Li Hui-Liang, Wang Ying, Guo Dong, Zhu Jia-Hong, Wang Yu, Dai Hao-Fu, Peng Shi-Qing
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences and Key Laboratory for Biology and Genetic Resources of Hainan Province, Hainan Academy of Tropical Agricultural Resource, Haikou, Hainan, China.
National Key Laboratory for Tropical Crop Breeding and Sanya Research Institute, Chinese Academy of Tropical Agricultural Sciences, Sanya, Hainan, China.
Front Plant Sci. 2024 Jun 24;15:1407700. doi: 10.3389/fpls.2024.1407700. eCollection 2024.
Rubber tree () is reproduced by bud grafting for commercial planting, but significant intraclonal variations exist in bud-grafted clones. DNA methylation changes related to grafting may be partly responsible for intraclonal variations. In the current study, whole-genome DNA methylation profiles of grafted rubber tree plants (GPs) and their donor plants (DPs) were evaluated by whole-genome bisulfite sequencing. Data showed that DNA methylation was downregulated and DNA methylations in CG, CHG, and CHH sequences were reprogrammed in GPs, suggesting that grafting induced the reprogramming of DNA methylation. A total of 5,939 differentially methylated genes (DMGs) were identified by comparing fractional methylation levels between GPs and DPs. Transcriptional analysis revealed that there were 9,798 differentially expressed genes (DEGs) in the DP and GP comparison. A total of 1,698 overlapping genes between DEGs and DMGs were identified. These overlapping genes were markedly enriched in the metabolic pathway and biosynthesis of secondary metabolites by Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Global DNA methylation and transcriptional analyses revealed that reprogramming of DNA methylation is correlated with gene expression in grafted rubber trees. The study provides a whole-genome methylome of rubber trees and an insight into the molecular mechanisms underlying the intraclonal variations existing in the commercial planting of grafted rubber trees.
橡胶树()通过芽接进行繁殖以用于商业种植,但芽接克隆中存在显著的克隆内变异。与嫁接相关的DNA甲基化变化可能部分导致了克隆内变异。在本研究中,通过全基因组亚硫酸氢盐测序评估了嫁接橡胶树植株(GPs)及其供体植株(DPs)的全基因组DNA甲基化图谱。数据显示,GPs中DNA甲基化下调,CG、CHG和CHH序列中的DNA甲基化被重新编程,这表明嫁接诱导了DNA甲基化的重新编程。通过比较GPs和DPs之间的甲基化分数水平,共鉴定出5939个差异甲基化基因(DMGs)。转录分析显示,在DP和GP的比较中有9798个差异表达基因(DEGs)。在DEGs和DMGs之间共鉴定出1698个重叠基因。通过京都基因与基因组百科全书(KEGG)通路分析,这些重叠基因在代谢途径和次生代谢物生物合成中显著富集。全基因组DNA甲基化和转录分析表明,DNA甲基化的重新编程与嫁接橡胶树中的基因表达相关。该研究提供了橡胶树的全基因组甲基化图谱,并深入了解了嫁接橡胶树商业种植中存在的克隆内变异的分子机制。