A New, Expressed Multigene Family Containing a Hot Spot for Insertion of Retroelements Is Associated with Polymorphic Subtelomeric Regions of <i>Trypanosoma brucei</i>

  • Frédéric Bringaud
    Laboratoire de Parasitologie Moléculaire, Université Victor Segalen Bordeaux II, UMR-5016 CNRS, 33076 Bordeaux cedex, France
  • Nicolas Biteau
    Laboratoire de Parasitologie Moléculaire, Université Victor Segalen Bordeaux II, UMR-5016 CNRS, 33076 Bordeaux cedex, France
  • Sara E. Melville
    Molteno Institute for Parasitology, Department of Pathology, University of Cambridge, Cambridge CB2 1QP
  • Stéphanie Hez
    Laboratoire de Parasitologie Moléculaire, Université Victor Segalen Bordeaux II, UMR-5016 CNRS, 33076 Bordeaux cedex, France
  • Najib M. El-Sayed
    The Institute for Genomic Research, Rockville, Maryland 10850
  • Vanessa Leech
    Molteno Institute for Parasitology, Department of Pathology, University of Cambridge, Cambridge CB2 1QP
  • Matthew Berriman
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, United Kingdom
  • Neil Hall
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, United Kingdom
  • John E. Donelson
    Department of Biochemistry, University of Iowa, Iowa City, Iowa 52242
  • Théo Baltz
    Laboratoire de Parasitologie Moléculaire, Université Victor Segalen Bordeaux II, UMR-5016 CNRS, 33076 Bordeaux cedex, France

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説明

<jats:title>ABSTRACT</jats:title> <jats:p> We describe a novel gene family that forms clusters in subtelomeric regions of <jats:italic>Trypanosoma brucei</jats:italic> chromosomes and partially accounts for the observed clustering of retrotransposons. The <jats:italic>ingi</jats:italic> and ribosomal inserted mobile element (RIME) non-LTR retrotransposons share 250 bp at both extremities and are the most abundant putatively mobile elements, with about 500 copies per haploid genome. From cDNA clones and subsequently in the <jats:italic>T. brucei</jats:italic> genomic DNA databases, we identified 52 homologous gene and pseudogene sequences, 16 of which contain a RIME and/or <jats:italic>ingi</jats:italic> retrotransposon inserted at exactly the same relative position. Here these genes are called the <jats:italic>RHS</jats:italic> family, for retrotransposon hot spot. Comparison of the protein sequences encoded by <jats:italic>RHS</jats:italic> genes (21 copies) and pseudogenes (24 copies) revealed a conserved central region containing an ATP/GTP-binding motif and the RIME/ <jats:italic>ingi</jats:italic> insertion site. The RHS proteins share between 13 and 96% identity, and six subfamilies, <jats:italic>RHS1</jats:italic> to <jats:italic>RHS6</jats:italic> , can be defined on the basis of their divergent C-terminal domains. Immunofluorescence and Western blot analyses using RHS subfamily-specific immune sera show that RHS proteins are constitutively expressed and occur mainly in the nucleus. Analysis of Genome Survey Sequence databases indicated that the <jats:italic>Trypanosoma brucei</jats:italic> diploid genome contains about 280 <jats:italic>RHS</jats:italic> (pseudo)-genes. Among the 52 identified <jats:italic>RHS</jats:italic> (pseudo)genes, 48 copies are in three <jats:italic>RHS</jats:italic> clusters located in subtelomeric regions of chromosomes Ia and II and adjacent to the active bloodstream form expression site in <jats:italic>T. brucei</jats:italic> strain TREU927/4 GUTat10.1. <jats:italic>RHS</jats:italic> genes comprise the remaining sequence of the size-polymorphic “repetitive region” described for <jats:italic>T. brucei</jats:italic> chromosome I, and a homologous gene family is present in the <jats:italic>Trypanosoma cruzi</jats:italic> genome. </jats:p>

収録刊行物

  • Eukaryotic Cell

    Eukaryotic Cell 1 (1), 137-151, 2002-02

    American Society for Microbiology

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