4.5 Article

LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 16, Issue 10, Pages 1016-U27

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.1675

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Funding

  1. Wellcome Trust
  2. Biotechnology and Biological Sciences Research Council (UK)
  3. Cancer Research UK
  4. Cancer Research UK [6934] Funding Source: researchfish

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The let-7 microRNA ( miRNA) is an ultraconserved regulator of stem cell differentiation and developmental timing and a candidate tumor suppressor. Here we show that LIN-28 and the poly( U) polymerase PUP-2 regulate let-7 processing in Caenorhabditis elegans. We demonstrate that lin-28 is necessary and sufficient to block let-7 activity in vivo; LIN-28 directly binds let-7 pre-miRNA to prevent Dicer processing. Moreover, we have identified a poly( U) polymerase, PUP-2, which regulates the stability of LIN-28 blockaded let-7 pre-miRNA and contributes to LIN-28-dependent regulation of let-7 during development. We show that PUP-2 and LIN-28 interact directly, and that LIN-28 stimulates uridylation of let-7 pre-miRNA by PUP-2 in vitro. Our results demonstrate that LIN-28 and let-7 form an ancient regulatory switch, conserved from nematodes to humans, and provide insight into the mechanism of LIN-28 action in vivo. Uridylation by a PUP-2 ortholog might regulate let-7 and additional miRNAs in other species. Given the roles of Lin28 and let-7 in stem cell and cancer biology, we propose that such poly( U) polymerases are potential therapeutic targets.

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