Abstract
Animal microRNAs (miRNAs) regulate gene expression by inhibiting translation and/or by inducing degradation of target messenger RNAs. It is unknown how much translational control is exerted by miRNAs on a genome-wide scale. We used a new proteomic approach to measure changes in synthesis of several thousand proteins in response to miRNA transfection or endogenous miRNA knockdown. In parallel, we quantified mRNA levels using microarrays. Here we show that a single miRNA can repress the production of hundreds of proteins, but that this repression is typically relatively mild. A number of known features of the miRNA-binding site such as the seed sequence also govern repression of human protein synthesis, and we report additional target sequence characteristics. We demonstrate that, in addition to downregulating mRNA levels, miRNAs also directly repress translation of hundreds of genes. Finally, our data suggest that a miRNA can, by direct or indirect effects, tune protein synthesis from thousands of genes.
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References
Ambros, V. The functions of animal microRNAs. Nature 431, 350–355 (2004)
Bartel, D. P. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116, 281–297 (2004)
Bushati, N. & Cohen, S. M. microRNA functions. Annu. Rev. Cell Dev. Biol. 23, 175–205 (2007)
He, L. & Hannon, G. J. MicroRNAs: small RNAs with a big role in gene regulation. Nature Rev. Genet. 5, 522–531 (2004)
Lai, E. C. miRNAs: whys and wherefores of miRNA-mediated regulation. Curr. Biol. 15, R458–R460 (2005)
Filipowicz, W., Bhattacharyya, S. N. & Sonenberg, N. Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? Nature Rev. Genet. 9, 102–114 (2008)
Shyu, A. B., Wilkinson, M. F. & van Hoof, A. Messenger RNA regulation: to translate or to degrade. EMBO J. 27, 471–481 (2008)
Mathonnet, G. et al. MicroRNA inhibition of translation initiation in vitro by targeting the cap-binding complex eIF4F. Science 317, 1764–1767 (2007)
Thermann, R. & Hentze, M. W. Drosophila miR2 induces pseudo-polysomes and inhibits translation initiation. Nature 447, 875–878 (2007)
Wakiyama, M., Takimoto, K., Ohara, O. & Yokoyama, S. Let-7 microRNA-mediated mRNA deadenylation and translational repression in a mammalian cell-free system. Genes Dev. 21, 1857–1862 (2007)
Liu, J. Control of protein synthesis and mRNA degradation by microRNAs. Curr. Opin. Cell. Biol. 20, 214–221 (2008)
Lim, L. P. et al. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature 433, 769–773 (2005)
Bentwich, I. Prediction and validation of microRNAs and their targets. FEBS Lett. 579, 5904–5910 (2005)
Hofacker, I. L. How microRNAs choose their targets. Nature Genet. 39, 1191–1192 (2007)
Rajewsky, N. microRNA target predictions in animals. Nature Genet. 38 (Suppl). S8–S13 (2006)
Sethupathy, P., Megraw, M. & Hatzigeorgiou, A. G. A guide through present computational approaches for the identification of mammalian microRNA targets. Nature Methods 3, 881–886 (2006)
Beitzinger, M. et al. Identification of human microRNA targets from isolated argonaute protein complexes. RNA Biol. 4, 76–84 (2007)
Easow, G., Teleman, A. A. & Cohen, S. M. Isolation of microRNA targets by miRNP immunopurification. RNA 13, 1198–1204 (2007)
Karginov, F. V. et al. A biochemical approach to identifying microRNA targets. Proc. Natl Acad. Sci. USA 104, 19291–19296 (2007)
Hendrickson, D. G. et al. Systematic identification of mRNAs recruited to argonaute 2 by specific microRNAs and corresponding changes in transcript abundance. PLoS ONE 3, e2126 (2008)
Aleman, L. M., Doench, J. & Sharp, P. A. Comparison of siRNA-induced off-target RNA and protein effects. RNA 13, 385–395 (2007)
Vinther, J. et al. Identification of miRNA targets with stable isotope labeling by amino acids in cell culture. Nucleic Acids Res. 34, e107 (2006)
Stefani, G. & Slack, F. J. Small non-coding RNAs in animal development. Nature Rev. Mol. Cell Biol. 9, 219–230 (2008)
Mann, M. Functional and quantitative proteomics using SILAC. Nature Rev. Mol. Cell Biol. 7, 952–958 (2006)
Ong, S. E. et al. Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics. Mol. Cell. Proteomics 1, 376–386 (2002)
Schwanhaeusser, B., Gossen, M., Dittmar, G. & Selbach, M. Global analysis of cellular protein translation by pulsed SILAC. Proteomics (in the press)
Milner, E., Barnea, E., Beer, I. & Admon, A. The turnover kinetics of major histocompatibility complex peptides of human cancer cells. Mol. Cell. Proteomics 5, 357–365 (2006)
Pratt, J. M. et al. Dynamics of protein turnover, a missing dimension in proteomics. Mol. Cell. Proteomics 1, 579–591 (2002)
Lam, Y. W., Lamond, A. I., Mann, M. & Andersen, J. S. Analysis of nucleolar protein dynamics reveals the nuclear degradation of ribosomal proteins. Curr. Biol. 17, 749–760 (2007)
Cox, J. & Mann, M. Is proteomics the new genomics? Cell 130, 395–398 (2007)
Cravatt, B. F., Simon, G. M. & Yates, J. R. The biological impact of mass-spectrometry-based proteomics. Nature 450, 991–1000 (2007)
Domon, B. & Aebersold, R. Mass spectrometry and protein analysis. Science 312, 212–217 (2006)
Landgraf, P. et al. A mammalian microRNA expression atlas based on small RNA library sequencing. Cell 129, 1401–1414 (2007)
Sood, P. et al. Cell-type-specific signatures of microRNAs on target mRNA expression. Proc. Natl Acad. Sci. USA 103, 2746–2751 (2006)
Nielsen, C. B. et al. Determinants of targeting by endogenous and exogenous microRNAs and siRNAs. RNA 13, 1894–1910 (2007)
Grimson, A. et al. MicroRNA targeting specificity in mammals: determinants beyond seed pairing. Mol. Cell 27, 91–105 (2007)
Haley, B. & Zamore, P. D. Kinetic analysis of the RNAi enzyme complex. Nature Struct. Mol. Biol. 11, 599–606 (2004)
Martinez, J. & Tuschl, T. RISC is a 5′ phosphomonoester-producing RNA endonuclease. Genes Dev. 18, 975–980 (2004)
Schwarz, D. S. et al. Designing siRNA that distinguish between genes that differ by a single nucleotide. PLoS Genet. 2, e140 (2006)
Vasudevan, S., Tong, Y. & Steitz, J. A. Switching from repression to activation: microRNAs can up-regulate translation. Science 318, 1931–1934 (2007)
Doench, J. G., Petersen, C. P. & Sharp, P. A. siRNAs can function as miRNAs. Genes Dev. 17, 438–442 (2003)
Stenvang, J. et al. The utility of LNA in microRNA-based cancer diagnostics and therapeutics. Semin. Cancer Biol. 18, 89–102 (2008)
Wahlestedt, C. et al. Potent and nontoxic antisense oligonucleotides containing locked nucleic acids. Proc. Natl Acad. Sci. USA 97, 5633–5638 (2000)
Boyerinas, B. et al. Identification of let-7-regulated oncofetal genes. Cancer Res. 68, 2587–2591 (2008)
Kuster, B., Schirle, M., Mallick, P. & Aebersold, R. Scoring proteomes with proteotypic peptide probes. Nature Rev. Mol. Cell Biol. 6, 577–583 (2005)
Eulalio, A., Behm-Ansmant, I. & Izaurralde, E. P bodies: at the crossroads of post-transcriptional pathways. Nature Rev. Mol. Cell Biol. 8, 9–22 (2007)
Nottrott, S., Simard, M. J. & Richter, J. D. Human let-7a miRNA blocks protein production on actively translating polyribosomes. Nature Struct. Mol. Biol. 13, 1108–1114 (2006)
Ong, S. E. & Mann, M. A practical recipe for stable isotope labeling by amino acids in cell culture (SILAC). Nature Protocols 1, 2650–2660 (2007)
Elias, J. E. & Gygi, S. P. Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry. Nature Methods 4, 207–214 (2007)
Acknowledgements
We thank J. Cox and M. Mann for early access to the MaxQuant software package, N. D. Socci for discussions, S. Schmidt, G. Born and N. Huebner for the hybridizations at the MDC microarray facility, C. Sommer for technical assistance, M. Huska and M. Andrade-Navarro for setting up the pSILAC website, P. Sharp for a CXCR4 luciferase construct, M. Peter for the IMP-1 reporters, and the Bundesministerium für Bildung und Forschung for funding mass spectrometry instrumentation. R.K. gratefully acknowledges a DAAD scholarship for research stays at the MDC. pSILAC and microarray data can be queried at http://psilac.mdc-berlin.de.
Author Contributions M.S. and N.R. conceived, designed and supervised the experiments. B.S. and N.T. performed the wet lab experiments. M.S., Z.F., R.K. and N.R. analysed genome-wide data. M.S., R.K. and N.R. interpreted the data. M.S. and N.R. wrote the paper.
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Supplementary Information 1
The file contains Supplementary Methods, Supplementary Figures S1-S7 with Legends, Supplementary Table 1 and additional references. (PDF 2285 kb)
Supplementary Table 2
This table shows Gene ontology analysis of proteins which are predominately regulated at the level of translation. This file was originally omitted and was uploaded on 2nd April, 2009. (XLS 35 kb)
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Selbach, M., Schwanhäusser, B., Thierfelder, N. et al. Widespread changes in protein synthesis induced by microRNAs. Nature 455, 58–63 (2008). https://doi.org/10.1038/nature07228
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DOI: https://doi.org/10.1038/nature07228
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