Abstract

The centrosome serves as a major microtubule-organizing center (MTOC). The Cdc6 protein is a component of the pre-replicative complex and a licensing factor for the initiation of chromosome replication and localizes to centrosomes during the S and G2 phases of the cfell cycle of human cells. This cell cycle-dependent localization of Cdc6 to the centrosome motivated us to investigate whether Cdc6 negatively regulates MTOC activity and to determine the integral proteins that comprise the pericentriolar material (PCM). Time-lapse live-cell imaging of microtubule regrowth revealed that Cdc6 depletion increased microtubule nucleation at the centrosomes and that expression of Cdc6 in Cdc6-depleted cells reversed this effect. This increase and decrease in microtubule nucleation correlated with the centrosomal intensities of PCM proteins such as γ-tubulin, pericentrin, CDK5 regulatory subunit-associated protein 2 (CDK5RAP2), and centrosomal protein 192 (Cep192). The regulation of microtubule nucleation and the recruitment of PCM proteins to the centrosome required Cdc6 ATPase activity, as well as a centrosomal localization of Cdc6. These results suggest a novel function for Cdc6 in coordinating centrosome assembly and function.

Highlights

  • The centrosome serves as a major microtubule-organizing center (MTOC)

  • Because the centrosomal localization of Cdc6 negatively regulates microtubule nucleation, we investigated whether Cdc6 could affect ␥-tubulin levels at the centrosome. ␥-Tubulin of the ␥-TuRC functions as a nucleation core for microtubule polymerization [7,8,9]

  • Cdc6 participates in pre-replicative complex (pre-RC) formation in the nucleus during the G1 phase, its protein levels are lowest during the G1 phase, and its mRNA and protein levels begin to increase from S phase [32,33,34]

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Summary

ARTICLE cro

The DNA replication protein Cdc inhibits the microtubuleorganizing activity of the centrosome. The Cdc protein is a component of the prereplicative complex and a licensing factor for the initiation of chromosome replication and localizes to centrosomes during the S and G2 phases of the cfell cycle of human cells. This cell cycle-dependent localization of Cdc to the centrosome motivated us to investigate whether Cdc negatively regulates MTOC activity and to determine the integral proteins that comprise the pericentriolar material (PCM). The regulation of microtubule nucleation and the recruitment of PCM proteins to the centrosome required Cdc ATPase activity, as well as a centrosomal localization of Cdc6 These results suggest a novel function for Cdc in coordinating centrosome assembly and function.

Results
Discussion
DNA construction and transfection
Cell culture and cell line construction
Microtubule regrowth assay
Immunofluorescence microscopy
Statistical analysis
Full Text
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