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野生角瓜根结线虫抗性相关基因CmWRKY20的克隆与表达分析 被引量:2

Cloning and Expression Analysis of CmWRKY20 Relevant to Root-knot Nematode Resistance in Wild Cucumis metuliferus
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摘要 WRKY转录因子参与调控与植物免疫反应相关的转录重编程,对植物抗病性发挥调控作用。为了解析WRKY在野生角瓜对根结线虫(RKN)抗性中的作用,通过RT-PCR并结合RACE技术从角瓜根系中克隆CmWRKY20全长cDNA序列,采用DNAStar和DNAMAN进行氨基酸序列与系统进化分析,通过qRT-PCR进行基因表达分析,利用农杆菌介导的烟草叶片细胞转化法进行编码蛋白的亚细胞定位。结果表明,CmWRKY20转录因子cDNA序列全长1603 bp,5′非翻译区646 bp,3′非翻译区320 bp,ORF长度1017 bp,编码338个氨基酸,GenBank登录号MN365875;CmWRKY20具有1个核定位信号和1个WRKY保守结构域,锌指基序为C2H2,归类于WRKY第Ⅱ组,与黄瓜、甜瓜等作物WRKY的氨基酸序列同源性较高,亲缘关系较近;CmWRKY20表达表现为抗病材料高于感病材料,根、茎高于叶片,CmWRKY20受根结线虫快速诱导,水杨酸(SA)和茉莉酸甲酯(MeJA)对CmWRKY20表达既有协同效应又有拮抗作用,CmWRKY20蛋白被定位于细胞膜上。CmWRKY20可能通过SA/JA信号传导参与对根结线虫防卫反应的调控。 WRKY transcription factors are involved in the regulation of transcriptional reprogramming associated with plant immune responses,and play a regulatory role in plant disease resistance.To identify the role of WRKY transcription factor in resistance of Cucumis metuliferus against root-knot nematode(RKN),full-length cDNA sequence of CmWRKY20 was cloned from the roots of C.metuliferus by RT-PCR combined with RACE tecnology.Two softwares of DNAStar and DNAMAN were used for amino acid sequence and phylogenetic evolutionary analyses.Tissue-specific expression characteristics and induced expression profiles of the gene were determined through qRT-PCR,and Agrobacterium-mediated transformation of tobacco leaf cells was used to investigate subcellular localization of its coding proteins.The results showed that full cDNA sequence of CmWRKY20 was 1603 bp in length,including 5′untranslated part of 646 bp,3′untranslated part of 320 bp,an open reading frame of 1017 bp encoding a protein of 338 amino acids consisting of a conserved WRKY domain with a nuclear localization signal and a zinc finger motif of C2H2,belonging to the WRKY subgroupⅡ.CmWRKY20 was deposited in GenBank with Accession No.MN365875,and the amino acid sequence of CmWRKY20 was highly homologous and closely related to cucumber and melon.CmWRKY20 showed higher relative expression in the resistant than the susceptible response,and higher in roots and stems than in leaves.CmWRKY20 was rapidly induced by root-knot nematode infection,salicylic acid(SA)and methyl jasmonate(MeJA)had synergistic or antagonistic effects on the expression of CmWRKY20.CmWRKY20 protein was localized on the cell membrane.CmWRKY20 may be involved in the regulation of defense response to root-knot nematode through SA/JA signal transduction.
作者 叶德友 姜野 王从丽 YE Deyou;JIANG Ye;WANG Congli(Vegetable Research Institute,Gansu Academy of Agricultural Sciences,Lanzhou 730070,China;Northeast Institute of Geography and Agroecology,Chinese Academy of Sciences,Harbin 150081,China)
出处 《华北农学报》 CSCD 北大核心 2020年第4期161-168,共8页 Acta Agriculturae Boreali-Sinica
基金 国家自然科学基金项目(31560506,31760508) 甘肃省自然科学基金项目(17JR5RA185)。
关键词 角瓜 根结线虫 CmWRKY20 克隆 基因表达 亚细胞定位 Cucumis metuliferus Root-knot nematodes CmWRKY20 Cloning Gene expression Subcellular localization
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