Zhang Heng, Zhu Jian-Kang
Department of Genetics and Developmental Science, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Institute of Advanced Biotechnology and School of Medicine, Southern University of Science and Technology, Shenzhen, China.
Nat Rev Mol Cell Biol. 2025 Jan;26(1):51-67. doi: 10.1038/s41580-024-00769-1. Epub 2024 Aug 27.
DNA methylation, also known as 5-methylcytosine, is an epigenetic modification that has crucial functions in plant growth, development and adaptation. The cellular DNA methylation level is tightly regulated by the combined action of DNA methyltransferases and demethylases. Protein complexes involved in the targeting and interpretation of DNA methylation have been identified, revealing intriguing roles of methyl-DNA binding proteins and molecular chaperones. Structural studies and in vitro reconstituted enzymatic systems have provided mechanistic insights into RNA-directed DNA methylation, the main pathway catalysing de novo methylation in plants. A better understanding of the regulatory mechanisms will enable locus-specific manipulation of the DNA methylation status. CRISPR-dCas9-based epigenome editing tools are being developed for this goal. Given that DNA methylation patterns can be stably transmitted through meiosis, and that large phenotypic variations can be contributed by epimutations, epigenome editing holds great promise in crop breeding by creating additional phenotypic variability on the same genetic material.
DNA甲基化,也称为5-甲基胞嘧啶,是一种表观遗传修饰,在植物生长、发育和适应过程中具有关键作用。细胞DNA甲基化水平受到DNA甲基转移酶和去甲基化酶共同作用的严格调控。参与DNA甲基化靶向和解读的蛋白质复合物已被鉴定出来,揭示了甲基DNA结合蛋白和分子伴侣的有趣作用。结构研究和体外重构的酶系统为RNA指导的DNA甲基化提供了机制性见解,这是植物中催化从头甲基化的主要途径。对调控机制的更好理解将实现对DNA甲基化状态的位点特异性操纵。基于CRISPR-dCas9的表观基因组编辑工具正为此目标而开发。鉴于DNA甲基化模式可以通过减数分裂稳定传递,并且表观突变可导致较大的表型变异,表观基因组编辑通过在相同遗传物质上创造额外的表型变异性,在作物育种中具有巨大潜力。