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基于无病症类病毒的环状 RNA 载体靶向植物基因沉默。

A circular RNA vector for targeted plant gene silencing based on an asymptomatic viroid.

机构信息

Institute for Integrative Systems Biology (I2SysBio), Consejo Superior de Investigaciones Científicas (CSIC) - Universitat de València (UV), Parc Científic, Cat. Agustín Escardino 9, 46980, Paterna, Spain.

Instituto de Biología Molecular y Celular de Plantas (IBMCP), Consejo Superior de Investigaciones Científicas (CSIC) - Universitat Politècnica de València, CPI 8E, Av. de los Naranjos s/n, 46022, Valencia, Spain.

出版信息

Plant J. 2022 Oct;112(1):284-293. doi: 10.1111/tpj.15929. Epub 2022 Aug 19.

DOI:10.1111/tpj.15929
PMID:35916236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9804161/
Abstract

Gene silencing for functional studies in plants has been largely facilitated by manipulating viral genomes with inserts from host genes to trigger virus-induced gene silencing (VIGS) against the corresponding mRNAs. However, viral genomes encode multiple proteins and can disrupt plant homeostasis by interfering with endogenous cell mechanisms. To try to circumvent this functional limitation, we have developed a silencing method based on the minimal autonomously-infectious nucleic acids currently known: viroids, which lack proven coding capability. The genome of Eggplant latent viroid, an asymptomatic viroid, was manipulated with insertions ranging between 21 and 42 nucleotides. Our results show that, although larger insertions might be tolerated, the maintenance of the secondary structure appears to be critical for viroid genome stability. Remarkably, these modified ELVd molecules are able to induce systemic infection promoting the silencing of target genes in eggplant. Inspired by the design of artificial microRNAs, we have developed a simple and standardized procedure to generate stable insertions into the ELVd genome capable of silencing a specific target gene. Analogously to VIGS, we have termed our approach viroid-induced gene silencing, and demonstrate that it is a promising tool for dissecting gene functions in eggplant.

摘要

基因沉默在植物功能研究中得到了广泛应用,方法是通过操纵带有宿主基因插入物的病毒基因组来触发针对相应 mRNA 的病毒诱导基因沉默(VIGS)。然而,病毒基因组编码多种蛋白质,通过干扰内源性细胞机制来破坏植物的内稳态。为了尝试规避这种功能限制,我们开发了一种基于最小自主感染性核酸的沉默方法:类病毒,它缺乏已证实的编码能力。茄科隐潜病毒的基因组经过操纵,插入物长度在 21 到 42 个核苷酸之间。我们的结果表明,尽管较大的插入物可能被容忍,但二级结构的维持对于类病毒基因组的稳定性似乎至关重要。值得注意的是,这些经过修饰的 ELVd 分子能够诱导系统感染,促进茄子中靶基因的沉默。受人工 microRNA 设计的启发,我们开发了一种简单且标准化的程序,可将稳定的插入物插入 ELVd 基因组中,从而沉默特定的靶基因。类似于 VIGS,我们将我们的方法称为类病毒诱导的基因沉默,并证明它是解析茄子中基因功能的一种很有前途的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/66edea43d5df/TPJ-112-284-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/db8798e6742b/TPJ-112-284-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/5c5ab152870f/TPJ-112-284-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/3c0ba4c216f7/TPJ-112-284-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/66edea43d5df/TPJ-112-284-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/db8798e6742b/TPJ-112-284-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/5c5ab152870f/TPJ-112-284-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/3c0ba4c216f7/TPJ-112-284-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7de/9804161/66edea43d5df/TPJ-112-284-g002.jpg

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