Chen Weiwei, Kong Junhua, Qin Cheng, Yu Sheng, Tan Jinjuan, Chen Yun-ru, Wu Chaoqun, Wang Hui, Shi Yan, Li Chunyang, Li Bin, Zhang Pengcheng, Wang Ying, Lai Tongfei, Yu Zhiming, Zhang Xian, Shi Nongnong, Wang Huizhong, Osman Toba, Liu Yule, Manning Kenneth, Jackson Stephen, Rolin Dominique, Zhong Silin, Seymour Graham B, Gallusci Philippe, Hong Yiguo
Research Centre for Plant RNA Signalling, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China.
State Key Laboratory of Agrobiotechnology, School of Life Sciences, The Chinese University of Hong Kong, Hong Kong.
Sci Rep. 2015 Mar 17;5:9192. doi: 10.1038/srep09192.
Naturally-occurring epimutants are rare and have mainly been described in plants. However how these mutants maintain their epigenetic marks and how they are inherited remain unknown. Here we report that CHROMOMETHYLASE3 (SlCMT3) and other methyltransferases are required for maintenance of a spontaneous epimutation and its cognate Colourless non-ripening (Cnr) phenotype in tomato. We screened a series of DNA methylation-related genes that could rescue the hypermethylated Cnr mutant. Silencing of the developmentally-regulated SlCMT3 gene results in increased expression of LeSPL-CNR, the gene encodes the SBP-box transcription factor residing at the Cnr locus and triggers Cnr fruits to ripen normally. Expression of other key ripening-genes was also up-regulated. Targeted and whole-genome bisulfite sequencing showed that the induced ripening of Cnr fruits is associated with reduction of methylation at CHG sites in a 286-bp region of the LeSPL-CNR promoter, and a decrease of DNA methylation in differentially-methylated regions associated with the LeMADS-RIN binding sites. Our results indicate that there is likely a concerted effect of different methyltransferases at the Cnr locus and the plant-specific SlCMT3 is essential for sustaining Cnr epi-allele. Maintenance of DNA methylation dynamics is critical for the somatic stability of Cnr epimutation and for the inheritance of tomato non-ripening phenotype.
自然发生的表观突变体很罕见,主要在植物中被描述过。然而,这些突变体如何维持其表观遗传标记以及如何遗传仍然未知。在这里,我们报告说,番茄中维持自发表观突变及其相关的无色不成熟(Cnr)表型需要染色体甲基转移酶3(SlCMT3)和其他甲基转移酶。我们筛选了一系列可以挽救超甲基化Cnr突变体的DNA甲基化相关基因。发育调控的SlCMT3基因沉默导致LeSPL-CNR表达增加,该基因编码位于Cnr位点的SBP-box转录因子,并触发Cnr果实正常成熟。其他关键成熟基因的表达也上调。靶向和全基因组亚硫酸氢盐测序表明,Cnr果实的诱导成熟与LeSPL-CNR启动子286bp区域CHG位点甲基化的减少以及与LeMADS-RIN结合位点相关的差异甲基化区域DNA甲基化的降低有关。我们的结果表明,Cnr位点可能存在不同甲基转移酶的协同作用,植物特异性的SlCMT3对于维持Cnr表观等位基因至关重要。DNA甲基化动态的维持对于Cnr表观突变的体细胞稳定性和番茄不成熟表型的遗传至关重要。