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Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies

Abstract

RNA interference (RNAi) is an important means of eliminating mRNAs, but the intracellular location of RNA-induced silencing complex (RISC) remains unknown. We show here that Argonaute 2, a key component of RISC, is not randomly distributed but concentrates in mRNA decay centres that are known as cytoplasmic bodies. The localization of Argonaute 2 in decay centres is not altered by the presence or absence of small interfering RNAs or their targeted mRNAs. However, RNA is required for the integrity of cytoplasmic bodies because RNase eliminates Argonaute 2 localization. In addition, Argonaute 1, another Argonaute family member, is concentrated in cytoplasmic bodies. These results provide new insight into the mechanism of RNAi function.

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Figure 1: Localization of Ago2 in discrete foci within human cells.
Figure 2: Ago2 colocalizes and associates with Ago1.
Figure 3: Ago2 resides in sites of mRNA decay.
Figure 4: Ago2 localizes to cytoplasmic bodies in the presence of shRNA with its targeted mRNA, and requires RNA for mRNA decay centre localization.

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References

  1. Fire, A. et al. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391, 806–811 (1998).

    Article  CAS  Google Scholar 

  2. Hannon, G. J. RNA interference. Nature 418, 244–251 (2002).

    Article  CAS  Google Scholar 

  3. Liu, J., Carmell, M. A., Rivas, F. V., Marsden, C. G. & Hannon, G. J. Argonaute2 is the catalytic engine of mammalian RNAi. Science 305, 1437–1441 (2004).

    Article  CAS  Google Scholar 

  4. Pham, J. W., Pellino, J. L., Lee, Y. S., Carthew, R. W. & Sontheimer, E. J. A Dicer-2-dependent 80s complex cleaves targeted mRNAs during RNAi in Drosophila. Cell 117, 83–94 (2004).

    Article  CAS  Google Scholar 

  5. Gu, S. & Rossi, J. J. Uncoupling of RNAi from active translation in mammalian cells. RNA 11, 38–44 (2005).

    Article  CAS  Google Scholar 

  6. Bashkirov, V. I., Scherthan, H., Solinger, J. A., Buerstedde, J. M. & Heyer, W. D. A mouse cytoplasmic exoribonuclease (mXRN1p) with preference for G4 tetraplex substrates. J. Cell Biol. 136, 761–773 (1997).

    Article  CAS  Google Scholar 

  7. Cougot, N., Babajko, S. & Seraphin, B. Cytoplasmic foci are sites of mRNA decay in human cells. J. Cell Biol. 165, 31–40 (2004).

    Article  CAS  Google Scholar 

  8. Sheth, U. & Parker, R. Decapping and decay of messenger RNA occur in cytoplasmic processing bodies. Science 300, 805–808 (2003).

    Article  CAS  Google Scholar 

  9. Souret, F. F., Kastenmayer, J. P. & Green, P. J. AtXRN4 degrades mRNA in Arabidopsis and its substrates include selected miRNA targets. Mol. Cell 15, 173–183 (2004).

    Article  CAS  Google Scholar 

  10. Gazzani, S., Lawrenson, T., Woodward, C., Headon, D. & Sablowski, R. A link between mRNA turnover and RNA interference in Arabidopsis. Science 306, 1046–1048 (2004).

    Article  CAS  Google Scholar 

  11. Orban, T. I. & Izaurralde, E. Decay of mRNAs targeted by RISC requires XRN1, the Ski complex, and the exosome. RNA 459–469 (2005).

  12. Meister, G. & Tuschl, T. Mechanisms of gene silencing by double-stranded RNA. Nature 431, 343–349 (2004).

    Article  CAS  Google Scholar 

  13. Meister, G. et al. Human Argonaute2 mediates RNA cleavage targeted by miRNAs and siRNAs. Mol. Cell 15, 185–197 (2004).

    Article  CAS  Google Scholar 

  14. Eystathioy, T. et al. The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies. RNA 9, 1171–1173 (2003).

    Article  CAS  Google Scholar 

  15. Sen, G., Wehrman, T. S., Myers, J. W. & Blau, H. M. Restriction enzyme-generated siRNA (REGS) vectors and libraries. Nature Genet. 36, 183–189 (2004).

    Article  CAS  Google Scholar 

  16. Teixeira, D., Sheth, U., Valencia-Sanchez, M. A., Brengues, M. & Parker, R. Processing bodies require RNA for assembly and contain nontranslating mRNAs. RNA 371–382 (2005).

  17. Yekta, S., Shih, I. H. & Bartel, D. P. MicroRNA-directed cleavage of HOXB8 mRNA. Science 304, 594–596 (2004).

    Article  CAS  Google Scholar 

  18. Jing, Q. et al. Involvement of microRNA in AU-rich element-mediated mRNA instability. Cell 120, 623–634 (2005).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank T. Tuschl for the Flag-tagged Ago1 and Ago2 constructs, J. Lykke-Andersen for the Flag-tagged Dcp1a and Dcp2 constructs, and R. Wolkowicz for HEK 293 cells stably expressing the ecotropic receptor. We thank T. Wehrman for discussions and help with experiment design. This work was supported by a graduate fellowship from the Howard Hughes Medical Institute to G.L.S., and NIH grants AG09521, AG20961, HL65572 and HD18179, Ellison Medical Foundation Grant AG-33-0817, and support from the Baxter Foundation to H.M.B.

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Correspondence to Helen M. Blau.

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Sen, G., Blau, H. Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies. Nat Cell Biol 7, 633–636 (2005). https://doi.org/10.1038/ncb1265

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