LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans
Autor: | Eric A. Miska, Nicolas J. Lehrbach, Anthony Bugaut, Kenneth J. Murfitt, Helen L. Lightfoot, Javier Armisen, Shankar Balasubramanian |
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Rok vydání: | 2009 |
Předmět: |
Ribonuclease III
Cellular differentiation Molecular Sequence Data Regulator LIN28 Models Biological DNA-binding protein Article Animals Genetically Modified 03 medical and health sciences 0302 clinical medicine Structural Biology Sequence Homology Nucleic Acid microRNA Animals RNA Processing Post-Transcriptional Caenorhabditis elegans Caenorhabditis elegans Proteins Molecular Biology Polymerase 030304 developmental biology Genetics 0303 health sciences Base Sequence biology fungi Cell Differentiation biology.organism_classification Nucleotidyltransferases Cell biology Repressor Proteins MicroRNAs Gene Expression Regulation 030220 oncology & carcinogenesis biology.protein Dicer |
Zdroj: | Nature structural & molecular biology |
ISSN: | 1545-9985 1545-9993 |
DOI: | 10.1038/nsmb.1675 |
Popis: | Developmental expression of the microRNA let-7 is tightly regulated in many animals, and turnover has been linked to LIN-28 and uridylation in mammals. This regulation is now shown to be conserved in Caenorhabditis elegans, and PUP-2 is shown to be a uridylase that is specifically recruited to let-7 in a LIN-28–dependent manner. 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. |
Databáze: | OpenAIRE |
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