Wu Shan, Sun Miao, Lian Huashan
School of Landscape Architecture, Chengdu Agricultural College, Wenjiang, China.
Front Plant Sci. 2025 Jun 10;16:1530531. doi: 10.3389/fpls.2025.1530531. eCollection 2025.
Enzymatic browning significantly affects the edible, nutritional, and commercial value of luffa. Investigating the expression and regulation of key enzyme genes involved in the browning process is crucial for understanding the molecular mechanisms underlying luffa browning.
Fruit samples were collected at 15 (S1), 20 (S2), and 45 days (S3) after flowering from two contrasting luffa varieties: the browning-sensitive Long-quan-yi (LQY) and the browning-tolerant Jiang-du (JD). RNA-sequencing technology, combined with ultra-performance liquid chromatography electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS), was used to obtain transcriptome and metabolome data, which were subsequently analyzed using a series of bioinformatics approaches. Quantitative polymerase chain reaction (q-PCR) was used to validate gene expression.
Compared with JD, the ROS levels and PPO activity were elevated in LQY. In the polyphenol metabolic pathway, 24 key enzyme genes including , , and , were identified. In the flavonoid metabolic pathway, 57 key structural genes, such as , , and , were identified. These genes showed different expression patterns between the two luffa varieties. Differentially expressed genes were mainly involved in the regulation of 34 MYB, 15 bHLH, 19 WD40, and 14 WRKY transcription factors. Further metabolomics analysis showed that the levels of polyphenol metabolites were upregulated in LQY, whereas the levels of flavonoid metabolites were upregulated in JD.
This study integrated transcriptomic and metabolomics data to identify key genes, transcription factors and metabolic pathways associated with luffa browning. q-PCR analysis was performed to validate the expression of and genes. These findings provide a theoretical foundation for further investigation into the molecular mechanisms underlying luffa browning and offer potential targets for genetic improvement or breeding strategies to enhance luffa quality.
酶促褐变显著影响丝瓜的食用价值、营养价值和商业价值。研究参与褐变过程的关键酶基因的表达和调控对于理解丝瓜褐变的分子机制至关重要。
从两个对比鲜明的丝瓜品种——对褐变敏感的龙泉一号(LQY)和耐褐变的江都(JD)——开花后15天(S1)、20天(S2)和45天(S3)采集果实样本。采用RNA测序技术,结合超高效液相色谱电喷雾电离串联质谱(UPLC-ESI-MS/MS),获取转录组和代谢组数据,随后使用一系列生物信息学方法进行分析。采用定量聚合酶链反应(q-PCR)验证基因表达。
与JD相比,LQY中的活性氧水平和多酚氧化酶活性升高。在多酚代谢途径中,鉴定出包括 、 和 等在内的24个关键酶基因。在类黄酮代谢途径中,鉴定出57个关键结构基因,如 、 和 等。这些基因在两个丝瓜品种间表现出不同的表达模式。差异表达基因主要参与34个MYB、15个bHLH、19个WD40和14个WRKY转录因子的调控。进一步的代谢组学分析表明,LQY中多酚代谢物水平上调,而JD中类黄酮代谢物水平上调。
本研究整合转录组和代谢组数据,以鉴定与丝瓜褐变相关的关键基因、转录因子和代谢途径。进行q-PCR分析以验证 和 基因的表达。这些发现为进一步研究丝瓜褐变的分子机制提供了理论基础,并为提高丝瓜品质的遗传改良或育种策略提供了潜在靶点。