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人类let-7a-3基因座包含一个具有致癌功能的表观遗传调控的微小RNA基因。

The human let-7a-3 locus contains an epigenetically regulated microRNA gene with oncogenic function.

作者信息

Brueckner Bodo, Stresemann Carlo, Kuner Ruprecht, Mund Cora, Musch Tanja, Meister Michael, Sültmann Holger, Lyko Frank

机构信息

Divisions of Epigenetics and Molecular Genome Analysis, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 580, 69120 Heidelberg, Germany.

出版信息

Cancer Res. 2007 Feb 15;67(4):1419-23. doi: 10.1158/0008-5472.CAN-06-4074.

Abstract

MicroRNAs (miRNAs) are small noncoding RNAs that repress their target mRNAs by complementary base pairing and induction of the RNA interference pathway. It has been shown that miRNA expression can be regulated by DNA methylation and it has been suggested that altered miRNA gene methylation might contribute to human tumorigenesis. In this study, we show that the human let-7a-3 gene on chromosome 22q13.31 is associated with a CpG island. Let-7a-3 belongs to the archetypal let-7 miRNA gene family and was found to be methylated by the DNA methyltransferases DNMT1 and DNMT3B. The gene was heavily methylated in normal human tissues but hypomethylated in some lung adenocarcinomas. Let-7a-3 hypomethylation facilitated epigenetic reactivation of the gene and elevated expression of let-7a-3 in a human lung cancer cell line resulted in enhanced tumor phenotypes and oncogenic changes in transcription profiles. Our results thus identify let-7a-3 as an epigenetically regulated miRNA gene with oncogenic function and suggest that aberrant miRNA gene methylation might contribute to the human cancer epigenome.

摘要

微小RNA(miRNA)是一类小的非编码RNA,通过互补碱基配对和诱导RNA干扰途径来抑制其靶mRNA。研究表明,miRNA表达可受DNA甲基化调控,并且有人提出,miRNA基因甲基化改变可能与人类肿瘤发生有关。在本研究中,我们发现位于22q13.31染色体上的人类let-7a-3基因与一个CpG岛相关。Let-7a-3属于典型的let-7 miRNA基因家族,被发现可被DNA甲基转移酶DNMT1和DNMT3B甲基化。该基因在正常人体组织中高度甲基化,但在一些肺腺癌中低甲基化。Let-7a-3低甲基化促进了该基因的表观遗传重新激活,在人肺癌细胞系中let-7a-3表达升高导致肿瘤表型增强和转录谱发生致癌性变化。因此,我们的结果确定let-7a-3是一个具有致癌功能的表观遗传调控的miRNA基因,并表明异常的miRNA基因甲基化可能与人类癌症表观基因组有关。

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