Elkayam Elad, Faehnle Christopher R, Morales Marjorie, Sun Jingchuan, Li Huilin, Joshua-Tor Leemor
Keck Structural Biology Laboratory, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Keck Structural Biology Laboratory, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Undergraduate Research Program, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Mol Cell. 2017 Aug 17;67(4):646-658.e3. doi: 10.1016/j.molcel.2017.07.007. Epub 2017 Aug 3.
In miRNA-mediated gene silencing, the physical interaction between human Argonaute (hAgo) and GW182 (hGW182) is essential for facilitating the downstream silencing of the targeted mRNA. GW182 can interact with hAgo via three of the GW/WG repeats in its Argonaute-binding domain: motif-1, motif-2, and the hook motif. The structure of hAgo1 in complex with the hook motif of hGW182 reveals a "gate"-like interaction that is critical for GW182 docking into one of hAgo1's tryptophan-binding pockets. We show that hAgo1 and hAgo2 have a single GW182-binding site and that miRNA binding increases hAgo's affinity to GW182. With target binding occurring rapidly, this ensures that only mature RISC would be recruited for silencing. Finally, we show that hGW182 can recruit up to three copies of hAgo via its three GW motifs. This may explain the observed cooperativity in miRNA-mediated gene silencing.
在微小RNA(miRNA)介导的基因沉默过程中,人类AGO蛋白(hAgo)与GW182蛋白(hGW182)之间的物理相互作用对于促进靶标信使核糖核酸(mRNA)的下游沉默至关重要。GW182可通过其AGO蛋白结合结构域中的三个GW/WG重复序列与hAgo相互作用:基序-1、基序-2和钩状基序。hAgo1与hGW182钩状基序的复合物结构揭示了一种“门”样相互作用,这对于GW182对接进入hAgo1的一个色氨酸结合口袋至关重要。我们发现hAgo1和hAgo2具有单一的GW182结合位点,并且miRNA结合会增加hAgo对GW182的亲和力。由于靶标结合迅速发生,这确保了只有成熟的RNA诱导沉默复合体(RISC)会被招募用于沉默。最后,我们发现hGW182可通过其三个GW基序招募多达三个拷贝的hAgo。这可能解释了在miRNA介导的基因沉默中观察到的协同作用。