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利用 RNA 干扰构建体进行 agroinfiltration 瞬时沉默葡萄基因 VvPGIP1。

Transient silencing of the grapevine gene VvPGIP1 by agroinfiltration with a construct for RNA interference.

机构信息

CRA-VIT Centro di ricerca per la viticoltura, Conegliano, TV, Italy.

出版信息

Plant Cell Rep. 2012 Jan;31(1):133-43. doi: 10.1007/s00299-011-1147-2. Epub 2011 Sep 20.

Abstract

Grapevine is an economically important crop, and the recent completion of its genome makes it possible to study the function of specific genes through reverse genetics. However, the analysis of gene function by RNA interference (RNAi) in grapevine is difficult, because the generation of stable transgenic plants has low efficiency and is time consuming. Recently, transient expression of genes in grapevine leaves has been obtained by Agrobacterium tumefaciens infiltration (agroinfiltration). We therefore tested the possibility to silence grapevine genes by agroinfiltration of RNAi constructs. A construct to express a double strand RNA (dsRNA) corresponding to the defense-related gene VvPGIP1, encoding a polygalacturonase-inhibiting protein (PGIP), was obtained and transiently expressed by agroinfiltration in leaves of grapevine plants grown in vitro. Expression of VvPGIP1 and accumulation of PGIP activity were strongly induced by infiltration with control bacteria, but not with bacteria carrying the dsRNA construct, indicating that the gene was efficiently silenced. In contrast, expression of another defense-related gene, VST1, encoding a stilbene synthase, was unaffected by the dsRNA construct. We have therefore demonstrated the possibility of transient down-regulation of grapevine genes by agroinfiltration of constructs for the expression of dsRNA. This system can be employed to evaluate the effectiveness of constructs that can be subsequently used to generate stable RNAi transgenic plants.

摘要

葡萄是一种经济上重要的作物,其基因组最近的完成使得通过反向遗传学研究特定基因的功能成为可能。然而,通过 RNA 干扰(RNAi)在葡萄中分析基因功能具有一定难度,因为稳定转化植物的产生效率低且耗时。最近,通过根癌农杆菌浸润(agroinfiltration)实现了葡萄叶片中基因的瞬时表达。因此,我们测试了通过 agroinfiltration RNAi 构建物沉默葡萄基因的可能性。获得了一个表达与防御相关基因 VvPGIP1 双链 RNA(dsRNA)的构建体,该基因编码多聚半乳糖醛酸酶抑制蛋白(PGIP),并通过在体外生长的葡萄植物叶片中的 agroinfiltration 瞬时表达。VvPGIP1 的表达和 PGIP 活性的积累被对照细菌浸润强烈诱导,但携带 dsRNA 构建体的细菌浸润则没有,表明该基因被有效沉默。相比之下,另一个防御相关基因 VST1,编码芪合酶,不受 dsRNA 构建体的影响。因此,我们已经证明了通过 agroinfiltration 表达 dsRNA 的构建体瞬时下调葡萄基因的可能性。该系统可用于评估随后用于生成稳定 RNAi 转基因植物的构建体的有效性。

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