Zhang Xu, Zhu Lijuan, Qian Ming, Jiang Li, Gu Peng, Jia Luting, Qian Chunlu, Luo Weiqi, Ma Min, Wu Zhangfei, Qiao Xin, Wang Libin, Zhang Shaoling
State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing, 210095, Jiangsu, China.
College of Food Science and Technology, Nanjing Agricultural University, Nanjing, 210095, Jiangsu, China.
Mol Hortic. 2024 Feb 20;4(1):6. doi: 10.1186/s43897-024-00081-8.
Putrescine plays a role in superficial scald development during the cold storage of pear fruit. However, the molecular mechanism behind this phenomenon has not been un-fully clarified until recently. In this study, a conjoint analysis of metabolites and gene expression profiles in the putrescine-metabolic pathway of P. bretschneideri Rehd. fruit followed by experimental validation revealed that PbrADC1, forming a homodimer in the chloroplast, was involved in putrescine biosynthesis and thus fruit chilling resistance. Additionally, the substrate-binding residue Cys in PbrADC1, whose activity was modified by HO, played a crucial role in arginine decarboxylation into agmatine. Through a combined analysis of the distribution of cis-acting elements in the PbrADC1 promoter as well as the expression profiles of related transcription factors (TFs), several TFs were identified as upstream regulators of PbrADC1 gene. Further investigation revealed that the nuclear PbrWRKY62 could directly bind to the W-box elements in the PbrADC1 promoter, activate its expression, enhance putrescine accumulation, and thus increase fruit chilling tolerance. In conclusion, our results suggest that the PbrWRKY62-PbrADC1 module is involved in the development of superficial scald in P. bretschneideri Rehd. fruit via regulating putrescine biosynthesis. Consequently, these findings could serve as valuable genetic resources for breeding scald-resistant pear fruit.
腐胺在梨果实冷藏期间的表面烫伤发展中起作用。然而,直到最近,这一现象背后的分子机制仍未完全阐明。在本研究中,对鸭梨果实腐胺代谢途径中的代谢物和基因表达谱进行联合分析,随后通过实验验证发现,在叶绿体中形成同二聚体的PbrADC1参与了腐胺生物合成,进而影响果实的抗冷性。此外,PbrADC1中的底物结合残基Cys的活性受HO修饰,在精氨酸脱羧生成胍丁胺过程中起关键作用。通过对PbrADC1启动子顺式作用元件分布以及相关转录因子(TFs)表达谱的综合分析,鉴定出几个TFs作为PbrADC1基因的上游调控因子。进一步研究发现,细胞核中的PbrWRKY62可直接结合到PbrADC1启动子中的W-box元件上,激活其表达,增强腐胺积累,从而提高果实的耐冷性。总之,我们的结果表明,PbrWRKY62-PbrADC1模块通过调节腐胺生物合成参与鸭梨果实表面烫伤的发展。因此,这些发现可为培育抗烫伤梨品种提供有价值的遗传资源。