Specific triplex binding capacity of mixed base sequence duplex nucleic acids used for single-nucleotide polymorphism detection
Specific base recognition and binding between native double-stranded DNA (dsDNA) and complementary single-stranded DNA (ssDNA) of mixed base sequence is presented. Third-strand binding, facilitated and stabilized by a DNA intercalator, YOYO-1, occurs within 5 min at room temperature. This triplex bi...
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Veröffentlicht in: | Genetic testing 2005-06, Vol.9 (2), p.111-120 |
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description | Specific base recognition and binding between native double-stranded DNA (dsDNA) and complementary single-stranded DNA (ssDNA) of mixed base sequence is presented. Third-strand binding, facilitated and stabilized by a DNA intercalator, YOYO-1, occurs within 5 min at room temperature. This triplex binding capability has been used to develop a homogeneous assay that accurately detects 1-, 2-, or 3-bp mutations or deletions in the dsDNA target. Every type of 1-bp mismatch can be identified. The assay can reliably distinguish homozygous from heterozygous polymerase chain reaction (PCR)-amplified genomic dsDNA, thus providing a highly sensitive clinical diagnostic assay. |
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The assay can reliably distinguish homozygous from heterozygous polymerase chain reaction (PCR)-amplified genomic dsDNA, thus providing a highly sensitive clinical diagnostic assay.</description><subject>Base Pairing</subject><subject>Benzoxazoles</subject><subject>Chromatography, High Pressure Liquid</subject><subject>DNA</subject><subject>DNA, Single-Stranded</subject><subject>Fluorescent Dyes</subject><subject>Intercalating Agents</subject><subject>Mutation</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Quinolinium Compounds</subject><subject>Spectrometry, Fluorescence</subject><subject>Time Factors</subject><issn>1090-6576</issn><issn>1557-7473</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkElLxEAQRhtRHLerR-mTt8SuZJJOHUXcYMCDem56qWhLko7pBJyTf93MAp6qoN73QT3GLkGkICq8-RgpzYQoUkwB4ICdQFHIRC5lfjjvAkVSFrJcsNMYv4QQFYjsmC2gwGVeFOKE_b72ZH3tLR8H3zf0w43vnO8-uNW9tn5c81Dz1v-Q40ZH4pG-J-oscTdt8W6yDc3xmXWRT3Hm6jDwOFc0lGyvYfSOeB-adRuG_tPHljsayY4-dOfsqNZNpIv9PGPvD_dvd0_J6uXx-e52ldgM8zFBo02ZOUnOEtZlnpEAU-VYI0nUKIXBWhuDWpZmaauqkqDRLCsE4UwJLj9j17vefgjzA3FUrY-WmkZ3FKaoSokZ5AAzmO5AO4QYB6pVP_hWD2sFQm2Uq1m52ihXqGAbuNo3T6Yl94_vHed_n-OAmA</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Daksis, Jasmine I</creator><creator>Erikson, Glen H</creator><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>20050601</creationdate><title>Specific triplex binding capacity of mixed base sequence duplex nucleic acids used for single-nucleotide polymorphism detection</title><author>Daksis, Jasmine I ; Erikson, Glen H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c293t-9bab62d7edce9f632e01b839f9e79a970b9fabb9a76b4c88871a9b48910db61d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Base Pairing</topic><topic>Benzoxazoles</topic><topic>Chromatography, High Pressure Liquid</topic><topic>DNA</topic><topic>DNA, Single-Stranded</topic><topic>Fluorescent Dyes</topic><topic>Intercalating Agents</topic><topic>Mutation</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Quinolinium Compounds</topic><topic>Spectrometry, Fluorescence</topic><topic>Time Factors</topic><toplevel>online_resources</toplevel><creatorcontrib>Daksis, Jasmine I</creatorcontrib><creatorcontrib>Erikson, Glen H</creatorcontrib><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>Genetic testing</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daksis, Jasmine I</au><au>Erikson, Glen H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specific triplex binding capacity of mixed base sequence duplex nucleic acids used for single-nucleotide polymorphism detection</atitle><jtitle>Genetic testing</jtitle><addtitle>Genet Test</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>9</volume><issue>2</issue><spage>111</spage><epage>120</epage><pages>111-120</pages><issn>1090-6576</issn><eissn>1557-7473</eissn><abstract>Specific base recognition and binding between native double-stranded DNA (dsDNA) and complementary single-stranded DNA (ssDNA) of mixed base sequence is presented. 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subjects | Base Pairing Benzoxazoles Chromatography, High Pressure Liquid DNA DNA, Single-Stranded Fluorescent Dyes Intercalating Agents Mutation Polymorphism, Single Nucleotide Quinolinium Compounds Spectrometry, Fluorescence Time Factors |
title | Specific triplex binding capacity of mixed base sequence duplex nucleic acids used for single-nucleotide polymorphism detection |
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