Roles of the HEAT repeat proteins Utp10 and Utp20 in 40S ribosome maturation

  1. Christophe Dez1,3,
  2. Mensur Dlakić2, and
  3. David Tollervey1
  1. 1Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, Scotland
  2. 2Department of Microbiology, Montana State University, Bozeman, Montana 59717-3520, USA

Abstract

A family of HEAT-repeat containing ribosome synthesis factors was previously identified in Saccharomyces cerevisiae. We report the detailed characterization of two of these factors, Utp10 and Utp20, which were initially identified as components of the small subunit processome. Coprecipitation analyses confirmed the association of Utp10 and Utp20 with U3 snoRNA and the early pre-rRNA processing intermediates. Particularly strong association was seen with aberrant processing intermediates, which may help target these RNAs for degradation. Genetic depletion of either protein inhibited the early pre-rRNA processing steps in 18S rRNA maturation but had little effect on pre-rRNA transcription or synthesis of the 25S or 5.8S rRNAs. The absence of the poly(A) polymerase Trf5, a component of the TRAMP5 complex and exosome cofactor, led to stabilization of the aberrant 23S RNA in strains depleted of Utp10 or Utp20. In the case of Utp10, 20S pre-rRNA synthesis was also modestly increased by this loss of surveillance activity.

Keywords

Footnotes

  • 3 Present address: Laboratoire de Biologie Moléculaire Eucaryote, CNRS-Université Paul Sabatier, IFR109, Toulouse, France.

  • Reprint requests to: David Tollervey, Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings, Edinburgh EH9 3JR, Scotland; e-mail: d.tollervey{at}ed.ac.uk; fax: 44-131-650-7040.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.609807.

    • Received April 27, 2007.
    • Accepted June 7, 2007.
  • Freely available online through the open access option.

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