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18.7:

Microtubule Instability

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Biologia Molecular
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JoVE Core Biologia Molecular
Microtubule Instability

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In eukaryotic cells, during cell division, microtubules form the main components of the mitotic spindle and are required for chromosome segregation.

Microtubules are extremely dynamic. Individual microtubules grow, shrink, and rapidly alternate between the growing and shortening phases. Microtubules exhibit dynamic instability, the unpredictable change between growth and shrinkage.

The shift from growth to shrinkage is called a catastrophe and the shift from shrinkage to growth is called a rescue. At any point in time, a group of microtubules is actively assembling, while others are rapidly disassembling.

Microtubules nucleate and grow by the end-to-end polymerization of GTP-bound tubulin heterodimers. The tubulin heterodimer comprises an alpha and beta subunit.

The beta-tubulin subunit is bound to a hydrolyzable form of GTP. The hydrolysis of GTP to GDP destabilizes the microtubule framework. The structure splays out at the tip and the effect propagates down, causing depolymerization of the microtubule.

A variety of regulatory proteins control microtubule dynamics. Several microtubule-associated proteins or MAPs promote microtubule stability, while several other proteins, the catastrophe factors, destabilize the microtubules. Cells alter the activity of regulatory proteins to change microtubule dynamics dependent upon the phase of the cell cycle.

For example, during interphase, most animal cells contain a cytoplasmic array of long microtubules radiating from a single centrosome. As cells transition to the mitotic phase and duplicated centrosomes move towards the opposite poles, microtubule instability increases.

Microtubule instability facilitates the formation of a dense, dynamic array of mitotic microtubules, contributing to the spindle formation.

18.7:

Microtubule Instability

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 assembly and disassembly. This characteristic dynamic instability can be found both in vivo and in vitro.

Dynamic Instability

Individual microtubules may elongate and shrink simultaneously on the opposite ends at a given point in time. Whether a microtubule is growing or shrinking is determined by its rates of catastrophe and rescue. Catastrophe is when a growing microtubule begins to shorten rapidly. Rescue is the shift of a shrinking microtubule to elongate rapidly. The rate of β-tubulin bound-GTP hydrolysis is a primary factor that determines the dynamic instability.

In the cell, both free tubulin subunits and their αβ-heterodimeric forms are present in the cytoplasmic pool. The polymerization of tubulin subunits initiates when GTP-bound αβ-heterodimeric subunits are above a threshold concentration, referred to as the critical concentration for microtubule polymerization. β-tubulin exists in two forms. The GTP-bound-β-tubulin or T-form is responsible for the elongation and stable linear structure of microtubules. In contrast, the GDP-bound-β-tubulin or D-form favors microtubule disassembly.   The GTP-bound-β-tubulins at the growing end act as a cap, preventing protofilament curvature and promoting elongation. Upon hydrolysis of GTP, the conformation of β-tubulin is slightly altered, resulting in protofilament curving. This curving facilitates the binding of destabilizing proteins like stathmin and kinesin-13 to remove the αβ-tubulin heterodimers.

Factors regulating the instability

Microtubule-associated proteins or the MAPs are critical regulators of microtubule dynamic instability. MAPs are broadly classified as stabilizers and destabilizers based on their function in microtubule dynamics. The stabilizer MAPs bind with the microtubules to reduce the catastrophe event and to promote elongation. On the other hand, the destabilizers bind to promote the catastrophe. Stabilizer MAPs are dominant during the interphase and in axonal and dendritic microtubules of neurons, promoting stable assemblies. During mitosis, destabilizer MAPs are more common. These MAPs are responsible for the chromosome segregation and the disassembly of the cytoskeletal mesh for cell division.

Leitura Sugerida

  1. de Forges, H., Bouissou, A. and Perez, F., 2012. Interplay between microtubule dynamics and intracellular organization. The international journal of biochemistry & cell biology, 44(2), pp.266-274. https://doi.org/10.1016/j.biocel.2011.11.009
  2. Burbank, K.S. and Mitchison, T.J., 2006. Microtubule dynamic instability. Current Biology, 14(16), pp.R516-R517. https://doi.org/10.1016/j.cub.2006.06.044
  3. Vaart, B.V.D., Akhmanova, A. and Straube, A., 2009. Regulation of microtubule dynamic instability. Biochemical Society Transactions, 37(5), pp.1007-1013. https://doi.org/10.1042/BST0371007