Dellagi A, Helibronn J, Avrova A O, Montesano M, Palva E T, Stewart H E, Toth I K, Cooke D E, Lyon G D, Birch P R
Unit of Mycology, Bacteriology and Nematology, Scottish Crop Research Institute, Invergowrie, Dundee, UK.
Mol Plant Microbe Interact. 2000 Oct;13(10):1092-101. doi: 10.1094/MPMI.2000.13.10.1092.
A potato gene encoding a putative WRKY protein was isolated from a cDNA library enriched by suppression subtractive hybridization for sequences upregulated 1 h postinoculation 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.
从一个通过抑制性消减杂交富集的cDNA文库中分离出一个编码假定WRKY蛋白的马铃薯基因,该文库针对接种胡萝卜软腐欧文氏菌亚种黑胫亚种1小时后上调的序列。该cDNA编码一个由172个氨基酸组成的假定多肽,包含一个带有锌指基序的单一WRKY结构域,前面有一个潜在的核定位位点。在与致病疫霉的亲和互作中,St-WRKY1强烈上调,但在非亲和互作中仅微弱上调,在所有情况下,它都与I类内切几丁质酶共同调控,将其表达与已知的防御反应联系起来。虽然St-WRKY1被胡萝卜软腐欧文氏菌培养滤液(CF)强烈诱导,证实它是一个激发子诱导基因,但在用水杨酸、茉莉酸甲酯、乙烯或创伤处理后未检测到这种诱导。用含有表达胡萝卜软腐欧文氏菌果胶酸裂解酶基因pelB和pelD的质粒的重组大肠杆菌的CF处理马铃薯叶片后,St-WRKY1上调,这表明这些基因编码的蛋白质或其活性产生的寡半乳糖醛酸引发了与St-WRKY1相关的马铃薯防御途径。