Bisulfite conversion-specific and methylation-specific PCR: a sensitive technique for accurate evaluation of CpG methylation

被引:54
作者
Sasaki, M
Anast, J
Bassett, W
Kawakami, T
Sakuragi, N
Dahiya, R [1 ]
机构
[1] Univ Calif San Francisco, Dept Urol, San Francisco, CA 94121 USA
[2] Vet Affairs Med Ctr, San Francisco, CA 94121 USA
[3] Hokkaido Univ, Sch Med, Dept Obstet & Gynecol, Kita Ku, Sapporo, Hokkaido 060, Japan
关键词
bisulfite conversion-specific MSP; bisulfite conversion-specific restriction analysis incomplete bisulfite conversion; false-positive; methylation status;
D O I
10.1016/j.bbrc.2003.08.005
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
Methylation-specific PCR (MSP) is frequently used to distinguish methylated alleles in the genome. Sequences that have been incompletely converted during bisulfite treatment are frequently co-amplified during MSP. For accurate MSP, it is important to detect methylated sequences in a background of unconverted DNA with a high level of sensitivity. We report here sensitive techniques, bisulfite conversion-specific MSP (BS-MSP) to accurately evaluate CpG methylation. BS-MSP provides accurate results across a wide spectrum of bisulfite conversion levels. BS-MSP is also confirmed to be a useful technique for the routine analysis of clinical tumor specimens that were paraffin-embedded and microdissected. BS-MSP thus provides the powerful features of ease of use and compatibility with paraffin sections. We recommend that methylation analysis should include a step to eliminate unconverted DNA to avoid overestimation of the DNA methylation level in the samples. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:305 / 309
页数:5
相关论文
共 13 条
[1]   Methylation of the E-cadherin gene in bladder neoplasia and in normal urothelial epithelium from elderly individuals [J].
Bornman, DM ;
Mathew, S ;
Alsruhe, J ;
Herman, JG ;
Gabrielson, E .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (03) :831-835
[2]  
CLARK SJ, 1994, NUCLEIC ACIDS RES, V22, P2990, DOI 10.1093/nar/22.15.2990
[3]   A GENOMIC SEQUENCING PROTOCOL THAT YIELDS A POSITIVE DISPLAY OF 5-METHYLCYTOSINE RESIDUES IN INDIVIDUAL DNA STRANDS [J].
FROMMER, M ;
MCDONALD, LE ;
MILLAR, DS ;
COLLIS, CM ;
WATT, F ;
GRIGG, GW ;
MOLLOY, PL ;
PAUL, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) :1827-1831
[4]  
Grunau C, 2001, Nucleic Acids Res, V29, pE65, DOI 10.1093/nar/29.13.e65
[5]   Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands [J].
Herman, JG ;
Graff, JR ;
Myohanen, S ;
Nelkin, BD ;
Baylin, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9821-9826
[6]   MethPrimer: designing primers for methylation PCRs [J].
Li, LC ;
Dahiya, R .
BIOINFORMATICS, 2002, 18 (11) :1427-1431
[7]   Identifying 5-methylcytosine and related modifications in DNA genomes [J].
Rein, T ;
DePamphilis, ML ;
Zorbas, H .
NUCLEIC ACIDS RESEARCH, 1998, 26 (10) :2255-2264
[8]   CpG hypermethylation of promoter region and inactivation of E-cadherin gene in human bladder cancer [J].
Ribeiro, LA ;
Franks, J ;
Sasaki, M ;
Shiina, H ;
Li, LC ;
Nojima, D ;
Arap, S ;
Carroll, P ;
Enokida, H ;
Nakagawa, M ;
Yonezawa, S ;
Dahiya, R .
MOLECULAR CARCINOGENESIS, 2002, 34 (04) :187-198
[9]  
Sasaki M, 2001, CANCER RES, V61, P97
[10]  
Sasaki M, 2002, J NATL CANCER I, V94, P384