4.8 Article

Multivalent Recruitment of Human Argonaute by GW182

Journal

MOLECULAR CELL
Volume 67, Issue 4, Pages 646-+

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2017.07.007

Keywords

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Funding

  1. NIH, National Institute of General Medical Sciences [GM-9064, IAA AGM-12005]
  2. Howard Hughes Medical Institute
  3. Office of Science, Office of Basic Energy Sciences, of the United States Department of Energy [DE-AC02-05CH11231]
  4. NIH R01 grant [GM111742]
  5. Cold Spring Harbor Laboratory Women in Science Award
  6. Direct For Biological Sciences
  7. Div Of Biological Infrastructure [1559816] Funding Source: National Science Foundation

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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.

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