Comment on "A Centrosome-Independent Role for γ-TuRC Proteins in the Spindle Assembly Checkpoint"-Reference-Cited by-同舟云学术

Comment on "A Centrosome-Independent Role for γ-TuRC Proteins in the Spindle Assembly Checkpoint"

Published:2007-05-18 Issue:5827 Volume:316 Page:982-982
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Weaver Beth A. A.¹,Cleveland Don W.¹

Affiliation:

1. Ludwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093–0670, USA.

Abstract

Müller et al . (Reports, 27 October 2006, p. 654) proposed a role for microtubule nucleation in mitotic checkpoint signaling. However, their observations of spindle defects and mitotic delay after depletion of γ-tubulin ring complex (γ-TuRC) components are fully consistent with activation of the established pathway of checkpoint signaling in response to incomplete or unstable interactions between kinetochores of mitotic chromosomes and spindle microtubules.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference10 articles.

1. The spindle checkpoint: structural insights into dynamic signalling

2. The spindle checkpoint: a quality control mechanism which ensures accurate chromosome segregation

3. Centromeres and Kinetochores

4. A Centrosome-Independent Role for γ-TuRC Proteins in the Spindle Assembly Checkpoint

5. GCP-WD is a γ-tubulin targeting factor required for centrosomal and chromatin-mediated microtubule nucleation

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