Literature DB >> 15051811

A third base pair for the polymerase chain reaction: inserting isoC and isoG.

Scott C Johnson1, Christopher B Sherrill, David J Marshall, Michael J Moser, James R Prudent.   

Abstract

Two additional bases (isoguanosine and isocytosine), generating a third base pair, have been implemented in PCR. Enzyme fidelity for the third base pair is demonstrated using molecular thermodynamic melting, chemical cleavage and molecular beacons. When amplifying as few as 15 targets containing multiple non-natural base pairs with 40 cycles of amplification, our results confirm sequence conservation. The additional sequence space provided by three base pairs allows for the construction of molecular tools that achieve higher complexity and better discrimination than those possible with natural DNA alone.

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Year:  2004        PMID: 15051811      PMCID: PMC390373          DOI: 10.1093/nar/gkh522

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  21 in total

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4.  Quantitative analysis of receptors for adenosine nucleotides obtained via in vitro selection from a library incorporating a cationic nucleotide analog.

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5.  RNA cleavage by a DNA enzyme with extended chemical functionality.

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7.  An unnatural hydrophobic base pair with shape complementarity between pyrrole-2-carbaldehyde and 9-methylimidazo[(4,5)-b]pyridine.

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8.  Enzymatic repair of an expanded genetic information system.

Authors:  Michael J Moser; James R Prudent
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

9.  Unnatural base pairs for specific transcription.

Authors:  T Ohtsuki; M Kimoto; M Ishikawa; T Mitsui; I Hirao; S Yokoyama
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-24       Impact factor: 11.205

10.  BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping.

Authors:  Arnold Oliphant; David L Barker; John R Stuelpnagel; Mark S Chee
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  28 in total

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2.  Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project.

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Review 3.  Setting the stage: the history, chemistry, and geobiology behind RNA.

Authors:  Steven A Benner; Hyo-Joong Kim; Zunyi Yang
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-01-01       Impact factor: 10.005

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5.  Synthesis and properties of size-expanded DNAs: toward designed, functional genetic systems.

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6.  Polymerase amplification, cloning, and gene expression of benzo-homologous "yDNA" base pairs.

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Review 7.  Nucleic acid-based fluorescent probes and their analytical potential.

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8.  Conversion strategy using an expanded genetic alphabet to assay nucleic acids.

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9.  Tautomeric Equilibria of Nucleobases in the Hachimoji Expanded Genetic Alphabet.

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10.  Expanded genetic alphabets in the polymerase chain reaction.

Authors:  Zunyi Yang; Fei Chen; Stephen G Chamberlin; Steven A Benner
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