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首页> 外文期刊>Plant physiology >New Generation of Artificial MicroRNA and Synthetic Trans-Acting Small Interfering RNA Vectors for Efficient Gene Silencing in Arabidopsis~(1[W][OPEN])
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New Generation of Artificial MicroRNA and Synthetic Trans-Acting Small Interfering RNA Vectors for Efficient Gene Silencing in Arabidopsis~(1[W][OPEN])

机译:拟南芥〜(1 [W] [OPEN])中有效基因沉默的新一代人工MicroRNA和合成反式小干扰RNA载体

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Artificial microRNAs (amiRNAs) and synthetic trans-acting small interfering RNAs (syn-tasiRNAs) are used for small RNA-based, specific gene silencing or knockdown in plants. Current methods to generate amiRNA or syn-tasiRNA constructs are not well adapted for cost-effective, large-scale production or for multiplexing to specifically suppress multiple targets. Here, we describe simple, fast, and cost-effective methods with high-throughput capability to generate amiRNA and multiplexed syn-tasiRNA constructs for efficient gene silencing in Arabidopsis (Arabidopsis thaliana) and other plant species. amiRNA or syn-tasiRNA inserts resulting from the annealing of two overlapping and partially complementary oligonucleotides are ligated directionally into a zero background Bsal/ccdB-based expression vector. BsaI/ccdB vectors for amiRNA or syn-tasiRNA cloning and expression contain a modified version of Arabidopsis MIR390a or TAS1c precursors, respectively, in which a fragment of the endogenous sequence was substituted by a ccdB cassette flanked by two BsaI sites. Several amiRNA and syn-tasiRNA sequences designed to target one or more endogenous genes were validated in transgenic plants that (1) exhibited the expected phenotypes predicted by loss of target gene function, (2) accumulated high levels of accurately processed amiRNAs or syn-tasiRNAs, and (3) had reduced levels of the corresponding target RNAs.
机译:人工microRNA(amiRNA)和合成反式小干扰RNA(syn-tasiRNA)用于植物中基于小RNA的特异性基因沉默或敲低。当前产生amiRNA或syn-tasiRNA构建体的方法不适用于成本有效的大规模生产或用于特异性抑制多个靶标的多路复用。在这里,我们描述了具有高通量能力的简单,快速且具有成本效益的方法,可生成amiRNA和合成的syn-tasiRNA构建体,以在拟南芥(Arabidopsis thaliana)和其他植物物种中实现有效的基因沉默。将两个重叠且部分互补的寡核苷酸退火产生的amiRNA或syn-tasiRNA插入片段定向连接到基于零背景Bsal / ccdB的表达载体中。用于amiRNA或syn-tasiRNA克隆和表达的BsaI / ccdB载体分别包含拟南芥MIR390a或TAS1c前体的改良版,其中内源序列的片段被两侧是两个BsaI位点的ccdB盒替代。在转基因植物中验证了设计用于靶向一种或多种内源基因的几种amiRNA和syn-tasiRNA序列,这些基因(1)表现出靶基因功能丧失所预测的预期表型,(2)积累了高水平的经过精确加工的amiRNA或syn-tasiRNA (3)的水平降低了相应的靶RNA。

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