Telomere-mediated chromosome pairing during meiosis in budding yeast

  1. Beth Rockmill1 and
  2. G. Shirleen Roeder1,2,3,4
  1. 1Howard Hughes Medical Institute, 2Department of Molecular, Cellular and Developmental Biology and 3Department of Genetics, Yale University, New Haven, Connecticut 06520-8103 USA

Abstract

Certain haploid strains of Saccharomyces cerevisiae can undergo meiosis, but meiotic prophase progression and subsequent nuclear division are delayed if these haploids carry an extra chromosome (i.e., are disomic). Observations indicate that interactions between homologous chromosomes cause a delay in meiotic prophase, perhaps to allow time for interhomolog interactions to be completed. Analysis of meiotic mutants demonstrates that the relevant aspect of homolog recognition is independent of meiotic recombination and synaptonemal complex formation. A disome in which the extra chromosome is circular sporulates without a delay, indicating that telomeres are important for homolog recognition. Consistent with this hypothesis, fluorescent in situ hybridization demonstrates that a circular chromosome has a reduced capacity to pair with its homolog, and a telomere-associated meiotic protein (Ndj1) is required to delay sporulation in disomes. A circular dimer containing two copies of the same chromosome delays meiosis to the same extent as two linear homologs, implying that physical proximity bypasses the requirement for telomeres in homolog pairing. Analysis of a disome carrying two linear permuted chromosomes suggests that even nonhomologous chromosome ends can promote homolog pairing to a limited extent. We speculate that telomere-mediated chromosome movement and/or telomere clustering promote homolog pairing.

Keywords

Footnotes

  • 4 Corresponding author.

  • E-MAIL shirleen.roeder{at}yale.edu; FAX (203) 432-3263.

    • Received March 30, 1998.
    • Accepted June 12, 1998.
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