Graduate School of Science and Technology, Shinshu University, Matsumoto, Nagano 390-8621, Japan.
J Insect Physiol. 2013 Apr;59(4):400-7. doi: 10.1016/j.jinsphys.2013.01.009. Epub 2013 Jan 31.
RNA interference (RNAi) is a powerful and convenient tool not only for functional analysis of specific genes, but also for large-scale screening of gene function in insects; however, reports on its efficiency throughout development in a single species are limited. We demonstrate here that non-cell autonomous RNAi by injection of double-stranded RNA (dsRNA) knocks down targeting genes in most developmental stages in the sawfly, Athalia rosae. Injection of dsRNA targeting the green fluorescence protein (gfp) gene into eggs of a transgenic strain carrying the constitutively expressing gfp gene resulted in the absence of GFP fluorescence during embryogenesis, while a portion of the gfp dsRNA-injected embryos began exhibiting GFP fluorescence at late embryogenesis. When gfp dsRNA was injected into parental female pupae, the RNAi effect was carried over to all embryos of the next generation and the effect lasted until mid-larval stages. Parental injection of dsRNA was more efficient than embryonic injection in terms of penetrance of the effect and the survival rate. After injection of gfp dsRNA into last instar larvae, the RNAi effect was sustained during prepupal and pupal stages and in adults. The gfp gene transcript markedly decreased in these knockdown phenotypes. It was revealed by employing fluorescence-labeled dsRNA that injected dsRNA was taken up in internal organs. Knockdown of an endogenous gene, Distal-less (Dll), resulted in typical phenotypes represented by the lack and malformation of Dll-expressing organs, such as distal parts of the appendages and wing edges without showing off-target effects. In contrast, RNAi by dsRNA injection seems to be hardly effective in mid- to late-larval stages.
RNA 干扰(RNAi)不仅是一种强大而方便的工具,可用于特定基因的功能分析,还可用于大规模筛选昆虫中的基因功能;然而,在单一物种中,有关其在整个发育过程中效率的报道是有限的。我们在这里证明,通过注射双链 RNA(dsRNA)进行非细胞自主 RNAi 可以在鳞翅目锯蝇中大多数发育阶段敲低靶向基因。将靶向绿色荧光蛋白(gfp)基因的 dsRNA 注射到携带组成型表达 gfp 基因的转基因品系的卵中,导致 GFP 荧光在胚胎发生过程中缺失,而部分 gfp dsRNA 注射的胚胎在胚胎发生后期开始显示 GFP 荧光。当 gfp dsRNA 被注射到携带 gfp 基因的母体蛹中时,RNAi 效应会传递到下一代的所有胚胎中,并持续到中幼虫阶段。从母体注射 dsRNA 在穿透效应和存活率方面比胚胎注射更有效。在最后龄幼虫中注射 gfp dsRNA 后,RNAi 效应在预蛹和蛹期以及成虫期持续存在。在这些敲低表型中,gfp 基因转录本明显减少。通过使用荧光标记的 dsRNA 表明,注射的 dsRNA 被内部器官吸收。内源性基因 Distal-less(Dll)的敲低导致了缺乏和畸形的 Dll 表达器官的典型表型,例如肢体和翅膀边缘的远端部分,而没有表现出脱靶效应。相比之下,dsRNA 注射的 RNAi 在中到晚期幼虫阶段似乎效果不佳。