Sayed Sabrina Bintay, Rabbi Md Afser, Debnath Joy Prokash, Hossen Kabir, Ghosh Ajit
Department of Biochemistry and Molecular Biology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
PLoS One. 2025 Jul 24;20(7):e0328773. doi: 10.1371/journal.pone.0328773. eCollection 2025.
N6-methyladenosine (m6A) is one of the most prevalent mRNA modifications in eukaryotes, playing a crucial role in plant development and stress responses. The m6A modification is regulated by three key components: writers (which add methyl groups), erasers (which remove them), and readers (which interpret the modification). Despite its significance, the role of m6A regulatory genes in plants, particularly in soybean, remains largely unexplored. This study identified 42 m6A regulatory genes in soybean through a comprehensive genome-wide analysis. Structural analysis revealed diverse gene architectures and functional variations across different subgroups. A total of 18 gene duplication events were identified, predominantly evolving under purifying selection. Network analysis and hub gene identification suggested weaker interactions among eraser proteins. Moreover, interaction analysis between miRNAs and soybean m6A regulatory genes indicated a stronger miRNA-mediated regulation of writer components compared to erasers and readers. Expression profiling under various stress conditions highlighted distinct regulatory patterns, where GmECT9, GmECT13, and GmECT17 were highly expressed in roots and nodules, while GmMTB2 and GmALKBH9B2 exhibited maximum upregulation and downregulation, respectively, under combined water deficit and heat stress. Additionally, in the case of mosaic virus infection, GmALKBH9B4 showed significant downregulation, whereas GmMTB1, GmMTB2, and GmALKBH9B1 were upregulated. This study provides a foundational framework for understanding m6A regulatory genes in soybean. The genome-wide insights presented here contribute to a deeper understanding of the molecular mechanisms governing m6A regulation and its potential implications for stress responses and plant development.
N6-甲基腺嘌呤(m6A)是真核生物中最普遍的mRNA修饰之一,在植物发育和应激反应中起关键作用。m6A修饰由三个关键成分调控:写入器(添加甲基基团)、擦除器(去除甲基基团)和读取器(解读修饰)。尽管其具有重要意义,但m6A调控基因在植物中,尤其是在大豆中的作用仍 largely unexplored。本研究通过全面的全基因组分析在大豆中鉴定出42个m6A调控基因。结构分析揭示了不同亚组间多样的基因结构和功能变异。共鉴定出18个基因复制事件,主要在纯化选择下进化。网络分析和枢纽基因鉴定表明擦除器蛋白之间的相互作用较弱。此外,miRNA与大豆m6A调控基因之间的相互作用分析表明,与擦除器和读取器相比,miRNA对写入器成分的调控更强。各种应激条件下的表达谱突出了不同的调控模式,其中GmECT9、GmECT13和GmECT17在根和根瘤中高表达,而GmMTB2和GmALKBH9B2在水分亏缺和热胁迫联合处理下分别表现出最大上调和下调。此外,在花叶病毒感染的情况下,GmALKBH9B4表现出显著下调,而GmMTB1、GmMTB2和GmALKBH9B1上调。本研究为理解大豆中的m6A调控基因提供了一个基础框架。这里呈现的全基因组见解有助于更深入地理解调控m6A的分子机制及其对应激反应和植物发育的潜在影响。