Mutation of a Drosophila gamma tubulin ring complex subunit encoded by discs degenerate-4 differentially disrupts centrosomal protein localization

  1. Vitor Barbosa,
  2. Rochele R. Yamamoto,
  3. Daryl S. Henderson, and
  4. David M. Glover1
  1. Cancer Research Campaign, Cell Cycle Genetics Group, University of Cambridge, Department of Genetics, Cambridge, UK

Abstract

We have cloned the Drosophila gene discs degenerate-4 (dd4) and find that it encodes a component of the γ-tubulin ring complex (γTuRC) homologous to Spc98 of budding yeast. This provides the first opportunity to study decreased function of a member of the γ-tubulin ring complex, other than γ-tubulin itself, in a metazoan cell. γ-tubulin is no longer at the centrosomes but is dispersed throughout dd4 cells and yet bipolar metaphase spindles do form, although these have a dramatically decreased density of microtubules. Centrosomin (CNN) remains in broad discrete bodies but only at the focused poles of such spindles, whereas Asp (abnormal spindleprotein) is always present at the presumptive minus ends of microtubules, whether or not they are focused. This is consistent with the proposed role of Asp in coordinating the nucleation of mitotic microtubule organizing centers. The centrosome associated protein CP190 is partially lost from the spindle poles in dd4cells supporting a weak interaction with γ-tubulin, and the displaced protein accumulates in the vicinity of chromosomes. Electron microscopy indicates not only that the poles of dd4 cells have irregular amounts of pericentriolar material, but also that they can have abnormal centrioles. In six dd4 cells subjected to serial sectioning centrioles were missing from one of the two poles. This suggests that in addition to its role in nucleating cytoplasmic and spindle microtubules, the γTuRC is also essential to the structure of centrioles and the separation of centrosomes.

Keywords

Footnotes

  • 1 Corresponding author.

  • E-MAIL dmg25{at}mole.bio.cam.ac.uk; FAX 44-1223-333968.

  • Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.182800.

    • Received June 16, 2000.
    • Accepted October 24, 2000.
| Table of Contents

Life Science Alliance