Bouillon Pierre, Belin Etienne, Fanciullino Anne-Laure, Balzergue Sandrine, Hanteville Sylvain, Letekoma Yao, Cournol Maryline, Faris Fatima, Bouanich Andréa, Bréard Dimitri, Bernard Frédéric, Celton Jean-Marc
Univ Angers, Institut Agro, INRAE, IRHS, SFR QUASAV, Angers, France.
IFO, Seiches sur le Loir, France.
Front Plant Sci. 2025 Jan 13;15:1462545. doi: 10.3389/fpls.2024.1462545. eCollection 2024.
The genetic basis of type 1 red-flesh color development in apple () depends upon a particular allele of the gene. Interestingly, type 1 red-flesh apples are fully red after fruit set, but anthocyanin pigmentation in apple fruit cortex may decrease during fruit growth and maturation, leading to variable red patterning and intensities in the mature cortical flesh. We developed a histogram-based color analysis method to quantitatively estimate pigmentation patterns. This methodology was applied to investigate the phenotypic diversity in four hybrid F1 families segregating for red-flesh color. Pigmentation patterns were found to be heritable allowing the identification of a new locus by QTL analysis. To further investigate the mechanisms involved in the spatial deposition of anthocyanin, metabolome, transcriptome and methylome comparisons between white and red flesh areas within the red-flesh genotype cv. 'R201' exhibiting flesh pigmentation patterns, was performed. Wide-targeted analysis showed that white-flesh areas accumulate more dihydrochalcones and hydroxycinnamic acids than red-flesh areas while red-flesh areas accumulate more flavonoids. Anthocyanin biosynthesis genes and anthocyanin positive regulators (MBW complex) were up-regulated in red-flesh areas, while a reduction in anthocyanin storage, transport and stability (increase of pH, down-regulation of ) and an increase in phenolic catabolism were concomitant with color fading process in white-flesh areas. Expression of was linked to a differentially methylated region (DMR) suggesting a potential environmental effect on the epigenetic control of gene expression involved in color fading. Altogether, these results provide the first characterization and functional identification of color fading in apple fruit flesh.
苹果1型红肉颜色发育的遗传基础取决于基因的一个特定等位基因。有趣的是,1型红肉苹果在坐果后完全呈红色,但苹果果实皮层中的花青素色素沉着在果实生长和成熟过程中可能会减少,导致成熟皮层果肉中出现不同的红色图案和强度。我们开发了一种基于直方图的颜色分析方法来定量估计色素沉着模式。该方法被应用于研究四个红肉颜色分离的杂交F1家系的表型多样性。发现色素沉着模式是可遗传的,从而通过QTL分析鉴定出一个新位点。为了进一步研究花青素空间沉积所涉及的机制,对表现出果肉色素沉着模式的红肉基因型‘R201’的白色和红色果肉区域进行了代谢组、转录组和甲基化组比较。广泛靶向分析表明,白色果肉区域比红色果肉区域积累更多的二氢查耳酮和羟基肉桂酸,而红色果肉区域积累更多的类黄酮。花青素生物合成基因和花青素正调控因子(MBW复合体)在红色果肉区域上调,而白色果肉区域花青素储存、运输和稳定性的降低(pH值升高、下调)以及酚类物质分解代谢的增加与颜色褪色过程相伴。的表达与一个差异甲基化区域(DMR)相关,表明环境可能对参与颜色褪色的基因表达的表观遗传控制产生影响。总之,这些结果首次对苹果果肉颜色褪色进行了表征和功能鉴定。