Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
AAAS Promotion

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 18 May 2007:
Vol. 316. no. 5827, p. 982
DOI: 10.1126/science.1136935

Technical Comments

Response to Comments on "A Centrosome-Independent Role for {gamma}-TuRC Proteins in the Spindle Assembly Checkpoint"

Hannah Müller, Marie-Laure Fogeron, Verena Lehmann, Hans Lehrach, Bodo M. H. Lange*

Weaver and Cleveland and Taylor et al. contend that our data on the involvement of the {gamma}-tubulin ring complex ({gamma}-TuRC) in the spindle assembly checkpoint (SAC) can be fully explained by kinetochore-derived checkpoint signaling. We maintain that (i) the interactions of {gamma}-TuRC with Cdc20 and BubR1, and (ii) the activation of SAC by {gamma}-TuRC depletion, in addition to the abrogation of kinetochore-microtubule interactions, argue for a more complex mechanism of SAC signaling.

Department of Vertebrate Genomics, Max-Planck Institute for Molecular Genetics, Ihnestrasse 73, D-14195 Berlin, Germany.

* To whom correspondence should be addressed. E-mail: lange_b{at}molgen.mpg.de

Read the Full Text






ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)