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Posttranscriptional Crossregulation between Drosha and DGCR8

Cited 330 time in Web of Science Cited 347 time in Scopus
Authors

Han, Jinju; Pedersen, Jakob S.; Kwon, S. Chul; Belair, Cassandra D.; Kim, Young-Kook; Yeom, Kyu-Hyeon; Yang, Woo-Young; Haussler, David; Blelloch, Robert; Kim, V. Narry

Issue Date
2009-01
Publisher
Cell Press
Citation
Cell, Vol.136 No.1, pp.75-84
Abstract
The Drosha-DGCR8 complex, also known as Microprocessor, is essential for microRNA (miRNA) maturation. Drosha functions as the catalytic subunit, while DGCR8 (also known as Pasha) recognizes the RNA substrate. Although the action mechanism of this complex has been intensively studied, it remains unclear how Drosha and DGCR8 are regulated and if these proteins have any additional role(s) apart from miRNA processing. Here, we report that Drosha and DGCR8 regulate each other posttranscriptionally. The Drosha-DGCR8 complex cleaves the hairpin structures embedded in the DGCR8 mRNA and thereby destabilizes the mRNA. We further find that DGCR8 stabilizes the Drosha protein via protein-protein interaction. This crossregulation between Drosha and DGCR8 may contribute to the homeostatic control of miRNA biogenesis. Furthermore, microarray analyses suggest that a number of mRNAs may be downregulated in a Microprocessor-dependent, miRNA-independent manner. Our study reveals a previously unsuspected function of Microprocessor in mRNA stability control.
ISSN
0092-8674
URI
https://hdl.handle.net/10371/171928
DOI
https://doi.org/10.1016/j.cell.2008.10.053
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

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