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Updated: Jul 14, 2026

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes
Published on: December 20, 2014
Mechanism limiting centrosome duplication to once per cell cycle
Meng-Fu Bryan Tsou1, Tim Stearns
1Department of Biological Sciences, Stanford University, Stanford University Medical School, Stanford, California 94305-5020, USA.
Centrosome duplication is controlled by centriole disengagement, which requires the protease separase during anaphase. This process licenses new centriole growth in the subsequent cell cycle, preventing re-duplication.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- The centrosome, composed of centrioles and pericentriolar material, organizes the microtubule cytoskeleton.
- Cell cycle progression involves a single round of centrosome duplication, ensuring one centrosome per cell before mitosis.
- Newly formed centrioles remain engaged with existing ones until late mitosis or early G1, but the mechanism and timing of this disengagement remain unclear.
Purpose of the Study:
- To elucidate the mechanisms controlling centriole engagement and disengagement.
- To understand the relationship between centriole engagement/disengagement and the potential for centriole duplication.
- To identify the molecular players involved in licensing centriole duplication.
Main Methods:
- Development of an in vitro system using Xenopus egg extract and purified centrioles.
- Analysis of centriole disengagement and growth dynamics.
- Investigation of the roles of separase, anaphase-promoting complex, and Cdk2/cyclin E.
Main Results:
- Centriole disengagement at anaphase is dependent on the anaphase-promoting complex and the protease separase.
- New centriole growth occurs during interphase and requires previously disengaged centrioles and Cdk2/cyclin E activity.
- Centriole engagement prevents re-duplication within the same cell cycle.
Conclusions:
- Centriole disengagement by separase at anaphase licenses centriole duplication for the next cell cycle.
- The cell cycle control of centrosome duplication relies on temporally separating licensing (anaphase) from growth (S phase).
- Separase's role in both centriole disengagement and sister chromatid separation prevents premature disengagement and maintains genomic stability.
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