Kerschen Arthur, Napoli Carolyn A, Jorgensen Richard A, Müller Andreas E
Department of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA.
FEBS Lett. 2004 May 21;566(1-3):223-8. doi: 10.1016/j.febslet.2004.04.043.
RNA interference (RNAi) can be used to study gene function by effecting degradation of the targeted transcript. However, the effectiveness of transgene-induced RNAi among multiple target genes has not been compared systematically. To this end, we developed a relative quantitative RT-PCR protocol that allows use of a single internal standard over a wide range of target gene expression levels. Using this method in an analysis of transgenic Arabidopsis thaliana RNAi lines targeting 25 different endogenes revealed that independent, homozygous, single-copy (sc) T4 lines targeting the same gene generally reduce transcript levels to the same extent, whereas multi-copy RNAi lines differed in the degree of target reduction and never exceeded the effect of sc transgenes. The maximal reduction of target transcript levels varied among targets. These observations suggest that each target sequence possesses an inherent degree of susceptibility to dsRNA-mediated degradation.
RNA干扰(RNAi)可通过促使靶向转录本降解来研究基因功能。然而,尚未系统比较过转基因诱导的RNAi在多个靶基因中的有效性。为此,我们开发了一种相对定量RT-PCR方案,该方案允许在广泛的靶基因表达水平上使用单一内标。在对靶向25个不同内源基因的转基因拟南芥RNAi株系进行分析时使用此方法,结果表明,靶向同一基因的独立、纯合、单拷贝(sc)T4株系通常会将转录本水平降低到相同程度,而多拷贝RNAi株系在靶标降低程度上存在差异,且从未超过sc转基因的效果。靶转录本水平的最大降低程度因靶标而异。这些观察结果表明,每个靶序列对dsRNA介导的降解都具有一定程度的固有敏感性。