果实成熟过程中的细胞壁多糖比较分析和转录组轮廓分析揭示了桃肉腻的分子基础

Hongmei Wang, Ang Li, Wenfang Zeng, Zhenyu Yao, Akhi Badrunnesa, Junren Meng, Yule Miao, Liang Niu, Lei Pan, Guochao Cui, Wenyi Duan, Shihang Sun, Guohuai Li, Zhiqiang Wang
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引用次数: 0

摘要

肉质桃干而无味,降低了消费者对其的接受度。更深入地了解脆度的内在机理对于提高桃子的品质至关重要。本研究对 CP13、CP14、CM 和 RM 桃子进行了比较分析。感官评估结果表明,CP13 和 CM 分别属于无粉蚧的粘石桃子和小石桃子,而 CP14 和 RM 则属于粉蚧小石桃子。CP13 和 CP14 被认定为石质硬(SH)桃,在成熟过程中释放的乙烯极少,而 CM 和 RM 被认定为融肉(MF)桃,在成熟过程中释放大量乙烯。扫描电子显微镜(SEM)显微结构观察表明,CP14(SH)和 RM(MF)蚧壳桃果肉组织细胞完整且分离,细胞间距大且排列不规则。果胶新陈代谢的差异影响细胞壁的组成,是导致 "褐变 "的主要因素。蚧壳桃和非蚧壳桃之间聚半乳糖醛酸酶(PG)和果胶甲基酯酶(PME)活性的波动是导致蚧壳的主要因素。然而,导致这些波动的细胞壁代谢变化并没有明确的方向。通过转录组分析和加权基因共表达网络分析(WGCNA),我们确定了 40 个与蚧壳病模式相关的差异表达基因(DEGs)。在这些差异表达基因中,与非蚧壳病桃(CP13 和 CM)相比,编码 PG 的基因在蚧壳病桃(CP14 和 RM)中明显上调。PpPG1 是导致桃嗜粉的主要效应基因,而 PpPG2、PpEGase2、PpEXP1、PpEXP3、PpAGP2、PpIAA4 和 PpABA2 则被确定为调控桃嗜粉的候选基因。这些发现为理解 "绵软 "桃和 "非绵软 "桃之间的纹理差异提供了坚实的实验基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Cell Wall Polysaccharide Analyses and Transcriptome Profiling during Fruit Ripening Reveal the Molecular Basis of Mealiness in Peach
Mealy peaches are dry and flavorless, which reduces their consumer acceptance. A deeper understanding of the mechanism underlying mealiness is crucial to enhancing peach fruit quality. In this study, comparative profiling was conducted on CP13, CP14, CM, and RM peaches. Sensory evaluation indicated that CP13 and CM are non-mealy clingstone and freestone peaches, respectively, and CP14 and RM are mealy freestone peaches. Both CP13 and CP14, identified as stony hard (SH) peaches, exhibited minimal ethylene release, whereas CM and RM, identified as melting flesh (MF) peaches, released high amounts of ethylene during the ripening process. Scanning electron microscopy (SEM) microstructure observation indicated that cells in the flesh tissue of mealy peaches, CP14 (SH) and RM (MF), were intact and separated, with large intercellular spaces and irregular arrangements. The main factor that promotes mealiness is differences in pectin metabolism, which impact cell wall composition. The fluctuations in polygalacturonase (PG) and pectin methylesterase (PME) activity between mealy and non-mealy peaches were the main factor contributing to mealiness. However, the changes in cell wall metabolism that caused these fluctuations did not have a clear direction. Using transcriptome analysis and weighted gene co-expression network analysis (WGCNA), we were able to identify forty differentially expressed genes (DEGs) that are associated with mealy patterns. Among these DEGs, genes encoding PG were significantly upregulated in mealy peaches (CP14 and RM) compared to non-mealy peaches (CP13 and CM). PpPG1 was the main effector gene for mealiness, while PpPG2, PpEGase2, PpEXP1, PpEXP3, PpAGP2, PpIAA4, and PpABA2 were identified as candidate genes regulating peach mealiness. These findings provide a solid experimental basis for understanding the textual distinctions between mealy and non-mealy peaches.
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