• Title of article

    Posttranscriptional Crossregulation between Drosha and DGCR8

  • Author/Authors

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

  • Issue Information
    هفته نامه با شماره پیاپی سال 2009
  • Pages
    10
  • From page
    75
  • To page
    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.
  • Journal title
    CELL
  • Serial Year
    2009
  • Journal title
    CELL
  • Record number

    1019579