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非 CpG 甲基化——癌症中关键的表观遗传修饰。

Non-CpG methylation-a key epigenetic modification in cancer.

出版信息

Brief Funct Genomics. 2021 Sep 11;20(5):304-311. doi: 10.1093/bfgp/elab035.

Abstract

The methylation of cytosine residues that precede adenine/thymine or other cytosine nucleotides instead of guanine in DNA is known as non-CpG methylation. It is a pronounced epigenetic modification with a central role in gene regulation similar to CpG methylation. Due to technological limitations, the locus-specific role of non-CpG methylation was scarcely understood. At present, high-throughput analyses and improved enrichment methods can elucidate the role of genome-wide non-CpG methylation distributions. Although the functional basis of non-CpG methylation in regulating gene expression control is known, its role in cancer development is yet to be ascertained. This review sheds light on the possible mechanism of non-CpG methylation in embryos and developed tissues with a special focus on cancer development and progression. In particular, the maintenance and alteration of non-CpG methylation levels and the crucial factors that determine this level of non-CpG methylation and its functional role in cancer are discussed.

摘要

DNA 中腺嘌呤/胸腺嘧啶或其他胞嘧啶核苷酸前的胞嘧啶残基的甲基化而不是鸟嘌呤的甲基化被称为非 CpG 甲基化。它是一种明显的表观遗传修饰,在基因调控中起着类似于 CpG 甲基化的核心作用。由于技术限制,非 CpG 甲基化的特定基因座作用几乎不为人知。目前,高通量分析和改进的富集方法可以阐明全基因组非 CpG 甲基化分布的作用。尽管非 CpG 甲基化在调节基因表达控制方面的功能基础已为人所知,但它在癌症发展中的作用仍有待确定。本综述重点介绍了非 CpG 甲基化在胚胎和发育组织中的可能机制,特别是非 CpG 甲基化水平的维持和改变,以及决定非 CpG 甲基化水平及其在癌症中的功能作用的关键因素。

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