KREPA4, an RNA binding protein essential for editosome integrity and survival of Trypanosoma brucei

  1. Reza Salavati1,2,3,
  2. Nancy Lewis Ernst1,
  3. Jeff O'Rear1,
  4. Troy Gilliam1,
  5. Salvador Tarun, Jr.1, and
  6. Kenneth Stuart1,2
  1. 1Seattle Biomedical Research Institute, Seattle, Washington 98109, USA
  2. 2Department of Pathobiology, University of Washington, Seattle, Washington 98195, USA

Abstract

The 20S editosome, a multiprotein complex, catalyzes the editing of most mitochondrial mRNAs in trypanosomatids by uridylate insertion and deletion. RNAi mediated inactivation of expression of KREPA4 (previously TbMP24), a component of the 20S editosome, in procyclic form Trypanosoma brucei resulted in inhibition of cell growth, loss of RNA editing, and disappearance of 20S editosomes. Levels of MRP1 and REAP-1 proteins, which may have roles in editing but are not editosome components, were unaffected. Tagged KREPA4 protein is incorporated into 20S editosomes in vivo with no preference for either insertion or deletion subcomplexes. Consistent with its S1-like motif, recombinant KREPA4 protein binds synthetic gRNA with a preference for the 3′ oligo (U) tail. These data suggest that KREPA4 is an RNA binding protein that may be specific for the gRNA Utail and also is important for 20S editosome stability.

Keywords

Footnotes

  • 3

    3 Present address: McGill University, Institute of Parasitology, Montreal, Quebec H9X 3V9, Canada.

  • Reprint requests to: Kenneth Stuart, Seattle Biomedical Research Institute, 307 Westlake Ave. N, Suite 500, Seattle, WA 98109-5219, USA; e-mail: ken.stuart{at}sbri.org; fax: (206) 256-7229.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.2244106.

    • Received September 29, 2005.
    • Accepted February 8, 2006.
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