1. Max Delbrück Center for Molecular Medicine, Robert-Rössle Str. 10, D-13125 Berlin, Germany
2. Department of Statistics, 15 University Gardens, University of Glasgow, Glasgow, G12 8QQ, UK
3. These authors contributed equally to this work.

Correspondence to: Matthias Selbach¹Nikolaus Rajewsky¹ Correspondence and requests for materials should be addressed to M.S. (Email: matthias.selbach@mdc-berlin.de) and N.R. (Email: rajewsky@mdc-berlin.de).

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.

1. Max Delbrück Center for Molecular Medicine, Robert-Rössle Str. 10, D-13125 Berlin, Germany
2. Department of Statistics, 15 University Gardens, University of Glasgow, Glasgow, G12 8QQ, UK
3. These authors contributed equally to this work.

Correspondence to: Matthias Selbach¹Nikolaus Rajewsky¹ Correspondence and requests for materials should be addressed to M.S. (Email: matthias.selbach@mdc-berlin.de) and N.R. (Email: rajewsky@mdc-berlin.de).

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