Department of Agronomy, National Chung Hsing University, Taichung City 40227, Taiwan.
Department of Horticulture and Biotechnology, Chinese Culture University, Taipei 11114, Taiwan.
Curr Protein Pept Sci. 2024;25(8):651-665. doi: 10.2174/0113892037299818240408053000.
This study investigates the impact of IbACP ( anti-cancer peptide) on defense-related gene expression in tomato leaves, focusing on its role in plant defense mechanisms.
Previously, IbACP was isolated from sweet potato leaves, and it was identified as a peptide capable of inducing an alkalinization response in tomato suspension culture media. Additionally, IbACP was found to regulate the proliferation of human pancreatic adenocarcinoma cells.
Elucidate IbACP's molecular influence on defense-related gene expression in tomato leaves using next-generation sequencing analysis.
To assess the impact of IbACP on defense-related gene expression, transcriptome data were analyzed, encompassing various functional categories such as photosynthesis, metabolic processes, and plant defense. Semi-quantitative reverse-transcription polymerase chain reaction analysis was employed to verify transcription levels of defense-related genes in tomato leaves treated with IbACP for durations ranging from 0 h (control) to 24 h.
IbACP induced jasmonic acid-related genes (LoxD and AOS) at 2 h, with a significant up-regulation of salicylic acid-dependent gene NPR1 at 24 h. This suggested a temporal antagonistic effect between jasmonic acid and salicylic acid during the early hours of IbACP treatment. Downstream ethylene-responsive regulator genes (ACO1, ETR4, and ERF1) were consistently down-regulated by IbACP at all times. Additionally, IbACP significantly up-regulated the gene expressions of suberization-associated anionic peroxidases (TMP1 and TAP2) at all time points, indicating enhanced suberization of the plant cell wall to prevent pathogen invasion.
IbACP enhances the synthesis of defense hormones and up-regulates downstream defense genes, improving the plant's resistance to biotic stresses.
本研究旨在探讨 IbACP(抗癌肽)对番茄叶片防御相关基因表达的影响,重点关注其在植物防御机制中的作用。
先前,IbACP 从甘薯叶片中分离得到,被鉴定为一种能够诱导番茄悬浮培养液碱化反应的肽。此外,IbACP 被发现可调节人胰腺腺癌细胞的增殖。
使用下一代测序分析阐明 IbACP 对番茄叶片防御相关基因表达的分子影响。
为了评估 IbACP 对防御相关基因表达的影响,分析了转录组数据,涵盖了光合作用、代谢过程和植物防御等多种功能类别。采用半定量逆转录聚合酶链反应分析,验证了 IbACP 处理番茄叶片不同时间(0 h(对照)至 24 h)后防御相关基因的转录水平。
IbACP 在 2 h 诱导茉莉酸相关基因(LoxD 和 AOS),24 h 时水杨酸依赖基因 NPR1 的转录水平显著上调。这表明 IbACP 处理早期,茉莉酸和水杨酸之间存在时间拮抗作用。下游乙烯响应调节因子基因(ACO1、ETR4 和 ERF1)在所有时间点均持续被 IbACP 下调。此外,IbACP 还显著上调了与木质素化相关的阴离子过氧化物酶(TMP1 和 TAP2)的基因表达,表明植物细胞壁的木质素化增强,以防止病原体入侵。
IbACP 增强了防御激素的合成,并上调了下游防御基因,提高了植物对生物胁迫的抗性。