Yu Lujia, Sun Yuying, Zhang Xi, Chen Mengchen, Wu Ting, Zhang Jie, Xing Yifan, Tian Ji, Yao Yuncong
Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, Beijing University of Agriculture, Beijing, China.
Department of Plant Science and Technology, Beijing University of Agriculture, Beijing, China.
Hortic Res. 2022 Feb 11;9. doi: 10.1093/hr/uhac007.
Low temperature can affect the growth and development of plants through changes in DNA demethylation patterns. Another known effect of low temperature is the accumulation of anthocyanin pigments. However, it is not known whether the two phenomena are linked, specifically, whether DNA demethylation participates in anthocyanin accumulation in response to low-temperature stress. The ROS1 gene is involved in plant DNA demethylation and influences methylation levels in response to low temperature stress. In this study, using RNA sequencing, we detected that the transcription levels of MdROS1 correlate with the anthocyanin content, as well as with those of anthocyanin biosynthesis-related genes in apple (Malus domestica), at low temperatures. Genomic bisulfite sequencing showed that the methylation levels of the promoters of the anthocyanin related genes MdCHS, MdCHI, MdF3'H, MdANS, MdUFGT, and MdMYB10 decreased in apple leaves after low-temperature treatment. Similar expression and methylation results were also found in apple fruit. Transiently silencing MdROS1 in the leaves and fruit of apple cultivars inhibited the accumulation of anthocyanins and led to decreased expression of anthocyanin biosynthetic genes, and the opposite results were detected in MdROS1-overexpressing leaves and fruit. A promoter binding assay showed that the conserved RRD-DME domains of MdROS1 directly bind to the promoters of MdF3'H and MdUFGT. Taken together, these results suggest that ROS1 affects the anthocyanin biosynthetic pathway by decreasing the methylation level of anthocyanin-related gene promoters, thereby increasing their expression and increasing anthocyanin accumulation.
低温可通过DNA去甲基化模式的变化影响植物的生长发育。低温的另一个已知作用是花青素色素的积累。然而,尚不清楚这两种现象是否相关,具体而言,DNA去甲基化是否参与了低温胁迫下花青素的积累。ROS1基因参与植物DNA去甲基化,并在低温胁迫下影响甲基化水平。在本研究中,我们利用RNA测序检测到,在低温下,苹果(Malus domestica)中MdROS1的转录水平与花青素含量以及花青素生物合成相关基因的转录水平相关。基因组亚硫酸氢盐测序表明,低温处理后苹果叶片中花青素相关基因MdCHS、MdCHI、MdF3'H、MdANS、MdUFGT和MdMYB10启动子的甲基化水平降低。在苹果果实中也发现了类似的表达和甲基化结果。在苹果品种的叶片和果实中瞬时沉默MdROS1抑制了花青素的积累,并导致花青素生物合成基因的表达降低,而在MdROS1过表达的叶片和果实中检测到相反的结果。启动子结合试验表明,MdROS1保守的RRD-DME结构域直接与MdF3'H和MdUFGT的启动子结合。综上所述,这些结果表明,ROS1通过降低花青素相关基因启动子的甲基化水平来影响花青素生物合成途径,从而增加其表达并促进花青素积累。