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dc.contributor.authorWolfe, Jia Liu
dc.contributor.authorKawate, Tomohiko
dc.contributor.authorSarracino, David A.
dc.contributor.authorZillmann, Martin
dc.contributor.authorOlson, Jeffrey
dc.contributor.authorStanton, Vincent P. Jr.
dc.contributor.authorVerdine, Gregory L.
dc.date.accessioned2019-10-09T13:57:07Z
dc.date.issued2002
dc.identifier.citationWolfe, J. L., T. Kawate, D. A. Sarracino, M. Zillmann, J. Olson, V. P. Stanton, and G. L. Verdine. 2002. “A Genotyping Strategy Based on Incorporation and Cleavage of Chemically Modified Nucleotides.” Proceedings of the National Academy of Sciences99 (17): 11073–78. https://doi.org/10.1073/pnas.162346699.
dc.identifier.issn0027-8424
dc.identifier.issn0744-2831
dc.identifier.issn1091-6490
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:41511306*
dc.description.abstractAiming to facilitate the analysis of human genetic variations in the context of disease susceptibility and varied drug response, we have developed a genotyping method that entails incorporation of a chemically labile nucleotide by PCR followed by specific chemical cleavage of the resulting amplicon at the modified bases. The identity of the cleaved fragments determines the genotype of the DNA. This method, termed Incorporation and Complete Chemical Cleavage, utilizes modified nucleotides 7-deaza-7-nitro-dATP, 7-deaza-7-nitro-dGTP, 5-hydroxy-dCTP, and 5-hydroxy-dUTP, which have increased chemical reactivity but are able to form standard Watson-Crick base pairs. Thus one analog is substituted for the corresponding nucleotide during PCR, generating amplicons that contain nucleotide analogs at each occurrence of the selected base throughout the target DNA except for the primer sequences. Subsequent treatment with an oxidant followed by an organic base results in chemical cleavage at each site of modification, which produces fragments of different lengths and/or molecular weights that reflect the genotype of the original DNA sample at the site of interest. This incorporation and cleavage chemistry are widely applicable to many existing nucleic acid analysis platforms, including gel electrophoresis and mass spectrometry. By combining DNA amplification and analog incorporation into one step, this strategy eliminates preamplification, DNA-strand separation, primer extension, and purification procedures associated with traditional chain-termination chemistry and therefore presents significant advantages in terms of speed, cost, and simplicity of genotyping.
dc.language.isoen_US
dc.publisherNational Academy of Sciences
dash.licenseLAA
dc.titleA genotyping strategy based on incorporation and cleavage of chemically modified nucleotides
dc.typeJournal Article
dc.description.versionVersion of Record
dc.relation.journalProceedings of the National Academy of Sciences of the United States of America
dash.depositing.authorVerdine, Gregory L.::b80a6eb8a9fb2d98773ce5b5cc1dd993::600
dc.date.available2019-10-09T13:57:07Z
dash.workflow.comments1Science Serial ID 89350
dc.identifier.doi10.1073/pnas.162346699
dash.source.volume99;17
dash.source.page11073


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