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Open AccessJournal ArticleDOI

The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries

Erich A. Nigg, +1 more
- 01 Oct 2011 - 
- Vol. 13, Iss: 10, pp 1154-1160
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TLDR
The spatial aspects of the centrosome duplication cycle, the mechanism of centriole assembly and the possible consequences of the inherent asymmetry of Centrosomes and centrosomes are discussed.
Abstract
Centrosomes are microtubule-organizing centres of animal cells. They influence the morphology of the microtubule cytoskeleton, function as the base for the primary cilium and serve as a nexus for important signalling pathways. At the core of a typical centrosome are two cylindrical microtubule-based structures termed centrioles, which recruit a matrix of associated pericentriolar material. Cells begin the cell cycle with exactly one centrosome, and the duplication of centrioles is constrained such that it occurs only once per cell cycle and at a specific site in the cell. As a result of this duplication mechanism, the two centrioles differ in age and maturity, and thus have different functions; for example, the older of the two centrioles can initiate the formation of a ciliary axoneme. We discuss spatial aspects of the centrosome duplication cycle, the mechanism of centriole assembly and the possible consequences of the inherent asymmetry of centrioles and centrosomes.

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Journal ArticleDOI

Centrosome function and assembly in animal cells

TL;DR: Advances should ultimately allow the in vitro reconstitution of functional centrosomes from their component proteins to unlock the secrets of these enigmatic organelles.
Journal ArticleDOI

Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization

TL;DR: It is demonstrated that the pericentriolar material is organized into two main structural domains: a layer juxtaposed to the centriole wall, and proteins extending farther away from the Centrosome organized in a matrix, using SIM and STORM subdiffraction-resolution microscopies.
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Targeting Mitosis in Cancer: Emerging Strategies

TL;DR: The concept of exploiting the genomic instability of tumor cells through therapeutic inhibition of mitotic checkpoints is discussed, and it is believed this strategy has a high likelihood of success given its potential to enhance therapeutic index by targeting tumor-specific vulnerabilities.
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Phase transitions and size scaling of membrane-less organelles.

TL;DR: The phase transitions that appear to govern the assembly of membrane-less cytoplasmic and nucleoplasmic structures exhibit an intrinsic dependence on cell size, and may explain the size scaling reported for a number of structures.
Journal ArticleDOI

Once and only once: mechanisms of centriole duplication and their deregulation in disease

TL;DR: A better understanding of the molecular mechanisms governing centriole biogenesis is understood, opening up new possibilities for targeting these pathways in the context of human disease.
References
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Journal ArticleDOI

Asymmetric inheritance of centrosomally localized mRNAs during embryonic cleavages.

TL;DR: A third mechanism of asymmetric inheritance in a mollusc embryo is reported, which produces a complex pattern of mRNA localization, in which different messages distinguish groups of cells with the same birth order rank and similar developmental potentials.
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A genome-wide RNAi screen to dissect centriole duplication and centrosome maturation in Drosophila.

TL;DR: A microscopy-based genome-wide RNA interference screen in Drosophila cells to identify proteins required for centriole duplication and mitotic PCM recruitment finds that the individual depletion of only two proteins, Polo and Centrosomin (Cnn) can completely block centrosome maturation.
Journal ArticleDOI

Control of daughter centriole formation by the pericentriolar material.

TL;DR: Laser microsurgery is used to test the hypothesis that attachment of the daughter centriole to the wall of the mother inhibits formation of additional daughters, and proposes that that the size of the PCM cloud associated with the mother centrioles restricts the number of daughters that can form simultaneously.
Journal ArticleDOI

De novo formation of centrosomes in vertebrate cells arrested during S phase

TL;DR: In this article, the authors show that when centrosomes are completely destroyed by laser microsurgery in CHO cells arrested in S phase by hydroxyurea, new centrosome form by de novo assembly.
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