Correction of PCR-bias in quantitative DNA methylation studies by means of cubic polynomial regression

被引:60
作者
Moskalev, Evgeny A. [1 ]
Zavgorodnij, Mikhail G. [2 ]
Majorova, Svetlana P. [3 ]
Vorobjev, Ivan A. [4 ]
Jandaghi, Pouria [1 ,5 ]
Bure, Irina V. [1 ]
Hoheisel, Jorg D. [1 ]
机构
[1] Deutsch Krebsforschungszentrum, D-69120 Heidelberg, Germany
[2] Voronezh State Univ, Voronezh 394006, Russia
[3] Voronezh State Tech Univ, Voronezh 394026, Russia
[4] Russian Acad Med Sci, Natl Hematol Res Ctr, Moscow 125167, Russia
[5] IAU, Res Ctr Med Sci, Tehran Med Branch, Tehran 193951495, Iran
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; CELL-LINES; BISULFITE; MICROARRAY; EXPRESSION; PATTERNS; PROMOTER; REVEALS; CANCER;
D O I
10.1093/nar/gkr213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation profiling has become an important aspect of biomedical molecular analysis. Polymerase chain reaction (PCR) amplification of bisulphite-treated DNA is a processing step that is common to many currently used methods of quantitative methylation analysis. Preferential amplification of unmethylated alleles-known as PCR-bias-may significantly affect the accuracy of quantification. To date, no universal experimental approach has been reported to overcome the problem. This study presents an effective method of correcting biased methylation data. The procedure includes a calibration performed in parallel to the analysis of the samples under investigation. DNA samples with defined degrees of methylation are analysed. The observed deviation of the experimental results from the expected values is used for calculating a regression curve. The equation of the best-fitting curve is then used for correction of the data obtained from the samples of interest. The process can be applied irrespective of the locus interrogated and the number of sites analysed, avoiding an optimization of the amplification conditions for each individual locus.
引用
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页数:12
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共 32 条
  • [1] High-throughput assessment of CpG site methylation for distinguishing between HCV-cirrhosis and HCV-associated hepatocellular carcinoma
    Archer, Kellie J.
    Mas, Valeria R.
    Maluf, Daniel G.
    Fisher, Robert A.
    [J]. MOLECULAR GENETICS AND GENOMICS, 2010, 283 (04) : 341 - 349
  • [2] Sequence analysis and editing for bisulphite genomic sequencing projects
    Carr, Ian M.
    Valleley, Elizabeth M. A.
    Cordery, Sarah F.
    Markham, Alexander F.
    Bonthron, David T.
    [J]. NUCLEIC ACIDS RESEARCH, 2007, 35 (10)
  • [3] Single-molecule polymerase chain reaction reduces bias: Application to DNA methylation analysis by bisulfite sequencing
    Chhibber, Aparna
    Schroeder, Benjamin G.
    [J]. ANALYTICAL BIOCHEMISTRY, 2008, 377 (01) : 46 - 54
  • [4] Whole Methylome Analysis by Ultra-Deep Sequencing Using Two-Base Encoding
    Chung, Christina A. Bormann
    Boyd, Victoria L.
    McKernan, Kevin J.
    Fu, Yutao
    Monighetti, Cinna
    Peckham, Heather E.
    Barker, Melissa
    [J]. PLOS ONE, 2010, 5 (02):
  • [5] CLARK SJ, 1994, NUCLEIC ACIDS RES, V22, P2990, DOI 10.1093/nar/22.15.2990
  • [6] De novo quantitative bisulfite sequencing using the pyrosequencing technology
    Dupont, JM
    Tost, J
    Jammes, H
    Gut, NG
    [J]. ANALYTICAL BIOCHEMISTRY, 2004, 333 (01) : 119 - 127
  • [7] A GENOMIC SEQUENCING PROTOCOL THAT YIELDS A POSITIVE DISPLAY OF 5-METHYLCYTOSINE RESIDUES IN INDIVIDUAL DNA STRANDS
    FROMMER, M
    MCDONALD, LE
    MILLAR, DS
    COLLIS, CM
    WATT, F
    GRIGG, GW
    MOLLOY, PL
    PAUL, CL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) : 1827 - 1831
  • [8] Genomic screening for genes upregulated by demethylation revealed novel targets of epigenetic silencing in breast cancer
    Fujikane, Tomoko
    Nishikawa, Noriko
    Toyota, Minoru
    Suzuki, Hiromu
    Nojima, Masanori
    Maruyama, Reo
    Ashida, Masami
    Ohe-Toyota, Mutsumi
    Kai, Masahiro
    Nishidate, Toshihiko
    Sasaki, Yasushi
    Ohmura, Tousei
    Hirata, Koichi
    Tokino, Takashi
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2010, 122 (03) : 699 - 710
  • [9] Methylation-specific oligonucleotide microarray: A new potential for high-throughput methylation analysis
    Gitan, RS
    Shi, HD
    Chen, CM
    Yan, PS
    Huang, THM
    [J]. GENOME RESEARCH, 2002, 12 (01) : 158 - 164
  • [10] Microarray technology: beyond transcript profiling and genotype analysis
    Hoheisel, JD
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (03) : 200 - 210