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Journal Article

Dicer-dependent and -independent Argonaute2 Protein Interaction Networks in Mammalian Cells

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Frohn,  Anne
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Eberl,  H. Christian
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Mann,  Matthias
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Meister,  Gunter
Former Research Groups, Max Planck Institute of Biochemistry, Max Planck Society;

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Citation

Frohn, A., Eberl, H. C., Stoehr, J., Glasmacher, E., Ruedel, S., Heissmeyer, V., et al. (2012). Dicer-dependent and -independent Argonaute2 Protein Interaction Networks in Mammalian Cells. MOLECULAR & CELLULAR PROTEOMICS, 11(11), 1442-1456. doi:10.1074/mcp.M112.017756.


Cite as: https://hdl.handle.net/11858/00-001M-0000-000E-AC2C-2
Abstract
Argonaute (Ago) proteins interact with small regulatory RNAs such as microRNAs (miRNAs) and facilitate gene-silencing processes. miRNAs guide Ago proteins to specific mRNAs leading to translational silencing or mRNA decay. In order to understand the mechanistic details of miRNA function, it is important to characterize Ago protein interactors. Although several proteomic studies have been performed, it is not clear how the Ago interactome changes on miRNA or mRNA binding. Here, we report the analysis of Ago protein interactions in miRNA-containing and miRNA-depleted cells. Using stable isotope labeling in cell culture in conjunction with Dicer knock out mouse embryonic fibroblasts, we identify proteins that interact with Ago2 in the presence or the absence of Dicer. In contrast to our current view, we find that Ago-mRNA interactions can also take place in the absence of miRNAs. Our proteomics approach provides a rich resource for further functional studies on the cellular roles of Ago proteins. Molecular & Cellular Proteomics 11: 10.1074/mcp.M112.017756, 1442-1456, 2012.