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A meiotic recombination checkpoint controlled by mitotic checkpoint genes

Abstract

IN budding yeast, meiotic recombination occurs at about 200 sites per cell and involves DNA double-strand break (DSB) intermediates1–3. Here we provide evidence that a checkpoint control requiring the mitotic DNA-damage checkpoint genes RAD17, RAD24 and MEC1 ensures that meiotic recombination is complete before the first meiotic division (MI). First, RAD17, RAD24 and MEC1 are required for the meiotic arrest caused by blocking the repair of DSBs with a mutation in the recA homologue DMC1. Second, mec1 and rad24 single mutants (DMC1+) appear to undergo MI before all recombination events are complete. Curiously, the mitosis-specific checkpoint gene RAD9 is not required for meiotic arrest of dmc1 mutants4. This shows that although mitotic and meiotic control mechanisms are related, they differ significantly. Rad17 and Rad24 proteins may contribute directly to formation of an arrest signal by association with single-strand DNA in mitosis and meiosis.

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References

  1. Sun, H., Treco, D., Schultes, N. P. & Szostak, J. W. Nature 338, 87–90 (1989).

    Article  ADS  CAS  Google Scholar 

  2. Cao, L., Alani, E. & Kleckner, N. Cell 61, 1089–1101 (1990).

    Article  CAS  Google Scholar 

  3. Wu, T.-C. & Lichten, M. Science 263, 515–518 (1994).

    Article  ADS  CAS  Google Scholar 

  4. Bishop, D. K., Park, D., Xu, L. & Kleckner, N. Cell 69, 439–456 (1992).

    Article  CAS  Google Scholar 

  5. Sandell, L. L. & Zakian, V. A. Cell 75, 729–739 (1993).

    Article  CAS  Google Scholar 

  6. Hartwell, L. H. & Weinert, T. A. Science 246, 629–634 (1989).

    Article  ADS  CAS  Google Scholar 

  7. Lydall, D. & Weinert, T. Curr. Opin. Gen. Dev. 6, 4–11 (1996).

    Article  CAS  Google Scholar 

  8. Lydall, D. & Weinert, T. Science 270, 1488–1491 (1995).

    Article  ADS  CAS  Google Scholar 

  9. Weinert, T. A., Kiser, G. L. & Hartwell, L. H. Genes Dev. 8, 652–665 (1994).

    Article  CAS  Google Scholar 

  10. Sanchez, Y. et al. Science 271, 357–360 (1996).

    Article  ADS  CAS  Google Scholar 

  11. Sun, Z., Fay, D. S., Marini, F., Foiani, M. & Stern, D. F. Genes Dev. 10, 395–406 (1996).

    Article  CAS  Google Scholar 

  12. Sym, M., Engebreacht, J. & Roeder, G. S. Cell 72, 365–378 (1993).

    Article  CAS  Google Scholar 

  13. Sym, M. & Roeder, G. S. Cell 79, 283–292 (1994).

    Article  CAS  Google Scholar 

  14. Game, J. C., Jamb, T. J., Braun, R. J., Resnick, M. & Roth, R. M. Genetics 94, 51–68 (1980).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Malone, R. E. & Esposito, R. E. Mol. Cell. Biol. 1, 891–901 (1981).

    Article  CAS  Google Scholar 

  16. Klapholz, S., Waddell, C. S. & Esposito, R. E. Genetics 110, 187–216 (1985).

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Alani, E., Padmore, R. & Kleckner, N. Cell 61, 419–436 (1990).

    Article  CAS  Google Scholar 

  18. Schwacha, A. & Kleckner, N. Cell 76, 51–63 (1994).

    Article  CAS  Google Scholar 

  19. Xu, L. & Kleckner, N. Genes Dev. (in the press).

  20. Shinohara, A., Ogawa, H. & Ogawa, T. Cell 69, 457–470 (1992).

    Article  CAS  Google Scholar 

  21. Bishop, D. K. Cell 79, 1081–1092 (1994).

    Article  CAS  Google Scholar 

  22. Hari, L. K. et al. Cell 82, 815–821 (1995).

    Article  CAS  Google Scholar 

  23. Baker, B. & Carpenter, A. T. C. Genetics 71, 255–286 (1972).

    CAS  PubMed  PubMed Central  Google Scholar 

  24. Kato, R. & Ogawa, H. Nucleic Acids Res 22, 3104–3112 (1994).

    Article  CAS  Google Scholar 

  25. Ogawa, T. et al. Cold Spring Harb. Symp. Quant. Biol. 58, 567–576 (1993).

    Article  CAS  Google Scholar 

  26. Garvik, B., Carson, M. & Hartwell, L. Mol. Cell. Biol. 15, 6128–6138 (1995).

    Article  CAS  Google Scholar 

  27. White, C. I. & Haber, J. E. EMBO J. 9, 663–673 (1990).

    Article  CAS  Google Scholar 

  28. Weber, L. & Byers, B. Genetics 131, 55–63 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Weinert, T. A. & Lydall, D. in DNA Damage and Repair (eds Nickoloff, J. A. & Hoekstra, M.) (Humana in the press).

  30. Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Laboratory Press, NY, 1989).

    Google Scholar 

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Lydall, D., Nikolsky, Y., Bishop, D. et al. A meiotic recombination checkpoint controlled by mitotic checkpoint genes. Nature 383, 840–843 (1996). https://doi.org/10.1038/383840a0

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