DNA甲基化
甲基化
生物
RNA导向的DNA甲基化
小RNA
体育锻炼的表观遗传学
遗传学
CpG站点
甲基转移酶
照明菌甲基化试验
非翻译区
信使核糖核酸
基因
分子生物学
基因表达
出处
期刊:ChemBioChem
[Wiley]
日期:2014-12-02
卷期号:16 (2): 195-203
被引量:78
标识
DOI:10.1002/cbic.201402449
摘要
Abstract miRNAs and DNA methylation are both critical regulators of gene expression. Aberration in miRNA expression or DNA methylation is a causal factor for numerous pathological conditions. DNA methylation can inhibit the transcription of miRNAs, just like coding genes, by methylating the CpG islands in the promoter regions of miRNAs. Conversely, certain miRNAs can directly target DNA methyltransferases and bring about their inhibition, thereby affecting the whole genome methylation pattern. Recently, methylation patterns have also been revealed in mRNA. Surprisingly, the two most commonly studied methylation states in mRNA (m6A and m5C) are found to be enriched in 3′‐UTRs (untranslated regions), the target site for the majority of miRNAs. Whereas m5C is reported to stabilise mRNA, m6A has a destabilising effect on mRNA. However, the effect of mRNA methylation on its interaction with miRNAs is largely unexplored. The review highlights the complex interplay between microRNA and methylation at DNA and mRNA level.
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