Rothkegel Karin, Espinoza Alonso, Sanhueza Dayan, Lillo-Carmona Victoria, Riveros Aníbal, Campos-Vargas Reinaldo, Meneses Claudio
Facultad Ciencias de la Vida, Centro de Biotecnología Vegetal, Universidad Andrés Bello, Santiago, Chile.
Departamento de Producción Agrícola, Facultad de Ciencias Agronómicas, Centro de Estudios Postcosecha, Universidad de Chile, Santiago, Chile.
Front Plant Sci. 2021 Jun 10;12:684130. doi: 10.3389/fpls.2021.684130. eCollection 2021.
Peach () fruits have a fast ripening process and a shelf-life of days, presenting a challenge for long-distance consuming markets. To prolong shelf-life, peach fruits are stored at low temperatures (0 to 7 °C) for at least two weeks, which can lead to the development of mealiness, a physiological disorder that reduces fruit quality and decreases consumer acceptance. Several studies have been made to understand this disorder, however, the molecular mechanisms underlying mealiness are not fully understood. Epigenetic factors, such as DNA methylation, modulate gene expression according to the genetic background and environmental conditions. In this sense, the aim of this work was to identify differentially methylated regions (DMRs) that could affect gene expression in contrasting individuals for mealiness. Peach flesh was studied at harvest time (E1 stage) and after cold storage (E3 stage) for 30 days. The distribution of DNA methylations within the eight chromosomes of showed higher methylation levels in pericentromeric regions and most differences between mealy and normal fruits were at Chr1, Chr4, and Chr8. Notably, differences in Chr4 co-localized with previous QTLs associated with mealiness. Additionally, the number of DMRs was higher in CHH cytosines of normal and mealy fruits at E3; however, most DMRs were attributed to mealy fruits from E1, increasing at E3. From RNA-Seq data, we observed that differentially expressed genes (DEGs) between normal and mealy fruits were associated with ethylene signaling, cell wall modification, lipid metabolism, oxidative stress and iron homeostasis. When integrating the annotation of DMRs and DEGs, we identified a and an gene that were downregulated and hypermethylated in mealy fruits, coinciding with the co-localization of a transposable element (TE). Altogether, this study indicates that genetic differences between tolerant and susceptible individuals is predominantly affecting epigenetic regulation over gene expression, which could contribute to a metabolic alteration from earlier stages of development, resulting in mealiness at later stages. Finally, this epigenetic mark should be further studied for the development of new molecular tools in support of breeding programs.
桃()果实成熟过程迅速,货架期仅几天,这给远距离消费市场带来了挑战。为延长货架期,桃果实需在低温(0至7°C)下储存至少两周,这可能导致粉质化,这是一种生理紊乱现象,会降低果实品质并减少消费者接受度。已经开展了多项研究来了解这种紊乱现象,然而,导致粉质化的分子机制尚未完全明确。表观遗传因素,如DNA甲基化,会根据遗传背景和环境条件调节基因表达。从这个意义上讲,本研究的目的是识别可能影响粉质化程度不同的个体中基因表达的差异甲基化区域(DMR)。在收获期(E1阶段)和冷藏30天后(E3阶段)对桃果肉进行了研究。研究表明,在八条染色体上DNA甲基化的分布在着丝粒区域甲基化水平较高,粉质果和正常果之间的大多数差异出现在Chr1、Chr4和Chr8上。值得注意的是,Chr4上的差异与先前与粉质化相关的数量性状位点共定位。此外,在E3阶段,正常果和粉质果的CHH胞嘧啶中DMR的数量较多;然而,大多数DMR来自E1阶段的粉质果,并在E3阶段增加。从RNA测序数据中,我们观察到正常果和粉质果之间差异表达的基因(DEG)与乙烯信号传导、细胞壁修饰、脂质代谢、氧化应激和铁稳态有关。当整合DMR和DEG的注释时,我们鉴定出一个基因和一个基因,它们在粉质果中表达下调且甲基化程度过高,这与一个转座元件(TE)的共定位一致。总之,这项研究表明,耐受性和易感性个体之间的遗传差异主要影响基因表达的表观遗传调控,这可能导致发育早期阶段的代谢改变,从而在后期导致粉质化。最后,这种表观遗传标记应进一步研究,以开发支持育种计划的新分子工具。