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利用碳纳米载体在烟草植株中实现高效瞬时基因敲低

Efficient Transient Gene Knock-down in Tobacco Plants Using Carbon Nanocarriers.

作者信息

Demirer Gozde S, Landry Markita P

机构信息

Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720, USA.

California Institute for Quantitative Biosciences, QB3, University of California, Berkeley, CA 94720, USA.

出版信息

Bio Protoc. 2021 Jan 5;11(1):e3897. doi: 10.21769/BioProtoc.3897.

Abstract

Gene knock-down in plants is a useful approach to study genotype-phenotype relationships, render disease resistance to crops, and enable efficient biosynthesis of molecules in plants. Small interfering RNA (siRNA)-mediated gene silencing is one of the most common ways to achieve gene knock-down in plants. Traditionally, siRNA is delivered into intact plant cells by coding the siRNA sequences into DNA vectors, which are then delivered through viral and/or bacterial methods. In this protocol, we provide an alternative direct delivery method of siRNA molecules into intact plant cells for efficient transient gene knock-down in model tobacco plant, , leaves. Our approach uses one dimensional carbon-based nanomaterials, single-walled carbon nanotubes (SWNTs), to deliver siRNA, and does not rely on viral/bacterial delivery. The distinct advantages of our method are i) there is no need for DNA coding of siRNA sequences, ii) this abiotic method could work in a broader range of plant species than biotic methods, and iii) there are fewer regulatory complications when using abiotic delivery methods, whereby gene silencing is transient without permanent modification of the plant genome. .

摘要

植物中的基因敲低是研究基因型与表型关系、赋予作物抗病性以及实现植物中分子高效生物合成的一种有用方法。小干扰RNA(siRNA)介导的基因沉默是在植物中实现基因敲低的最常见方法之一。传统上,通过将siRNA序列编码到DNA载体中,然后通过病毒和/或细菌方法将其导入完整的植物细胞中。在本方案中,我们提供了一种将siRNA分子直接导入完整植物细胞的替代方法,用于在模式烟草植物叶片中高效瞬时基因敲低。我们的方法使用一维碳基纳米材料单壁碳纳米管(SWNTs)来递送siRNA,并且不依赖于病毒/细菌递送。我们方法的显著优点是:i)无需对siRNA序列进行DNA编码;ii)这种非生物方法比生物方法能在更广泛的植物物种中起作用;iii)使用非生物递送方法时监管复杂性更少,基因沉默是瞬时的,不会对植物基因组进行永久修饰。

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