Jha Ashwani, Shankar Ravi
Studio of Computational Biology and Bioinformatics, Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology (CSIR-IHBT), Palampur 176 061, India.
J Biosci. 2014 Jun;39(3):365-80. doi: 10.1007/s12038-014-9437-9.
DNA methylation is a type of epigenetic modification where a methyl group is added to the cytosine or adenine residue of a given DNA sequence. It has been observed that DNA methylation is achieved by some collaborative agglomeration of certain proteins and non-coding RNAs. The assembly of IDN2 and its homologous proteins with siRNAs recruits the enzyme DRM2, which adds a methyl group at certain cytosine residues within the DNA sequence. In this study, it was found that de novo DNA methylation might be regulated by miRNAs through systematic targeting of the genes involved in DNA methylation. A comprehensive genome-wide and system-level study of miRNA targeting, transcription factors, DNA-methylation-causing genes and their target genes has provided a clear picture of an interconnected relationship of all these factors which regulate DNA methylation in Arabidopsis. The study has identified a DNA methylation system that is controlled by four different genes: IDN2, IDNl1, IDNl2 and DRM2. These four genes along with various critical transcription factors appear to be controlled by five different miRNAs. Altogether, DNA methylation appears to be a finely tuned process of opposite control systems of DNAmethylation- causing genes and certain miRNAs pitted against each other.
DNA甲基化是一种表观遗传修饰,其中甲基基团被添加到特定DNA序列的胞嘧啶或腺嘌呤残基上。据观察,DNA甲基化是通过某些蛋白质和非编码RNA的协同聚集来实现的。IDN2及其同源蛋白与小干扰RNA(siRNA)的组装招募了DRM2酶,该酶在DNA序列中的某些胞嘧啶残基处添加甲基基团。在这项研究中,发现DNA从头甲基化可能受微小RNA(miRNA)通过对参与DNA甲基化的基因进行系统性靶向调控。一项关于miRNA靶向、转录因子、导致DNA甲基化的基因及其靶基因的全基因组和系统水平的综合研究,清晰地呈现了拟南芥中所有这些调控DNA甲基化的因素之间的相互联系。该研究确定了一个由四个不同基因控制的DNA甲基化系统:IDN2、IDNl1、IDNl2和DRM2。这四个基因以及各种关键转录因子似乎受五种不同的miRNA控制。总之,DNA甲基化似乎是一个由导致DNA甲基化的基因和某些相互对抗的miRNA组成的相反控制系统进行精细调控的过程。