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Spindle Assembly02:50

Spindle Assembly

Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a microtubule array...
Centrioles and Centrosomes01:13

Centrioles and Centrosomes

Most animal cells comprise a pair of centrioles together called a centrosome. The cell duplicates its centrosome and contains two centrosomes side-by-side, which begin to move apart during the prophase. As the centrosomes migrate to two different sides of the cell, microtubules start extending from each centrosome toward the other end. The mitotic spindle is composed of the centrosomes and their emerging microtubules.
Near the end of the prophase, also called late prophase or "prometaphase,"...
Centrosome Duplication02:25

Centrosome Duplication

The primary microtubule organizing center (MTOC) in animal cells is the centrosome. A centrosome has two cylindrical centrioles at its core. Each centriole consists of nine sets of three microtubules held together by proteins. The centrioles are positioned at right angles to each other and surrounded by a shapeless protein cloud called the pericentriolar matrix, or pericentriolar material (PCM).
To ensure that each daughter cell receives a centrosome after cell division, centrosome duplication...
Centrosome Duplication02:25

Centrosome Duplication

The primary microtubule organizing center (MTOC) in animal cells is the centrosome. A centrosome has two cylindrical centrioles at its core. Each centriole consists of nine sets of three microtubules held together by proteins. The centrioles are positioned at right angles to each other and surrounded by a shapeless protein cloud called the pericentriolar matrix, or pericentriolar material (PCM).
To ensure that each daughter cell receives a centrosome after cell division, centrosome duplication...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.

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Related Experiment Video

Updated: Jun 13, 2026

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes
09:39

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes

Published on: December 20, 2014

Stepwise evolution of the centriole-assembly pathway.

Zita Carvalho-Santos1, Pedro Machado, Pedro Branco

  • 1Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6, P-2780-156 Oeiras, Portugal.

Journal of Cell Science
|April 16, 2010
PubMed
Summary

A conserved ancestral module (UNIMOD) of centriole and basal body (CBB) assembly explains conserved CBB structure. Taxon-specific innovations drive CBB diversity and function in eukaryotes.

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Last Updated: Jun 13, 2026

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes
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Area of Science:

  • Cell Biology
  • Evolutionary Biology
  • Biochemistry

Background:

  • Centriole and basal body (CBB) structures are crucial for cilia, flagella, and centrosomes, underpinning cell motility, division, and polarity.
  • While CBB assembly components are known, their regulation and evolutionary history remain largely unexplored.
  • Understanding CBB assembly mechanisms is key, given the diversity of eukaryotic cellular contexts and the conserved CBB morphology.

Purpose of the Study:

  • To investigate general mechanistic principles governing CBB assembly across eukaryotes.
  • To analyze the distribution of human CBB-assembly machinery components across eukaryotes to generate hypotheses.
  • To elucidate the evolutionary origins and diversification of CBB assembly factors.

Main Methods:

  • Comparative analysis of CBB-assembly machinery component distribution across eukaryotic taxa.
  • Identification of evolutionarily conserved modules and taxon-specific components.
  • Experimental investigation of gene duplication, protein divergence, and cross-species complementation.

Main Results:

  • An evolutionarily cohesive, ancestral module (UNIMOD), comprising SAS6, SAS4/CPAP, and BLD10/CEP135, correlates with CBB occurrence.
  • Other components like SAK/PLK4, SPD2/CEP192, and CP110 emerged in a taxon-specific manner.
  • Gene duplication significantly impacts CBB component evolution, leading to tissue specificity (e.g., BLD10/CEP135) and species-specific adaptations (e.g., SAK/PLK4 divergence).

Conclusions:

  • The UNIMOD theory provides a framework for understanding the conserved architecture of CBBs.
  • Taxon- and tissue-specific innovations, arising from gene emergence, duplication, and divergence, are critical for coordinating CBB biogenesis and function.
  • Species-specific adaptations in CBB assembly components contribute to functional diversity in different cellular contexts.