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  4. Reduced Expression of Ribosomal Proteins Relieves MicroRNA-Mediated Repression

Reduced Expression of Ribosomal Proteins Relieves MicroRNA-Mediated Repression

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Author(s)
Janas, Maja M.
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Love, Tara
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Harris, Abigail S.
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Stevenson, Kristen
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Semmelmann, Karlheinz
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Shaffer, Jonathan M.
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Chen, Po-Hao
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Doench, John G.
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Yerramilli, Subrahmanyam V.B.K.
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Neuberg, Donna S.
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Date Issued
April 2012
Journal
Molecular Cell
Publisher
Elsevier B.V.
Citation
Janas, Maja M., Eric Wang, Tara Love, Abigail S. Harris, Kristen Stevenson, Karlheinz Semmelmann, Jonathan M. Shaffer, et al. “Reduced Expression of Ribosomal Proteins Relieves MicroRNA-Mediated Repression.” Molecular Cell 46, no. 2 (April 2012): 171-186. © 2012 Elsevier.
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Final published version
Abstract
MicroRNAs (miRNAs) regulate physiological and pathological processes by inducing posttranscriptional repression of target messenger RNAs (mRNAs) via incompletely understood mechanisms. To discover factors required for human miRNA activity, we performed an RNAi screen using a reporter cell line of miRNA-mediated repression of translation initiation. We report that reduced expression of ribosomal protein genes (RPGs) dissociated miRNA complexes from target mRNAs, leading to increased polysome association, translation, and stability of miRNA-targeted mRNAs relative to untargeted mRNAs. RNA sequencing of polysomes indicated substantial overlap in sets of genes exhibiting increased or decreased polysomal association after Argonaute or RPG knockdowns, suggesting similarity in affected pathways. miRNA profiling of monosomes and polysomes demonstrated that miRNAs cosediment with ribosomes. RPG knockdowns decreased miRNAs in monosomes and increased their target mRNAs in polysomes. Our data show that most miRNAs repress translation and that the levels of RPGs modulate miRNA-mediated repression of translation initiation.
MIT Department
Massachusetts Institute of Technology. Department of Biology
Koch Institute for Integrative Cancer Research at MIT
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/83590
DOI of Published Version
https://doi.org/10.1016/j.molcel.2012.04.008
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