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Direct PCR Sequencing with Boronated Nucleotides
Author(s) -
Kenneth Wiggins Porter,
J. D. Briley,
Barbara Ramsay Shaw
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.8.1611
Subject(s) - biology , sequencing by ligation , primer (cosmetics) , exonuclease iii , nucleotide , massive parallel sequencing , dna nanoball sequencing , dna sequencing , polymerase chain reaction , primer dimer , dna , multiple displacement amplification , microbiology and biotechnology , exonuclease , inverse polymerase chain reaction , nucleic acid sequence , sequencing by hybridization , taq polymerase , dna sequencer , genetics , dna polymerase , nested polymerase chain reaction , gene , genomic library , base sequence , multiplex polymerase chain reaction , dna extraction , thermus aquaticus , chemistry , escherichia coli , organic chemistry
A method is described to simultaneously amplify and sequence DNA using a new class of nucleotides containing boron. During the polymerase chain reaction, boron-modified nucleotides, i.e. 2'-deoxynucleoside 5'-alpha-[P-borano]-triphosphates, are incorporated into the product DNA. The boranophosphate linkages are resistant to nucleases and thus the positions of the boranophosphates can be revealed by exonuclease digestion, thereby generating a set of fragments that defines the DNA sequence. The boranophosphate method offers an alternative to current PCR sequencing methods. Single-sided primer extension with dideoxynucleotide chain terminators is avoided, with the consequence that the sequencing fragments are derived directly from the original PCR products. Boranophosphate sequencing is demonstrated with the Pharmacia and the Applied Biosystems 373A automatic sequencers, producing data that is comparable with cycle sequencing.

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