4.8 Article

LIN41 Post-transcriptionally Silences mRNAs by Two Distinct and Position-Dependent Mechanisms

Journal

MOLECULAR CELL
Volume 65, Issue 3, Pages 476-+

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2016.12.010

Keywords

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Funding

  1. Swiss National Science Foundation [31003A_149402, 31003A_163447]
  2. NCCR RNA Disease
  3. European Union [241985]
  4. Novartis Research Foundation through the FMI
  5. EMBO [ALTF 95-2015]
  6. European Commission [GA-2013-609409]
  7. FMI
  8. NIH Office of Research Infrastructure Programs [P40 OD010440]
  9. Swiss National Science Foundation (SNF) [31003A_149402, 31003A_163447] Funding Source: Swiss National Science Foundation (SNF)
  10. European Research Council (ERC) [241985] Funding Source: European Research Council (ERC)

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The RNA-binding protein (RBP) LIN41, also known as LIN-41 or TRIM71, is a key regulator of animal development, but its physiological targets and molecular mechanism of action are largely elusive. Here we find that this RBP has two distinct mRNA-silencing activities. Using genome-wide ribosome profiling, RNA immunoprecipitation, and in vitro-binding experiments, we identify four mRNAs, each encoding a transcription factor or cofactor, as direct physiological targets of C. elegans LIN41. LIN41 silences three of these targets through their 30 UTRs, but it achieves isoform-specific silencing of one target, lin-29A, through its unique 50 UTR. Whereas the 30 UTR targets mab-10, mab-3, and dmd-3 undergo transcript degradation, lin-29A experiences translational repression. Through binding site transplantation experiments, we demonstrate that it is the location of the LIN41-binding site that specifies the silencing mechanism. Such position-dependent dual activity may, when studied more systematically, emerge as a feature shared by other RBPs.

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