Stein Paula, Svoboda Petr, Schultz Richard M
Department of Biology, University of Pennsylvania, Philadelphia, PA, USA,
Methods Mol Biol. 2013;957:135-51. doi: 10.1007/978-1-62703-191-2_9.
RNA interference (RNAi) is an evolutionary conserved gene-silencing pathway that can be efficiently utilized as a tool to study gene function. RNAi is initiated by long double-stranded RNAs (dsRNAs), which are processed into small duplexes called small-interfering RNAs (siRNAs). In turn, these duplexes target mRNAs for degradation in a sequence-specific manner. Mouse oocytes, unlike most mammalian cell types, lack an interferon response to long dsRNA. Moreover, they are a rare example of a mammalian cell type with a robust endogenous RNAi pathway. For these reasons microinjection of either long dsRNAs or siRNAs results in efficient, sequence-specific gene silencing. Here, we describe a protocol for preparation and microinjection of long dsRNA into mouse oocytes.
RNA干扰(RNAi)是一种进化保守的基因沉默途径,可有效用作研究基因功能的工具。RNAi由长双链RNA(dsRNA)引发,dsRNA被加工成称为小干扰RNA(siRNA)的小双链体。反过来,这些双链体以序列特异性方式靶向mRNA进行降解。与大多数哺乳动物细胞类型不同,小鼠卵母细胞对长dsRNA缺乏干扰素反应。此外,它们是具有强大内源性RNAi途径的哺乳动物细胞类型的罕见例子。由于这些原因,显微注射长dsRNA或siRNA都会导致高效的、序列特异性的基因沉默。在这里,我们描述了一种将长dsRNA制备并显微注射到小鼠卵母细胞中的方案。