Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.
Mol Cell. 2012 Sep 14;47(5):746-54. doi: 10.1016/j.molcel.2012.07.014. Epub 2012 Aug 16.
Ingested dsRNAs trigger RNA interference (RNAi) in many invertebrates, including the nematode Caenorhabditis elegans. Here we show that the C. elegans apical intestinal membrane protein SID-2 is required in C. elegans for the import of ingested dsRNA and that, when expressed in Drosophila S2 cells, SID-2 enables the uptake of dsRNAs. SID-2-dependent dsRNA transport requires an acidic extracellular environment and is selective for dsRNAs with at least 50 base pairs. Through structure-function analysis, we identify several SID-2 regions required for this activity, including three extracellular, positively charged histidines. Finally, we find that SID-2-dependent transport is inhibited by drugs that interfere with vesicle transport. Therefore, we propose that environmental dsRNAs are imported from the acidic intestinal lumen by SID-2 via endocytosis and are released from internalized vesicles in a secondary step mediated by the dsRNA channel SID-1. Similar multistep mechanisms may underlie the widespread observations of environmental RNAi.
摄入的双链 RNA 在许多无脊椎动物中引发 RNA 干扰 (RNAi),包括线虫秀丽隐杆线虫。在这里,我们表明线虫顶端肠膜蛋白 SID-2 在线虫中需要将摄入的双链 RNA 导入,并且当在果蝇 S2 细胞中表达时,SID-2 能够摄取双链 RNA。SID-2 依赖性双链 RNA 转运需要酸性细胞外环境,并且对至少 50 个碱基对的双链 RNA 具有选择性。通过结构功能分析,我们确定了几个 SID-2 区域需要这种活性,包括三个细胞外的、带正电荷的组氨酸。最后,我们发现 SID-2 依赖性运输被干扰囊泡运输的药物抑制。因此,我们提出环境双链 RNA 通过 SID-2 通过内吞作用从酸性肠腔中摄取,并在由双链 RNA 通道 SID-1 介导的后续步骤中从内化的囊泡中释放。类似的多步机制可能是广泛观察到的环境 RNAi 的基础。