Lamberton Janelle S, Christian Allen T
Biology and Biotechnology Research Program, Lawrence Livermore National Laboratory, PO Box 808, L-448, Livermore, CA, 94551, USA.
Mol Biotechnol. 2003 Jun;24(2):111-20. doi: 10.1385/MB:24:2:111.
The utility of short interfering RNA (siRNA) as a means of gene silencing depends on several factors. These include the degree to which a gene can be silenced, the length of time for which the gene remains silenced, the degree of recovery of gene function, and the effects of the silencing process on general cell functions. We hypothesized that changing the nucleic acid composition of the siRNA constructs used for silencing would affect these parameters. With siRNA gene silencing of the glucose-6-phosphate dehydrogenase gene as a baseline, we found that siDNA molecules have an effect that is similar in duration but lesser in degree, whereas hybrid DNA:RNA molecules have an effect that is enormously greater in both duration and degree.
短干扰RNA(siRNA)作为一种基因沉默手段的效用取决于几个因素。这些因素包括基因能够被沉默的程度、基因保持沉默的时间长度、基因功能恢复的程度以及沉默过程对一般细胞功能的影响。我们假设,改变用于沉默的siRNA构建体的核酸组成会影响这些参数。以葡萄糖-6-磷酸脱氢酶基因的siRNA基因沉默作为基线,我们发现siDNA分子具有持续时间相似但程度较小的效果,而杂交DNA:RNA分子在持续时间和程度上都具有极大更强的效果。