4.8 Article

The Decapping Scavenger Enzyme DCS-1 Controls MicroRNA Levels in Caenorhabditis elegans

期刊

MOLECULAR CELL
卷 50, 期 2, 页码 281-287

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2013.02.023

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资金

  1. NIH National Center for Research Resources (NCRR)
  2. Fonds de la recherche en sante du Quebec Scholarship
  3. Canadian Institutes of Health Research (CIHR)
  4. European Research Council (miRTurn) [ERC 2419845]
  5. Swiss National Science Foundation [SNF 31003A_127052]
  6. Friedrich Miescher Institute
  7. Novartis Research Foundation
  8. US NIH [R01 GM24028]
  9. Swiss National Science Foundation (SNF) [31003A_127052] Funding Source: Swiss National Science Foundation (SNF)

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In metazoans, microRNAs play a critical role in the posttranscriptional regulation of genes required for cell proliferation and differentiation. MicroRNAs themselves are regulated by a multitude of mechanisms influencing their transcription and posttranscriptional maturation. However, there is only sparse knowledge on pathways regulating the mature, functional form of microRNA. Here, we uncover the implication of the decapping scavenger protein DCS-1 in the control of microRNA turnover. In Caenorhabditis elegans, mutations in dcs-1 increase the levels of functional microRNAs. We demonstrate that DCS-1 interacts with the exonuclease XRN-1 to promote microRNA degradation in an independent manner from its known decapping scavenger activity, establishing two molecular functions for DCS-1. Our findings thus indicate that DCS-1 is part of a degradation complex that performs microRNA turnover in animals.

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