Guangdong Provincial Key Laboratory for Plant Epigenetics, Longhua Bioindustry and Innovation Research Institute, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, Guangdong 518060, China.
Jiangsu Key Laboratory of Genomics, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province 221116, China.
Plant Commun. 2024 Oct 14;5(10):101037. doi: 10.1016/j.xplc.2024.101037. Epub 2024 Jul 6.
N-methyladenosine (mA) is the most abundant modification observed in eukaryotic mRNAs. Advances in transcriptome-wide mA mapping and sequencing technologies have enabled the identification of several conserved motifs in plants, including the RRACH (R = A/G and H = A/C/U) and UGUAW (W = U or A) motifs. However, the mechanisms underlying deposition of mA marks at specific positions in the conserved motifs of individual transcripts remain to be clarified. Evidence from plant and animal studies suggests that mA writer or eraser components are recruited to specific genomic loci through interactions with particular transcription factors, 5-methylcytosine DNA methylation marks, and histone marks. In addition, recent studies in animal cells have shown that microRNAs play a role in depositing mA marks at specific sites in transcripts through a base-pairing mechanism. mA also affects the biogenesis and function of chromatin-associated regulatory RNAs and long noncoding RNAs. Although we have less of an understanding of the link between mA modification and epigenetic factors in plants than in animals, recent progress in identifying the proteins that interact with mA writer or eraser components has provided insights into the crosstalk between mA modification and epigenetic factors, which plays a crucial role in transcript-specific methylation and regulation of mA in plants.
N6-甲基腺苷(m6A)是真核 mRNA 中最丰富的修饰。在全转录组 m6A 图谱和测序技术方面的进步,使得人们能够在植物中鉴定出几个保守的基序,包括 RRACH(R=A/G 和 H=A/C/U)和 UGUAW(W=U 或 A)基序。然而,在单个转录本的保守基序中特定位置沉积 m6A 标记的机制仍有待阐明。来自植物和动物研究的证据表明,m6A 写入器或擦除器组件通过与特定转录因子、5-甲基胞嘧啶 DNA 甲基化标记和组蛋白标记的相互作用,被招募到特定的基因组位点。此外,动物细胞的最近研究表明,miRNA 通过碱基配对机制在转录本的特定位点沉积 m6A 标记。m6A 还影响与染色质相关的调节 RNA 和长非编码 RNA 的生物发生和功能。尽管我们对植物中 m6A 修饰与表观遗传因子之间的联系的了解比对动物中的了解要少,但最近在鉴定与 m6A 写入器或擦除器组件相互作用的蛋白质方面的进展,为 m6A 修饰与表观遗传因子之间的串扰提供了新的见解,这种串扰在植物中转录物特异性甲基化和 m6A 调控中起着至关重要的作用。