MEI-1/MEI-2 katanin-like microtubule severing activity is required for Caenorhabditis elegans meiosis

  1. Martin Srayko1,
  2. Dan W. Buster2,
  3. Omar A. Bazirgan2,
  4. Francis J. McNally2, and
  5. Paul E. Mains1,3
  1. 1Department of Biochemistry and Molecular Biology, Genes and Development Research Group, University of Calgary, Calgary, Alberta, T2N 4N1 Canada; 2Section of Molecular and Cellular Biology, University of California, Davis, California 95616 USA

Abstract

The Caenorhabditis elegans meiotic spindle is morphologically distinct from the first mitotic spindle, yet both structures form in the same cytoplasm ∼20 minutes apart. Themei-1 and mei-2 genes of C. elegans are required for the establishment of the oocyte meiotic spindle but are not required for mitotic spindle function. mei-1 encodes an AAA ATPase family member with similarity to the p60 catalytic subunit of the heterodimeric sea urchin microtubule-severing protein, katanin. We report that mei-2 encodes a 280-amino acid protein containing a region similar to the p80-targeting subunit of katanin. MEI-1 and MEI-2 antibodies decorate the polar ends of meiotic spindle microtubules and meiotic chromatin. We find that the subcellular location of MEI-2 depends on wild-type mei-1 activity and vice versa. These experiments, combined with MEI-1 and MEI-2's similarity to p60 and p80 katanin, suggest that the C. elegans proteins function as a complex. In support of this idea, MEI-1 and MEI-2 physically associate in HeLa cells. Furthermore, co-expression of MEI-1 and MEI-2 in HeLa cells results in the disassembly of microtubules. These data lead us to conclude that MEI-1/MEI-2 microtubule-severing activity is required for meiotic spindle organization in C. elegans.

Keywords

Footnotes

  • 3 Corresponding author.

  • E-MAIL mains{at}ucalgary.ca; FAX (403) 270-0737.

    • Received February 24, 2000.
    • Accepted March 20, 2000.
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