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Journal ArticleDOI

Visualization of the dynamic instability of individual microtubules by dark-field microscopy

Tetsuya Horio, +1 more
- 01 Jun 1986 - 
- Vol. 321, Iss: 6070, pp 605-607
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TLDR
Real-time video recording reveals that both ends of a microtubule exist in either the growing or the shortening phase and alternate quite frequently between the two phases in a stochastic manner, demonstrating directly that growing and shortening populations coexist in steady-state conditions.
Abstract
It has previously been shown that two populations of microtubules coexist in a dynamically unstable manner in vitro: those in one population elongate while those in the other shorten and finally disappear. This conclusion was based on changes in the number and length distribution of microtubules after dilution of the microtubule solution. Here, we demonstrate directly that growing and shortening populations coexist in steady-state conditions, by visualization of the dynamic behaviour of individual microtubules in vitro by dark-field microscopy. Real-time video recording reveals that both ends of a microtubule exist in either the growing or the shortening phase and alternate quite frequently between the two phases in a stochastic manner. Moreover, growing and shortening ends can coexist on a single microtubule, one end continuing to grow simultaneously with shortening at the other end. We find no correlation in the phase conversion either among individual microtubules or between the two ends of a single microtubule. The two ends of any given microtubule have remarkably different characteristics; the active end grows faster, alternates in phase more frequently and fluctuates in length to a greater extent than the inactive end. Microtubule-associated proteins (MAPs) suppress the phase conversion and stabilize microtubules in the growing phase.

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Citations
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Journal ArticleDOI

Microtubule polymerization dynamics

TL;DR: This review describes progress toward understanding the mechanism of dynamic instability of pure tubulin and discusses the function and regulation of microtubule dynamic instability in living cells.
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Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

TL;DR: Antisera raised against synthetic peptides corresponding to these different human tau isoforms demonstrate that multiple tau protein isoforms are incorporated into the neurofibrillary tangles of Alzheimer's disease.
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Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain.

TL;DR: Tau protein is found in the protease‐resistant core of the paired helical filament, the major constituent of the neurofibrillary tangle in Alzheimer's disease.
Journal ArticleDOI

Dynamic Instability of Individual Microtubules Analyzed by Video Light Microscopy: Rate Constants and Transition Frequencies

TL;DR: The data demonstrate that microtubules assembled from pure tubulin undergo dynamic instability over a twofold range of tubulin concentrations, and that the dynamic instability of the plus and minus ends of microtubule can be significantly different.
Book

Mechanics of the cell

TL;DR: The cell is studied as a model for three-dimensional networks, and the role of Membrane undulations in these networks is examined.
References
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Journal ArticleDOI

Dynamic instability of microtubule growth

TL;DR: It is reported here that microtubules in vitro coexist in growing and shrinking populations which interconvert rather infrequently and this dynamic instability is a general property of micro Tubules and may be fundamental in explaining cellular microtubule organization.
Journal ArticleDOI

Microtubule assembly nucleated by isolated centrosomes

TL;DR: It is reported here that purified centrosomes nucleate the assembly of microtubules with unusual dynamic properties, which may have important implications for the mechanism by which microtubule arrays are organized and stabilized in cells.
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Cell motility by labile association of molecules. The nature of mitotic spindle fibers and their role in chromosome movement.

TL;DR: This article summarizes the current views on the dynamic structure of the mitotic spindle and its relation to mitotic chromosome movements based on measurements of birefringence of spindle fibers in living cells, normally developing or experimentally modified by various physical and chemical agents.
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Cyclic AMP-dependent endogenous phosphorylation of a microtubule-associated protein.

TL;DR: The data raise the possibility that the cyclic AMP-dependent phosphorylation of microtubule-associated protein 2 may play a role in microtubules assembly or function.
Journal ArticleDOI

Spindle microtubule dynamics in sea urchin embryos: analysis using a fluorescein-labeled tubulin and measurements of fluorescence redistribution after laser photobleaching.

TL;DR: The rate of exchange of tubulin that is incorporated into spindle microtubules with dimeric tubulin in the cytoplasm has been measured in sea urchin eggs by studying fluorescence redistribution after photobleaching (FRAP), and Dichlorotriazinyl amino fluorescein (DTAF) has been used to label bovine brain tubulin.
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