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植物细胞中的非转基因基因组修饰。

Nontransgenic genome modification in plant cells.

机构信息

Danziger Innovations Ltd., Mishmar Hashiva Village, Beit Dagan, Israel.

出版信息

Plant Physiol. 2010 Nov;154(3):1079-87. doi: 10.1104/pp.110.164806. Epub 2010 Sep 27.

Abstract

Zinc finger nucleases (ZFNs) are a powerful tool for genome editing in eukaryotic cells. ZFNs have been used for targeted mutagenesis in model and crop species. In animal and human cells, transient ZFN expression is often achieved by direct gene transfer into the target cells. Stable transformation, however, is the preferred method for gene expression in plant species, and ZFN-expressing transgenic plants have been used for recovery of mutants that are likely to be classified as transgenic due to the use of direct gene-transfer methods into the target cells. Here we present an alternative, nontransgenic approach for ZFN delivery and production of mutant plants using a novel Tobacco rattle virus (TRV)-based expression system for indirect transient delivery of ZFNs into a variety of tissues and cells of intact plants. TRV systemically infected its hosts and virus ZFN-mediated targeted mutagenesis could be clearly observed in newly developed infected tissues as measured by activation of a mutated reporter transgene in tobacco (Nicotiana tabacum) and petunia (Petunia hybrida) plants. The ability of TRV to move to developing buds and regenerating tissues enabled recovery of mutated tobacco and petunia plants. Sequence analysis and transmission of the mutations to the next generation confirmed the stability of the ZFN-induced genetic changes. Because TRV is an RNA virus that can infect a wide range of plant species, it provides a viable alternative to the production of ZFN-mediated mutants while avoiding the use of direct plant-transformation methods.

摘要

锌指核酸酶(ZFNs)是真核细胞基因组编辑的有力工具。ZFNs 已被用于模式生物和作物物种的靶向诱变。在动物和人类细胞中,通过直接将基因转移到靶细胞中,通常可以实现瞬时 ZFN 表达。然而,在植物物种中,稳定转化是基因表达的首选方法,并且已经使用表达 ZFN 的转基因植物来恢复由于使用直接基因转移方法进入靶细胞而可能被归类为转基因的突变体。在这里,我们提出了一种替代的非转基因方法,用于 ZFN 的传递和产生突变体植物,使用一种新型的烟草脆裂病毒(TRV)为基础的表达系统,用于间接瞬时递送至完整植物的各种组织和细胞中的 ZFN。TRV 系统感染其宿主,并且可以通过在烟草(Nicotiana tabacum)和矮牵牛(Petunia hybrida)植物中激活突变报告转基因来清楚地观察到病毒 ZFN 介导的靶向突变。TRV 向发育中的芽和再生组织移动的能力使突变体烟草和矮牵牛植物得以恢复。序列分析和突变的传递到下一代证实了 ZFN 诱导的遗传变化的稳定性。由于 TRV 是一种可以感染广泛植物物种的 RNA 病毒,因此它为生产 ZFN 介导的突变体提供了一种可行的替代方法,同时避免了直接植物转化方法的使用。

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