Cloning of the 5′ upstream region of the rat p16 gene and its role in silencing

被引:22
作者
Abe, M
Okochi, E
Kuramoto, T
Kaneda, A
Takato, T
Sugimura, T
Ushijima, T
机构
[1] Natl Canc Ctr, Res Inst, Div Carcinogenesis, Chuo Ku, Tokyo 1040045, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Oral Surg, Bunkyo Ku, Tokyo 1358655, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2002年 / 93卷 / 10期
关键词
p16; methylation; rat; silencing; CpG islands;
D O I
10.1111/j.1349-7006.2002.tb01211.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypermethylation of the 5' upstream region (5' region) of the human p16(CDKN2A) (p16) gene is known to cause silencing, which is involved in a wide range of human cancers. For the rat p16 gene, its 5' region has not been cloned, and it is uncertain whether surrogate use of exon la is adequate for analysis of p16 silencing. In this study, we observed that methylation analysis of exon la gave false positive results in three samples of normal rat mammary epitheliums and in two of six primary mammary carcinomas. Therefore, we determined the nucleotide sequence of the 5' region of the rat p16 gene. To confirm that methylation status of the 5' region is correlated with p16 expression, the methylation status was analyzed by bisulfite sequencing and methylation-specific PCR in three samples of normal mammary glands, six samples of mammary carcinomas and four cell lines. The 5' region was demethylated in all of the three normal and six carcinoma samples that fully expressed p16. On the other hand, the 5' region was highly methylated in the 3Y1 cell line, which lacked p16 expression, but without deletion. These results showed that the methylation status of the 5' region was more closely correlated with p16 expression than that of the exon W and analysis of the methylation status is useful in examining p16 silencing in various rat tumors.
引用
收藏
页码:1100 / 1106
页数:7
相关论文
共 30 条
[1]  
[Anonymous], MOL CLONING
[2]   DNA hypermethylation in tumorigenesis - epigenetics joins genetics [J].
Baylin, SB ;
Herman, JG .
TRENDS IN GENETICS, 2000, 16 (04) :168-174
[3]   Aberrant methylation of p16INK4a is an early event in lung cancer and a potential biomarker for early diagnosis [J].
Belinsky, SA ;
Nikula, KJ ;
Palmisano, WA ;
Michels, R ;
Saccomanno, G ;
Gabrielson, E ;
Baylin, SB ;
Herman, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11891-11896
[4]   Aberrant CpG island methylation of the p16INK4a and estrogen receptor genes in rat lung tumors induced by particulate carcinogens [J].
Belinsky, SA ;
Snow, SS ;
Nikula, KJ ;
Finch, GL ;
Tellez, CS ;
Palmisano, WA .
CARCINOGENESIS, 2002, 23 (02) :335-339
[5]  
Chan MF, 2000, CURR TOP MICROBIOL, V249, P75
[6]   Alternative models for Carcinogenicity testing: Weight of evidence evaluations across models [J].
Cohen, SM .
TOXICOLOGIC PATHOLOGY, 2001, 29 :183-190
[7]   CPG ISLANDS IN VERTEBRATE GENOMES [J].
GARDINERGARDEN, M ;
FROMMER, M .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 196 (02) :261-282
[8]  
GONZALEZZULUETA M, 1995, CANCER RES, V55, P4531
[9]  
Gonzalgo ML, 1998, CANCER RES, V58, P1245
[10]   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