigma of endogenous, oxidative DNA damage.</abstract><cop>England</cop><pub>Oxford Publishing Limited (England)</pub><pmid>10684948</pmid><doi>10.1093/nar/28.6.e16</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 8-oxo-guanine Animals Cattle Deoxyribonuclease (Pyrimidine Dimer) DNA - metabolism DNA Damage DNA Repair DNA-Formamidopyrimidine Glycosylase Endo III endonuclease Endodeoxyribonucleases - metabolism Escherichia coli Proteins FapyA protein FapyG protein Fpg endonuclease Free Radicals Gas Chromatography-Mass Spectrometry Humans N-Glycosyl Hydrolases - metabolism NAR Methods Online Oxidation-Reduction Rats |
title | Endogenous oxidative DNA base modifications analysed with repair enzymes and GC/MS technique |
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