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首页> 外文期刊>Cell cycle >Methylation of human microRNA genes in normal and neoplastic cells.
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Methylation of human microRNA genes in normal and neoplastic cells.

机译:正常和赘生性细胞中人类microRNA基因的甲基化。

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摘要

MicroRNAs (miRNAs) are small RNA molecules that control gene expression by inhibition of protein translation or degradation of cognate target mRNAs. Eventhough strict Even though strict developmental and tissue-specific regulation appears to be critical for miRNA function, very little is known about the mechanisms governing miRNA gene expression. Several recent studies have shown that miRNA genes can regulated DNA methylation and other epigenetic mechanisms. The observation of altered miRNA gene methylation patterns in human cancers also suggested that miRNA gene methylation is functional relevant for tumorigenesis. We have now performed a comprehensive analysis of miRNA genes and found that about half of these genes are associated with CpG islands and thus represent candidate targets of the DNA methylation machinery An expanded analysis of several miRNA-associated CpG islands in five cell lines indicated that miRNA gene methylation is detectable at high frequencies, both in normal and malignant cells.Possible explanations for this phenomenon include the specific structure of miRNA genes and/or their requirement for strict expression regulation.
机译:微小RNA(miRNA)是小的RNA分子,可通过抑制蛋白质翻译或同源靶标mRNA的降解来控制基因表达。尽管严格,即使严格的发育和组织特异性调节对于miRNA功能似乎至关重要,但对于控制miRNA基因表达的机制知之甚少。最近的一些研究表明,miRNA基因可以调节DNA甲基化和其他表观遗传机制。对人类癌症中miRNA基因甲基化模式改变的观察还表明,miRNA基因甲基化在功能上与肿瘤发生有关。现在,我们对miRNA基因进行了全面分析,发现这些基因中约有一半与CpG岛相关,因此代表了DNA甲基化机制的候选靶点。在五个细胞系中对几个与miRNA相关的CpG岛的扩展分析表明,miRNA在正常细胞和恶性细胞中都可以检测到高频率的基因甲基化。对此现象的可能解释包括miRNA基因的特定结构和/或它们对严格表达调控的要求。

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