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Posttranscriptional crossregulation between Drosha and DGCR8.

Authors
  • J, Han
  • Js, Pedersen
  • Sc, Kwon
  • Cd, Belair
  • Yk, Kim
  • Kh, Yeom
  • Wy, Yang
  • David Haussler
  • R, Blelloch
  • Vn, Kim
Type
Published Article
Journal
Cell
Publisher
Elsevier
Publication Date
Jan 16, 2009
Volume
136
Issue
1
Pages
75–75
Identifiers
DOI: 10.1016/j.cell.2008.10.053
Source
UCSC Bioengineering biomedical-ucsc
License
Green

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.

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