Epigenetic control of the expression of a primate-specific microRNA cluster in human cancer cells

被引:105
|
作者
Tsai, Kuo-Wang [1 ]
Kao, Hsiao-Wei [1 ]
Chen, Hua-Chien [2 ]
Chen, Su-Jen [2 ]
Lin, Wen-chang [1 ,3 ]
机构
[1] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
[2] Chang Gung Univ, Mol Med Res Ctr, Tao Yuan, Taiwan
[3] Natl Yang Ming Univ, Inst Biomed Informat, Taipei 112, Taiwan
关键词
microRNA; C19MC; methylation; CpG island; 5-Aza-dC; REPRESSIVE HISTONE METHYLATION; DNA HYPERMETHYLATION; MOLECULAR EVOLUTION; METHYLTRANSFERASE; IDENTIFICATION; GENES; HMLH1;
D O I
10.4161/epi.4.8.10230
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
Many of the known microRNAs (miRNAs) are encoded by polycistronic transcripts and are thought to be co-expressed. In this study, we discovered that the expression of a large miRNA cluster (C19MC) on human chromosome 19 is upregulated by the demethylating agent, 5-aza-2'-deoxycytidine (5-Aza-dC), in AGS gastric cancer cells. We found that C19MC was rarely expressed in most cells, but its expression was restored through DNA demethylation. We confirmed that this miRNA cluster was mainly expressed in the placenta, as previously reported. Furthermore, its expression pattern was highly correlated with the methylation state of a distal CpG-rich region located about 17.6 kb upstream of the miRNA cluster. Using combined bisulfite restriction analysis (COBRA) and bisulfite-sequencing techniques, we determined that this CpG-rich region is hypermethylated in the AGS and HeLa cells, but hypomethylated in the placenta tissue. In conclusion, we demonstrated that the expression pattern of the C19MC was activated in human cancer cells through demethylation of a CpG-rich region.
引用
收藏
页码:587 / 592
页数:6
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