State Key Laboratory of Tree Genetics and Breeding & Key Laboratory of Tree Breeding and Cultivation, National Forestry and Grassland Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing, China.
Non-timber Forestry Research and Development Center, Chinese Academy of Forestry & Key Laboratory of Non-timber Forest Germplasm Enhancement & Utilization of National Forestry and Grassland Administration, Zhengzhou, China.
RNA Biol. 2021 Nov 12;18(sup2):794-803. doi: 10.1080/15476286.2021.1992996. Epub 2021 Nov 21.
In plants, recent studies have revealed that N6-methyladenosine (mA) methylation of mRNA has potential regulatory functions of this mRNA modification in many biological processes. mA methyltransferase, mA demethylase and mA-binding proteins can cause differential phenotypes, indicating that mA may have critical roles in the plant. In this study, we depicted the mA map of sea buckthorn ( Linn.) transcriptome. Similar to , mA sites of sea buckthorn transcriptome is significantly enriched around the stop codon and within 3'-untranslated regions (3'UTR). Gene ontology analysis shows that the mA modification genes are associated with metabolic biosynthesis. In addition, we identified 13,287 different mA peaks (DMPs) between leaf under drought (TR) and control (CK) treatment. It reveals that mA has a high level of conservation and has a positive correlation with mRNA abundance in plants. GO and KEGG enrichment results showed that DMP modification DEGs in TR were particularly associated with ABA biosynthesis. Interestingly, our results showed three mA demethylase ( and ) genes were significantly increased following drought stress, which indicated that it may contributed the decreased mA levels. This exhaustive mA map provides a basis and resource for the further functional study of mRNA mA modification in abiotic stress.
在植物中,最近的研究表明,mRNA 中的 N6-甲基腺苷(m6A)甲基化在许多生物过程中对这种 mRNA 修饰具有潜在的调控功能。m6A 甲基转移酶、m6A 去甲基化酶和 m6A 结合蛋白可引起表型差异,表明 m6A 可能在植物中具有关键作用。在这项研究中,我们描绘了沙棘(Linn.)转录组的 m6A 图谱。与 类似,沙棘转录组的 m6A 位点在终止密码子附近和 3'-非翻译区(3'UTR)内显著富集。GO 分析表明,m6A 修饰基因与代谢生物合成有关。此外,我们在干旱(TR)和对照(CK)处理的叶片之间鉴定出了 13287 个不同的 m6A 峰(DMP)。这表明 m6A 在植物中具有高度的保守性,并且与 mRNA 丰度呈正相关。GO 和 KEGG 富集结果表明,TR 中 DMP 修饰的 DEGs 特别与 ABA 生物合成有关。有趣的是,我们的结果表明,三个 m6A 去甲基化酶(和)基因在干旱胁迫下显著增加,这表明它可能导致 m6A 水平降低。这个详尽的 m6A 图谱为进一步研究非生物胁迫下 mRNA m6A 修饰的功能提供了基础和资源。