mus304 encodes a novel DNA damage checkpoint protein required during Drosophila development

  1. Michael H. Brodsky1,4,
  2. Jeff J. Sekelsky2,3,
  3. Garson Tsang1,
  4. R. Scott Hawley2, and
  5. Gerald M. Rubin1
  1. 1Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley, California 94720 USA; 2Section of Molecular and Cellular Biology, University of California, Davis, California 95616 USA

Abstract

Checkpoints block cell cycle progression in eukaryotic cells exposed to DNA damaging agents. We show that several Drosophilahomologs of checkpoint genes, mei-41, grapes, and14-3-3ε, regulate a DNA damage checkpoint in the developing eye. We have used this assay to show that the mutagen-sensitive gene mus304 is also required for this checkpoint. mus304 encodes a novel coiled-coil domain protein, which is targeted to the cytoplasm. Similar to mei-41,mus304 is required for chromosome break repair and for genomic stability. mus304 animals also exhibit three developmental defects, abnormal bristle morphology, decreased meiotic recombination, and arrested embryonic development. We suggest that these phenotypes reflect distinct developmental consequences of a single underlying checkpoint defect. Similar mechanisms may account for the puzzling array of symptoms observed in humans with mutations in the ATM tumor suppressor gene.

Keywords

Footnotes

  • 3 Present address: Department of Biology, University of North Carolina, Chapel Hill, North Carolina 27599-3280 USA.

  • 4 Corresponding author.

  • E-MAIL brodsky{at}uclink4.berkeley.edu; FAX (510) 643-9947.

    • Received December 2, 1999.
    • Accepted January 31, 2000.
« Previous | Next Article »Table of Contents