Literature DB >> 9267808

Fidelity and mutational spectrum of Pfu DNA polymerase on a human mitochondrial DNA sequence.

P André1, A Kim, K Khrapko, W G Thilly.   

Abstract

The study of rare genetic changes in human tissues requires specialized techniques. Point mutations at fractions at or below 10(-6) must be observed to discover even the most prominent features of the point mutational spectrum. PCR permits the increase in number of mutant copies but does so at the expense of creating many additional mutations or "PCR noise". Thus, each DNA sequence studied must be characterized with regard to the DNA polymerase and conditions used to avoid interpreting a PCR-generated mutation as one arising in human tissue. The thermostable DNA polymerase derived from Pyrococcus furiosus designated Pfu has the highest fidelity of any DNA thermostable polymerase studied to date, and this property recommends it for analyses of tissue mutational spectra. Here, we apply constant denaturant capillary electrophoresis (CDCE) to separate and isolate the products of DNA amplification. This new strategy permitted direct enumeration and identification of point mutations created by Pfu DNA polymerase in a 96-bp low melting domain of a human mitochondrial sequence despite the very low mutant fractions generated in the PCR process. This sequence, containing part of the tRNA glycine and NADH dehydrogenase subunit 3 genes, is the target of our studies of mitochondrial mutagenesis in human cells and tissues. Incorrectly synthesized sequences were separated from the wild type as mutant/wild-type heteroduplexes by sequential enrichment on CDCE. An artificially constructed mutant was used as an internal standard to permit calculation of the mutant fraction. Our study found that the average error rate (mutations per base pair duplication) of Pfu was 6.5 x 10(-7), and five of its more frequent mutations (hot spots) consisted of three transversions (GC-->TA, AT-->TA, and AT-->CG), one transition (AT-->GC), and one 1-bp deletion (in an AAAAAA sequence). To achieve an even higher sensitivity, the amount of Pfu-induced mutants must be reduced.

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Year:  1997        PMID: 9267808      PMCID: PMC310667          DOI: 10.1101/gr.7.8.843

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  46 in total

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Authors:  M L Michaels; J H Miller
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2.  Transient mutators: a semiquantitative analysis of the influence of translation and transcription errors on mutation rates.

Authors:  J Ninio
Journal:  Genetics       Date:  1991-11       Impact factor: 4.562

3.  Connections between translation, transcription and replication error-rates.

Authors:  J Ninio
Journal:  Biochimie       Date:  1991-12       Impact factor: 4.079

4.  Optimization of the polymerase chain reaction with regard to fidelity: modified T7, Taq, and vent DNA polymerases.

Authors:  L L Ling; P Keohavong; C Dias; W G Thilly
Journal:  PCR Methods Appl       Date:  1991-08

Review 5.  DNA polymerase fidelity and the polymerase chain reaction.

Authors:  K A Eckert; T A Kunkel
Journal:  PCR Methods Appl       Date:  1991-08

6.  The fidelity of Taq polymerase catalyzing PCR is improved by an N-terminal deletion.

Authors:  W M Barnes
Journal:  Gene       Date:  1992-03-01       Impact factor: 3.688

Review 7.  Mutational analysis using denaturing gradient gel electrophoresis and PCR.

Authors:  N F Cariello; T R Skopek
Journal:  Mutat Res       Date:  1993-07       Impact factor: 2.433

8.  Predominant mutations induced by the Thermococcus litoralis, vent DNA polymerase during DNA amplification in vitro.

Authors:  P Keohavong; L Ling; C Dias; W G Thilly
Journal:  PCR Methods Appl       Date:  1993-05

9.  High-fidelity amplification using a thermostable DNA polymerase isolated from Pyrococcus furiosus.

Authors:  K S Lundberg; D D Shoemaker; M W Adams; J M Short; J A Sorge; E J Mathur
Journal:  Gene       Date:  1991-12-01       Impact factor: 3.688

10.  MutT protein specifically hydrolyses a potent mutagenic substrate for DNA synthesis.

Authors:  H Maki; M Sekiguchi
Journal:  Nature       Date:  1992-01-16       Impact factor: 49.962

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  21 in total

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2.  Novel amplification of DNA in a hairpin structure: towards a radical elimination of PCR errors from amplified DNA.

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Journal:  Nucleic Acids Res       Date:  2003-03-15       Impact factor: 16.971

3.  A simple, rapid, high-fidelity and cost-effective PCR-based two-step DNA synthesis method for long gene sequences.

Authors:  Ai-Sheng Xiong; Quan-Hong Yao; Ri-He Peng; Xian Li; Hui-Qin Fan; Zong-Ming Cheng; Yi Li
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4.  Assessing the fidelity of ancient DNA sequences amplified from nuclear genes.

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Journal:  Genetics       Date:  2005-11-19       Impact factor: 4.562

5.  A-to-G hypermutation in the genome of lymphocytic choriomeningitis virus.

Authors:  Roland C Zahn; Ina Schelp; Olaf Utermöhlen; Dorothee von Laer
Journal:  J Virol       Date:  2006-10-04       Impact factor: 5.103

6.  Analysis of mutational spectra by denaturing capillary electrophoresis.

Authors:  Per O Ekstrøm; Konstantin Khrapko; Xiao-Cheng Li-Sucholeiki; Ian W Hunter; William G Thilly
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

Review 7.  Isothermal DNA amplification in vitro: the helicase-dependent amplification system.

Authors:  Yong-Joo Jeong; Kkothanahreum Park; Dong-Eun Kim
Journal:  Cell Mol Life Sci       Date:  2009-07-24       Impact factor: 9.261

8.  Effect of bottlenecking on evolution of the nonstructural protein 3 gene of hepatitis C virus during sexually transmitted acute resolving infection.

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Journal:  J Virol       Date:  2005-12       Impact factor: 5.103

9.  Mitochondrial mutational spectra in human cells and tissues.

Authors:  K Khrapko; H A Coller; P C André; X C Li; J S Hanekamp; W G Thilly
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

10.  Accurate DNA synthesis by Sulfolobus solfataricus DNA polymerase B1 at high temperature.

Authors:  Likui Zhang; Huiqiang Lou; Li Guo; Zhengyan Zhan; Zhenhong Duan; Xin Guo; Li Huang
Journal:  Extremophiles       Date:  2009-12-11       Impact factor: 2.395

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