Le Lien Quynh, Lorenz Yvonne, Scheurer Stephan, Fötisch Kay, Enrique Ernesto, Bartra Joan, Biemelt Sophia, Vieths Stefan, Sonnewald Uwe
Institut für Pflanzengenetik and Kulturpflanzenforschung Gatersleben, Corrensstrasse 3, 06466 Gatersleben, Germany.
Plant Biotechnol J. 2006 Mar;4(2):231-42. doi: 10.1111/j.1467-7652.2005.00175.x.
Plant genetic engineering has the potential to introduce new allergenic proteins into foods but, at the same time, it can be used to remove established allergens. Here, we report the molecular characterization of Lyc e 3, a new tomato (Lycopersicon esculentum) allergen, and the efficient down-regulation of its expression in transgenic tomato plants. Following the identification of an immunoglobulin E (IgE)-binding 9-kDa polypeptide in tomato peel, designated Lyc e 3, its partial amino acid sequence was determined by N-terminal protein sequencing. Sequence comparison revealed that Lyc e 3 encodes a nonspecific lipid transfer protein (ns-LTP). In plants, ns-LTPs are encoded by large gene families which differ in primary amino acid sequence, expression and proposed cellular function. To identify Lyc e 3 encoding complementary DNAs (cDNAs), public tomato expressed sequence tag (EST) databases were screened for ns-LTP sequences. Following this strategy, two cDNAs, LTPG1 and LTPG2, with high homology to the N-terminal sequence of Lyc e 3, were identified. Ectopic expression of LTPG1 and LTPG2 in Escherichia coli, followed by immunoblotting, verified their IgE reactivity. Subsequently, transgenic tomato plants constitutively expressing LTPG1- or LTPG2-specific double-stranded RNA interference (dsRNAi) constructs were created and tested for the suppression of Lyc e 3 accumulation. Efficient silencing of Lyc e 3 was documented by Northern and Western blotting. In both cases, Lyc e 3 accumulation was decreased to levels below the detection limit (less than 0.5% of the wild-type protein). The allergenic potential of Lyc e 3-deficient tomato fruits was tested by measuring histamine release from sensitized human basophils stimulated with transgenic and parental lines. These assays revealed a strong (10- to 100-fold) decrease in histamine release of human basophils challenged with transgenic fruit extracts when compared with control extracts. These results demonstrate the feasibility of creating low allergenic tomato fruits by means of dsRNAi inhibition.
植物基因工程有可能将新的致敏蛋白引入食品,但与此同时,它也可用于去除已有的过敏原。在此,我们报告了一种新的番茄(Lycopersicon esculentum)过敏原Lyc e 3的分子特征,以及在转基因番茄植株中其表达的有效下调。在鉴定出番茄果皮中一种与免疫球蛋白E(IgE)结合的9 kDa多肽(命名为Lyc e 3)后,通过N端蛋白质测序确定了其部分氨基酸序列。序列比较显示,Lyc e 3编码一种非特异性脂质转移蛋白(ns-LTP)。在植物中,ns-LTP由庞大的基因家族编码,这些家族在一级氨基酸序列、表达及推测的细胞功能方面存在差异。为了鉴定编码Lyc e 3的互补DNA(cDNA),在公共番茄表达序列标签(EST)数据库中筛选ns-LTP序列。按照此策略,鉴定出了两个与Lyc e 3的N端序列具有高度同源性的cDNA,即LTPG1和LTPG2。LTPG1和LTPG2在大肠杆菌中的异位表达,随后进行免疫印迹,证实了它们与IgE的反应性。随后,构建了组成型表达LTPG1或LTPG2特异性双链RNA干扰(dsRNAi)构建体的转基因番茄植株,并检测其对Lyc e 3积累的抑制作用。Northern印迹和Western印迹证明了Lyc e 3的有效沉默。在这两种情况下,Lyc e 3的积累均降至检测限以下(低于野生型蛋白的0.5%)。通过测量用转基因品系和亲本品系刺激的致敏人嗜碱性粒细胞释放组胺,测试了缺乏Lyc e 3的番茄果实的致敏潜力。这些试验表明,与对照提取物相比,用转基因果实提取物刺激的人嗜碱性粒细胞释放组胺的量大幅减少(10至100倍)。这些结果证明了通过dsRNAi抑制来培育低致敏性番茄果实的可行性。