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番茄SlJAZ7的抗病功能及与SlTGA7的互作OA北大核心CSTPCD

Disease resistance of SlJAZ7 and its interaction with SlTGA7 in tomato

中文摘要英文摘要

[目的]细菌性斑点病是导致番茄 Solanum lycopersicum 减产的主要因素之一,丁香假单胞菌(Pseudomonas syringae pv.tomato DC3000,Pst DC3000)是细菌性斑点病的致病因子之一.瞬时沉默番茄JAZ7 基因导致其对Pst DC3000 的敏感性增加,然而,验证JAZ7 基因抗细菌性斑点病的直接证据及其作用机理的报道较少.本研究从番茄叶片中克隆得到SlJAZ7 基因,创制稳定遗传的过表达SlJAZ7 的转基因番茄,分析其抗病功能和机理,研究其在转录水平和蛋白水平上与抗病性密切相关的SlTGA7 的关系,为有效防治细菌性斑点病提供理论基础.[方法]通过野生型和转基因番茄接种Pst DC3000 的表型差异分析,鉴定SlJAZ7 基因的抗病功能.使用RT-qPCR分析SlJAZ7 和SlTGA7 基因在Pst DC3000、茉莉酸甲酯(Methyl jasmonate,MeJA)和水杨酸(Salicylic acid,SA)处理下的表达模式和组织特异性.利用烟草瞬时表达的方法研究SIJAZ7 和SlTGA7 蛋白的亚细胞定位.利用酵母双杂交(Y2H)试验、双分子荧光互补(BiFC)试验和蛋白下拉(pull down)试验研究SlJAZ7 蛋白与SlTGA7 蛋白的互作关系,验证SlJAZ7 的抗病功能和可能的抗病机理.[结果]过表达SlJAZ7 基因的转基因番茄叶片在Pst DC3000 处理时受到的过氧化损伤较野生型更少,转基因株系中SlTGA7 表达量升高,SlJAZ7 基因在营养器官中高表达,且受到Pst DC3000 诱导,响应MeJA、SA处理,SlTGA7 基因在同样的处理下呈相反的变化趋势.SlJAZ7 和SlTGA7 蛋白均定位于细胞核.Y2H、BiFC和pull down试验同时证明SlJAZ7 蛋白和SlTGA7 蛋白存在互作关系.[结论]过表达SlJAZ7 基因有利于减少活性氧积累,提高番茄抗病性,同时SlJAZ7 在转录水平正调控SlTGA7 基因表达.SlJAZ7 与SlTGA7 存在互作,推测SIJAZ7 基因可能通过提高Pst DC3000 病原菌侵染时SITGA7 基因的表达量,启动SITGA7 下游抗病基因的表达来提高转基因番茄的抗病性,也可能通过与SITGA7 蛋白结合,影响其调控MYC等转录因子的活性.这为进一步研究SlJAZ7 的作用机制奠定了基础.

[Objective]Bacterial spot disease is one of the main factors leading to tomato(Solanum lycopersicum)yield reduction,and Pseudomonas syringae pv.tomato DC3000(Pst DC3000)is one of the pathogenic factors of bacterial spot disease.Transient silencing of JAZ7 gene in tomato results in its increased susceptibility to Pst DC3000.At present,there are a few reports to verify the resistance function and mechanism of JAZ7 gene in tomato.In this study,we cloned SlJAZ7 gene in tomato leaves,and a stable genetic transgenic tomato with overexpression of SlJAZ7 was created to analyze its resistance function and mechanism,and the relationship between SlJAZ7 and SlTGA7,which is closely related to disease resistance,was studied at the transcriptional and protein levels,providing a theoretical basis for effective prevention and control of bacterial spot disease.[Method]The resistance function of SlJAZ7 gene was determined by the phenotypic difference between wild type and transgenic tomato inoculated with Pst DC3000.RT-qPCR was used to analyze the tissue-specific expression of SlJAZ7 gene and SlTGA7 gene under Pst DC3000,methyl jasmonate(MeJA)and salicylic acid(SA)treatments.The subcellular localization of SIJAZ7 and SlTGA7 proteins was studied by transient expression of tobacco.The interaction between SlJAZ7 and SlTGA7 was verified by Y2H,BiFC and pull down experiments,to verify the disease resistance function and possible mechanism of SlJAZ7.[Result]Transgenic tomato leaves overexpressing SlJAZ7 gene had lower peroxidation damage than wild type when treated with pathogens,the expression level of SlTGA7 in transgenic lines increased.SlJAZ7 gene was highly expressed in nutrient tissues.SlJAZ7 gene was induced by Pst DC3000 and in response to MeJA and SA treatments.SlTGA7 gene showed opposite change trend under the same treatment.Both SlJAZ7 and SlTGA7 proteins were located in the nucleus.All Y2H,BiFC and pull down experiments proved the interaction between SlJAZ7 and SlTGA7.[Conclusion]Overexpression of SlJAZ7 gene can reduce the accumulation of reactive oxygen species and improve tomato disease resistance.SlJAZ7 positively regulates SlTGA7 gene expression at the transcriptional level.SlJAZ7 interacts with SlTGA7.It is speculated that SIJAZ7 gene may improve the disease resistance of transgenic tomato by increasing the expression level of SITGA7 gene during pathogen infection,initiating the expression of downstream resistance genes of SITGA7,or by binding with SITGA7 protein,affecting its regulation of MYC and other transcription factors.The result lays a foundation for further research on the mechanism of SlJAZ7.

林晨俞;郭鑫;王文娟;翟敏;曹颖杰;王梦月;赵平娟;于晓惠

海南大学热带农林学院,海南海口 570228||中国热带农业科学院热带生物技术研究所/热带作物生物育种国家重点实验室,海南海口 571101海南大学热带农林学院,海南海口 570228中国热带农业科学院热带生物技术研究所/热带作物生物育种国家重点实验室,海南海口 571101

园艺学与植物营养学

番茄SlJAZ7蛋白互作抗病性茉莉酸甲酯水杨酸

TomatoSlJAZ7Protein interactionDisease resistanceMethyl jasmonateSalicylic acid

《华南农业大学学报》 2024 (004)

525-534 / 10

国家自然科学基金(31960526);海南省研究生创新课题(Qhys2022-78)

10.7671/j.issn.1001-411X.202312017

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