Xu Ze, Dai Jieyu, Kang Tongyang, Shah Kamran, Li Qin, Liu Kun, Xing Libo, Ma Juanjuan, Zhang Dong, Zhao Caiping
College of Horticulture, Northwest Agriculture and Forestry University, Yangling, China.
Front Plant Sci. 2022 Mar 25;13:844055. doi: 10.3389/fpls.2022.844055. eCollection 2022.
Pectin is the major component in the primary cell wall and middle lamella, maintaining the physical stability and mechanical strength of the cell wall. Pectate lyase (PL), a cell wall modification enzyme, has a major influence on the structure of pectin. However, little information and no comprehensive analysis is available on the PL gene family in peach ( L. Batsch). In this study, 20 genes were identified in peach. We characterized their physicochemical characteristics, sequence alignments, chromosomal locations, and gene structures. The PpePL family members were classified into five groups based on their phylogenetic relationships. Among those, and had the higher expression abundance in ripe fruit, and and were upregulated during storage. Detailed RT-qPCR analysis revealed that and were responsive to ETH treatment (1 g L ethephon) with an abundant transcript accumulation, which suggested these genes were involved in peach ripening and softening. In addition, virus-induced gene silencing (VIGS) technology was used to identify the roles of and . Compared to controls, the RNAi fruit maintained greater firmness in the early storage stage, increased acid-soluble pectin (ASP), and reduced water-soluble pectin (WSP). Moreover, transmission electron microscopy (TEM) showed that cell wall degradation was reduced in the fruit of RNAi-1 and RNAi-15, which indicated that softening of the RNAi fruit has been delayed. Our results indicated that and play an important role in peach softening by depolymerizing pectin and degrading cell wall.
果胶是植物初生细胞壁和胞间层的主要成分,维持着细胞壁的物理稳定性和机械强度。果胶裂解酶(PL)作为一种细胞壁修饰酶,对果胶结构有重要影响。然而,关于桃(蔷薇科桃属)PL基因家族的信息较少,且尚无全面分析。本研究在桃中鉴定出20个PL基因。我们对其理化特性、序列比对、染色体定位和基因结构进行了表征。基于系统发育关系,桃PpePL家族成员被分为五组。其中,PpePL1和PpePL5在成熟果实中表达丰度较高,PpePL10和PpePL15在贮藏期间上调。详细的RT-qPCR分析表明,PpePL1和PpePL5对乙烯利处理(1 g·L乙烯利)有响应,转录本大量积累,这表明这些基因参与了桃的成熟和软化过程。此外,利用病毒诱导基因沉默(VIGS)技术鉴定了PpePL1和PpePL15的作用。与对照相比,RNA干扰果实在贮藏初期保持了更高的硬度,酸溶性果胶(ASP)增加,水溶性果胶(WSP)减少。此外,透射电子显微镜(TEM)显示,RNA干扰1和RNA干扰15果实的细胞壁降解减少,这表明RNA干扰果实的软化被延迟。我们的结果表明,PpePL1和PpePL15通过使果胶解聚和降解细胞壁在桃软化过程中起重要作用。