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首页> 外文期刊>Scientia horticulturae >Transient expression of siRNA targeted against the TYLCV AV1, AC1 and AC3 genes for high resistance in tomato
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Transient expression of siRNA targeted against the TYLCV AV1, AC1 and AC3 genes for high resistance in tomato

机译:靶向TYLCV AV1,AC1和AC3基因的siRNA的瞬时表达可实现番茄的高抗性

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摘要

Tomato yellow leaf curl virus (TYLCV) is a globally devastating disease that affects the production of many crops, particularly tomato, leading to considerable economic losses. RNA interference, which allows sequence-specific gene silencing at the post-transcriptional level, is an effective method to obtain virus-resistant lines of crops. Agrobacterium-mediated transient expression assay has emerged as a rapid and useful approach to evaluate gene functions in plants without the need to produce transgenic lines. In this study, we transformed the plant expression vector pBIN438-AV1-AC1-AC3(i/r), which consists of the inverted repeat of Delta AV1, Delta AC1, and Delta AC3 fusion fragments into Agrobacterium tumefaciens EHA105 to generate tomato lines with high viral resistance. The viral resistance of the fusion gene was evaluated by transient expression. The test plants did not show disease symptoms at 35 d postinoculation with TYLCV. This study provided an important method for plant antiviral breeding and safe tomato production. (C) 2014 Elsevier B.V. All rights reserved.
机译:番茄黄叶卷曲病毒(TYLCV)是一种具有全球破坏性的疾病,影响许多农作物(尤其是番茄)的生产,从而造成可观的经济损失。 RNA干扰使转录后水平的序列特异性基因沉默,是获得农作物抗病毒品系的有效方法。农杆菌介导的瞬时表达测定法已经成为评估植物中基因功能而无需产生转基因品系的一种快速而有用的方法。在这项研究中,我们将植物表达载体pBIN438-AV1-AC1-AC3(i / r)转化为根癌农杆菌EHA105,以将其与ΔΔV1,ΔΔAC1和ΔΔAC3融合片段的反向重复序列结合起来,以产生高病毒抵抗力。通过瞬时表达评估融合基因的病毒抗性。 TYLCV接种后35 d,受试植物未显示疾病症状。该研究为植物抗病毒育种和安全番茄生产提供了重要手段。 (C)2014 Elsevier B.V.保留所有权利。

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