Nuclear reorganization and homologous chromosome pairing during meiotic prophase require C. elegans chk-2

  1. Amy J. MacQueen and
  2. Anne M. Villeneuve1
  1. Department of Developmental Biology, Stanford University School of Medicine, Stanford, California 94305-5329, USA

Abstract

Analysis of mutants defective in meiotic chromosome pairing has uncovered a role for Caenorhabditis elegans chk-2 in initial establishment of pairing between homologous chromosomes during early meiotic prophase. chk-2 is also required for the major spatial reorganization of nuclei that normally accompanies the onset of pairing, suggesting a mechanistic coupling of these two events. Despite failures in pairing, nuclear reorganization, and crossover recombination, chk-2 mutants undergo many other aspects of meiotic chromosome morphogenesis and complete gametogenesis. Althoughchk-2 encodes a C. elegans ortholog of the Cds1/Chk2 checkpoint protein kinases, germ-line nuclei in chk-2 mutants are competent to arrest proliferation in response to replication inhibition and to trigger DNA damage checkpoint responses to ionizing radiation. However, chk-2 mutants are defective in triggering the pachytene DNA damage checkpoint in response to an intermediate block in the meiotic recombination pathway, suggesting thatchk-2 is required either for initiation of meiotic recombination or for monitoring a specific subset of DNA damage lesions. We propose that chk-2 functions during premeiotic S phase to enable chromosomes to become competent for subsequent meiotic prophase events and/or to coordinate replication with entry into prophase.

Keywords

Footnotes

  • 1 Corresponding author.

  • E-MAIL villen{at}cmgm.stanford.edu; FAX (650) 725-7739.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.902601.

    • Received April 11, 2001.
    • Accepted May 17, 2001.
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