| Literature DB >> 28431233 |
Thomas Treiber1, Nora Treiber1, Uwe Plessmann2, Simone Harlander1, Julia-Lisa Daiß1, Norbert Eichner1, Gerhard Lehmann1, Kevin Schall1, Henning Urlaub2, Gunter Meister3.
Abstract
During microRNA (miRNA) biogenesis, two endonucleolytic reactions convert stem-loop-structured precursors into mature miRNAs. These processing steps can be posttranscriptionally regulated by RNA-binding proteins (RBPs). Here, we have used a proteomics-based pull-down approach to map and characterize the interactome of a multitude of pre-miRNAs. We identify ∼180 RBPs that interact specifically with distinct pre-miRNAs. For functional validation, we combined RNAi and CRISPR/Cas-mediated knockout experiments to analyze RBP-dependent changes in miRNA levels. Indeed, a large number of the investigated candidates, including splicing factors and other mRNA processing proteins, have effects on miRNA processing. As an example, we show that TRIM71/LIN41 is a potent regulator of miR-29a processing and its inactivation directly affects miR-29a targets. We provide an extended database of RBPs that interact with pre-miRNAs in extracts of different cell types, highlighting a widespread layer of co- and posttranscriptional regulation of miRNA biogenesis.Entities:
Keywords: LIN28; RNA binding proteins; RNA processing; RNA pull-down; TRIM71; ZC3H10; ZC3H7; microRNA-guided gene silencing; regulation of microRNA biogenesis; siRNA pool
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Year: 2017 PMID: 28431233 DOI: 10.1016/j.molcel.2017.03.014
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970