Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations

被引:54
作者
Kraytsberg, Y
Khrapko, K
机构
[1] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
关键词
aging; allelic; preference; jumping PCR; mitochondrial DNA; mutational spectra; PCR errors; single-molecule PCR; somatic mutations; recombination;
D O I
10.1586/14737159.5.5.809
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A critical review of the clone-by-clone approach to the analysis of complex spectra of somatic mutations is presented. The study of a priori unknown somatic mutations requires painstaking analysis of complex mixtures of multiple mutant and non-mutant DNA molecules. If mutant fractions are sufficiently high, these mixtures can be dissected by the cloning of individual DNA molecules and scanning of the individual clones for mutations (e.g., by sequencing). Currently, the majority of such cloning is performed using PCR fragments. However, post-PCR cloning may result in various PCR artifacts - PCR errors and jumping PCR - and preferential amplification of certain mutations. This review argues that single-molecule PCR is a simple alternative that promises to evade the disadvantages inherent to post-PCR cloning and enhance mutational analysis in the future.
引用
收藏
页码:809 / 815
页数:7
相关论文
共 35 条
  • [1] HPRT mutations in humans:: biomarkers for mechanistic studies
    Albertini, RJ
    [J]. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2001, 489 (01) : 1 - 16
  • [2] A LIFETIME OF RETINAL LIGHT EXPOSURE DOES NOT APPEAR TO INCREASE MITOCHONDRIAL MUTATIONS
    BODENTEICH, A
    MITCHELL, LG
    MERRILL, CR
    [J]. GENE, 1991, 108 (02) : 305 - 309
  • [3] CANTUTICASTELVE.I, 2005, IN PRESS NEUROBIOL A
  • [4] Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication
    Coskun, PE
    Beal, MF
    Wallace, DC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (29) : 10726 - 10731
  • [5] GENETIC STUDIES OF LAC REPRESSOR .4. MUTAGENIC SPECIFICITY IN LACI GENE OF ESCHERICHIA-COLI
    COULONDRE, C
    MILLER, JH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1977, 117 (03) : 577 - 606
  • [6] High mutational burden in the mtDNA control region from aged muscles: a single-fiber study
    Del Bo, R
    Crimi, M
    Sciacco, M
    Malferrari, G
    Bordoni, A
    Napoli, L
    Prelle, A
    Biunno, I
    Moggio, M
    Bresolin, N
    Scarlato, G
    Comi, GP
    [J]. NEUROBIOLOGY OF AGING, 2003, 24 (06) : 829 - 838
  • [7] Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA
    Jazin, EE
    Cavelier, L
    Eriksson, I
    Oreland, L
    Gyllensten, U
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) : 12382 - 12387
  • [8] AMPLIFICATION OF HUMAN MINISATELLITES BY THE POLYMERASE CHAIN-REACTION - TOWARDS DNA FINGERPRINTING OF SINGLE CELLS
    JEFFREYS, AJ
    WILSON, V
    NEUMANN, R
    KEYTE, J
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (23) : 10953 - 10971
  • [9] REPEAT UNIT SEQUENCE VARIATION IN MINISATELLITES - A NOVEL SOURCE OF DNA POLYMORPHISM FOR STUDYING VARIATION AND MUTATION BY SINGLE MOLECULE ANALYSIS
    JEFFREYS, AJ
    NEUMANN, R
    WILSON, V
    [J]. CELL, 1990, 60 (03) : 473 - 485
  • [10] Long-extension PCR to detect deleted mitochondrial DNA molecules is compromised by technical artefacts
    Kajander, OA
    Kunnas, TA
    Perola, M
    Lehtinen, SK
    Karhunen, PJ
    Jacobs, HT
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (02) : 507 - 514