Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Curr Biol. 2012 Oct 23;22(20):1938-43. doi: 10.1016/j.cub.2012.08.020. Epub 2012 Sep 13.
In the nematode C. elegans, RNAi silencing signals are efficiently taken up from the environment and transported between cells and tissues. Previous studies implicating endosomal proteins in systemic RNAi lack conclusive evidence. Here, we report the identification and characterization of SID-5, a C. elegans endosome-associated protein that is required for efficient systemic RNAi in response to both ingested and expressed double-stranded RNA (dsRNA). SID-5 is detected in cytoplasmic foci that partially colocalize with GFP fusions of late endosomal proteins RAB-7 and LMP-1. Furthermore, knockdown of various endosomal proteins similarly relocalizes both SID-5 and LMP-1::GFP. Consistent with a non-cell-autonomous function, intestine-specific SID-5 expression restored body wall muscle (bwm) target gene silencing in response to ingested dsRNA. Finally, we show that sid-5 is required for the previously described sid-1-independent transport of ingested RNAi triggers across the intestine. Together, these data demonstrate that an endosome-associated protein, SID-5, promotes the transport of RNAi silencing signals between cells. Furthermore, SID-5 acts differently than the previously described SID-1, SID-2, and SID-3 proteins, thus expanding the systemic RNAi pathway.
在秀丽隐杆线虫中,RNAi 沉默信号能从环境中高效摄取,并在细胞和组织间运输。先前的研究表明内体蛋白参与系统性 RNAi,但缺乏确凿的证据。在这里,我们鉴定并描述了 SID-5,一种线虫内体相关蛋白,它对系统性 RNAi 至关重要,能响应摄取和表达的双链 RNA(dsRNA)。SID-5 存在于细胞质斑点中,这些斑点与晚期内体蛋白 RAB-7 和 LMP-1 的 GFP 融合体部分共定位。此外,各种内体蛋白的敲低同样会重新定位 SID-5 和 LMP-1::GFP。与其非细胞自主功能一致,肠特异性 SID-5 表达恢复了对摄取 dsRNA 的体壁肌肉(bwm)靶基因沉默。最后,我们发现 sid-5 是先前描述的不需要 sid-1 的摄取 RNAi 触发物在肠内跨细胞运输所必需的。总之,这些数据表明,一种与内体相关的蛋白 SID-5 促进了 RNAi 沉默信号在细胞间的运输。此外,SID-5 的作用不同于先前描述的 SID-1、SID-2 和 SID-3 蛋白,从而扩展了系统性 RNAi 途径。