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Polycistronic RNA polymerase II expression vectors for RNA interference based on BIC/miR-155

机译:基于BIC / miR-155的RNA干扰多顺反子RNA聚合酶II表达载体

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摘要

Vector-based RNA interference (RNAi) has emerged as a valuable tool for analysis of gene function. We have developed new RNA polymerase II expression vectors for RNAi, designated SIBR vectors, based upon the non-coding RNA BIC. BIC contains the miR-155 microRNA (miRNA) precursor, and we find that expression of a short region of the third exon of mouse BIC is sufficient to produce miR-155 in mammalian cells. The SIBR vectors use a modified miR-155 precursor stem-loop and flanking BIC sequences to express synthetic miRNAs complementary to target RNAs. Like RNA polymerase III driven short hairpin RNA vectors, the SIBR vectors efficiently reduce target mRNA and protein expression. The synthetic miRNAs can be expressed from an intron, allowing coexpression of a marker or other protein with the miRNAs. In addition, intronic expression of a synthetic miRNA from a two intron vector enhances RNAi. A SIBR vector can express two different miRNAs from a single transcript for effective inhibition of two different target mRNAs. Furthermore, at least eight tandem copies of a synthetic miRNA can be expressed in a polycistronic transcript to increase the inhibition of a target RNA. The SIBR vectors are flexible tools for a variety of RNAi applications.
机译:基于载体的RNA干扰(RNAi)已经成为分析基因功能的有价值的工具。我们已经基于非编码RNA BIC为RNAi开发了新的RNA聚合酶II表达载体,称为SIBR载体。 BIC包含miR-155 microRNA(miRNA)前体,我们发现小鼠BIC第三外显子的短区表达足以在哺乳动物细胞中产生miR-155。 SIBR载体使用修饰的miR-155前体茎环和侧翼BIC序列来表达与靶RNA互补的合成miRNA。像RNA聚合酶III驱动的短发夹RNA载体一样,SIBR载体有效地减少了目标mRNA和蛋白质的表达。可以从内含子表达合成的miRNA,从而使标记物或其他蛋白质与miRNA共表达。另外,来自两个内含子载体的合成miRNA的内含子表达增强了RNAi。 SIBR载体可以从单个转录物中表达两种不同的miRNA,以有效抑制两种不同的目标mRNA。此外,合成miRNA的至少八个串联拷贝可以在多顺反子转录物中表达,以增加对靶RNA的抑制。 SIBR载体是用于各种RNAi应用的灵活工具。

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