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Microtubule Formation01:23

Microtubule Formation

7.8K
Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation...
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Spindle Assembly02:50

Spindle Assembly

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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...
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Microtubule Instability02:17

Microtubule Instability

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Microtubules are hollow cylindrical filaments having a diameter of approximately 25 nm and a length that varies from 200 nm to 25 μm. GTP-bound tubulin subunits form αβ-heterodimers for microtubule assembly. These core building blocks interact longitudinally, polymerizing into protofilaments. The protofilaments then interact with one another through lateral bonding forces to form stable cylindrical microtubules. These cylindrical filaments are dynamic as they undergo repeated...
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Microtubules01:18

Microtubules

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Microtubules are the thickest cytoskeletal filaments with a diameter of 25 nm. In prokaryotic organisms, microtubules are commonly found in locomotory appendages like cilia and flagella. In eukaryotic cells, microtubules form specialized extensions for moving fluid over the surface, like those found in cells lining the intestine.
Microtubules have two structurally similar globular protein subunits: α and β tubulins. In the cytosol, the α and β tubulins form a heterodimer....
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Microtubules01:35

Microtubules

101.8K
There are three types of cytoskeletal structures in eukaryotic cells—microfilaments, intermediate filaments, and microtubules. With a diameter of about 25 nm, microtubules are the thickest of these fibers. Microtubules carry out a variety of functions that include cell structure and support, transport of organelles, cell motility (movement), and the separation of chromosomes during cell division.
101.8K
Anaphase A and B01:39

Anaphase A and B

5.6K
Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
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Related Experiment Video

Updated: Feb 24, 2026

Forming, Confining, and Observing Microtubule-Based Active Nematics
08:37

Forming, Confining, and Observing Microtubule-Based Active Nematics

Published on: January 13, 2023

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Microtubule nucleation: beyond the template.

Johanna Roostalu1, Thomas Surrey1

  • 1The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.

Nature Reviews. Molecular Cell Biology
|August 24, 2017
PubMed
Summary
This summary is machine-generated.

Microtubule nucleation, essential for cell function, is regulated by more than just the gamma-tubulin ring complex. Stabilization of the initial microtubule structure also plays a key role.

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Area of Science:

  • Cell Biology
  • Cytoskeleton Dynamics
  • Molecular Mechanisms

Background:

  • Microtubules are crucial cytoskeletal components in eukaryotic cells, involved in vital cellular processes.
  • While microtubule dynamics are well-understood, the mechanisms of microtubule nucleation remain largely unclear.
  • The gamma-tubulin ring complex is the primary known nucleation template.

Purpose of the Study:

  • To investigate the molecular mechanisms underlying microtubule nucleation.
  • To explore the role of microtubule-associated proteins in nucleation.
  • To propose a conceptual framework for microtubule nucleation regulation.

Main Methods:

  • Review of existing literature on microtubule nucleation and associated proteins.
  • Analysis of experimental data on microtubule dynamics and nucleation.
  • Conceptual modeling of nucleation processes.

Main Results:

  • Microtubule nucleation is influenced by factors beyond the gamma-tubulin ring complex.
  • Microtubule-associated proteins contribute to the nucleation process.
  • Stabilization of the nascent microtubule nucleus is a critical regulatory step.

Conclusions:

  • Microtubule nucleation efficiency is controlled by both template activity and the stabilization of the growing microtubule.
  • A unified conceptual framework integrating template and stabilization mechanisms is proposed.
  • Further research is needed to fully elucidate the complex regulation of microtubule nucleation.