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首页> 外文期刊>Molecular Plant-Microbe Interactions >A Potato Gene Encoding a WRKY-like Transcription Factor Is Induced in Interactions with Erwinia carotovora subsp. atroseptica and Phytophthora infestans and Is Coregulated with Class I Endochitinase Expression
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A Potato Gene Encoding a WRKY-like Transcription Factor Is Induced in Interactions with Erwinia carotovora subsp. atroseptica and Phytophthora infestans and Is Coregulated with Class I Endochitinase Expression

机译:马铃薯基因编码WRKY样转录因子诱导与胡萝卜欧文亚种的相互作用。 atroseptica和疫霉菌感染,并与I类内切酶表达共调节

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A potato gene encoding a putative WRKY protein was isolated from a cDNA library enriched by suppression subtractive hybridization for sequences upregulated 1 h post-inoculation with Erwinia carotovora subsp. atroseptica . The cDNA encodes a putative polypeptide of 172 amino acids, containing a single WRKY domain with a zinc finger motif and preceded by a potential nuclear localization site. St-WRKY1 was strongly upregulated in compatible, but only weakly in incompatible, interactions with Phytophthora infestans where, in all cases, it was coregulated with class I endochitinase, associating its expression with a known defense response. Whereas St-WRKY1 was strongly induced by E. carotovora culture filtrate (CF), confirming it to be an elicitor-induced gene, no such induction was detected after treatment with salicylic acid, methyl jasmonate, ethylene, or wounding. St-WRKY1 was upregulated by treatment of potato leaves with CFs from recombinant Escherichia coli containing plasmids expressing E. carotovora pectate lyase genes pelB and pelD , suggesting that either proteins encoded by these genes, or oligogalacturonides generated by their activity, elicit a potato defense pathway associated with St-WRKY1 .
机译:从通过抑制消减杂交富集的cDNA文库中分离出编码推定的WRKY蛋白的马铃薯基因,用于接种胡萝卜欧文氏菌亚种1小时后上调的序列。 atroseptica。 cDNA编码一个172个氨基酸的推定多肽,该多肽包含一个带有锌指基序的WRKY结构域,并在其之前具有潜在的核定位位点。 St-WRKY1在与疫霉疫菌的相容性相互作用中被强烈上调,但在不相容性中被弱表达,在所有情况下,St-WRKY1都与I类内切壳多糖酶共调节,从而使其表达与已知的防御反应相关。尽管St-WRKY1是由胡萝卜肠杆菌培养物滤液(CF)强烈诱导的,确认它是引发剂诱导的基因,但在用水杨酸,茉莉酸甲酯,乙烯或伤口处理后未检测到这种诱导。 St-WRKY1通过用重组大肠杆菌的CF处理马铃薯叶而被上调,重组大肠杆菌含有表达胡萝卜果胶果胶酸裂解酶基因pelB和pelD的质粒,表明这些基因编码的蛋白质或由其活性产生的寡半乳糖苷均可引发马铃薯防御途径。与St-WRKY1相关联。

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