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人类癌细胞中灵长类特异性 microRNA 簇表达的表观遗传调控。

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

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.

出版信息

Epigenetics. 2009 Nov 16;4(8):587-92. doi: 10.4161/epi.4.8.10230. Epub 2009 Nov 3.

Abstract

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.

摘要

许多已知的 microRNAs(miRNAs)是由多顺反子转录本编码的,被认为是共表达的。在这项研究中,我们发现人类 19 号染色体上的一个大型 miRNA 簇(C19MC)的表达被去甲基化剂 5-氮杂-2'-脱氧胞苷(5-Aza-dC)上调,在 AGS 胃癌细胞中。我们发现,C19MC 在大多数细胞中很少表达,但通过 DNA 去甲基化可以恢复其表达。我们证实了该 miRNA 簇主要在上皮组织中表达,如先前报道的那样。此外,其表达模式与位于 miRNA 簇上游约 17.6 kb 的远端富含 CpG 区的甲基化状态高度相关。通过联合亚硫酸氢盐限制性分析(COBRA)和亚硫酸氢盐测序技术,我们确定在 AGS 和 HeLa 细胞中,这个富含 CpG 的区域高度甲基化,而在上皮组织中低甲基化。总之,我们证明了 C19MC 的表达模式通过富含 CpG 区域的去甲基化在人类癌细胞中被激活。

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