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A Simple Retroelement Based Knock-Down System in Dictyostelium: Further Insights into RNA Interference Mechanisms

机译:一个简单的基于还原铁基的介导基因敲除系统:RNA干扰机制的进一步见解。

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摘要

Characteristics of DIRS-1 Mediated Knock-DownsWe have previously shown that the most abundant Dictyostelium discoideum retroelement DIRS-1 is suppressed by RNAi mechanisms. Here we provide evidence that both inverted terminal repeats have strong promoter activity and that bidirectional expression apparently generates a substrate for Dicer. A cassette containing the inverted terminal repeats and a fragment of a gene of interest was sufficient to activate the RNAi response, resulting in the generation of ~21 nt siRNAs, a reduction of mRNA and protein expression of the respective endogene. Surprisingly, no transitivity was observed on the endogene. This was in contrast to previous observations, where endogenous siRNAs caused spreading on an artificial transgene. Knock-down was successful on seven target genes that we examined. In three cases a phenotypic analysis proved the efficiency of the approach. One of the target genes was apparently essential because no knock-out could be obtained; the RNAi mediated knock-down, however, resulted in a very slow growing culture indicating a still viable reduction of gene expression.
机译:DIRS-1介导的敲低的特征我们之前已经表明,RNAi机制可抑制最丰富的盘基网柄菌逆向繁殖元件DIRS-1。在这里,我们提供的证据表明,两个反向末端重复序列均具有强大的启动子活性,并且双向表达显然可产生Dicer的底物。包含反向末端重复序列和目的基因片段的盒足以激活RNAi反应,从而导致〜21 nt siRNA的产生,相应内基因的mRNA和蛋白质表达降低。令人惊讶地,在内生基因上未观察到传递性。这与以前的观察结果相反,在先前的观察中,内源性siRNA导致在人工转基因上扩散。在我们研究的七个靶基因上,敲除成功。在三种情况下,表型分析证明了该方法的有效性。目标基因之一显然是必不可少的,因为无法获得基因敲除。然而,RNAi介导的敲低导致培养物生长非常缓慢,表明基因表达仍然可行。

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