ArticleThe Journal of cell biology1989
Cell cycle-dependent changes in the dynamics of MAP 2 and MAP 4 in cultured cells.
Article in The Journal of cell biology, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed, 52 citations in OpenAlex.
- Emerging Insights into the Function of Kinesin-8 Proteins in Microtubule Length Regulation.Biomolecules · 2018Review
- Tobacco microtubule-associated protein, MAP65-1c, bundles and stabilizes microtubules.Plant molecular biology · 2010Article
- The C-terminal variable region specifies the dynamic properties of Arabidopsis microtubule-associated protein MAP65 isotypes.The Plant cell · 2008Article
- Swimming against the tide: mobility of the microtubule-associated protein tau in neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007Article
- Mammalian septins regulate microtubule stability through interaction with the microtubule-binding protein MAP4.Molecular biology of the cell · 2005Article
- MARK/PAR1 kinase is a regulator of microtubule-dependent transport in axons.The Journal of cell biology · 2004Article
- EB1-microtubule interactions in Xenopus egg extracts: role of EB1 in microtubule stabilization and mechanisms of targeting to microtubules.Molecular biology of the cell · 2002Article
- Single-molecule investigation of the interference between kinesin, tau and MAP2c.The EMBO journal · 2002Article
- The endogenous and cell cycle-dependent phosphorylation of tau protein in living cells: implications for Alzheimer's disease.Molecular biology of the cell · 1998Article
- XMAP310: a Xenopus rescue-promoting factor localized to the mitotic spindle.The Journal of cell biology · 1997Article
- Domains of neuronal microtubule-associated proteins and flexural rigidity of microtubules.The Journal of cell biology · 1997Article
- Mapmodulin: a possible modulator of the interaction of microtubule-associated proteins with microtubules.Proceedings of the National Academy of Sciences of the United States of America · 1997Article
- Removal of MAP4 from microtubules in vivo produces no observable phenotype at the cellular level.The Journal of cell biology · 1996Article
- Binding of E-MAP-115 to microtubules is regulated by cell cycle-dependent phosphorylation.The Journal of cell biology · 1995Article
- Analysis of MAP 4 function in living cells using green fluorescent protein (GFP) chimeras.The Journal of cell biology · 1995Article
- Cyclin B interaction with microtubule-associated protein 4 (MAP4) targets p34cdc2 kinase to microtubules and is a potential regulator of M-phase microtubule dynamics.The Journal of cell biology · 1995Article
- Dynamics of microtubules bundled by microtubule associated protein 2C (MAP2C).The Journal of cell biology · 1993Article
- Phosphorylation determines the binding of microtubule-associated protein 2 (MAP2) to microtubules in living cells.The Journal of cell biology · 1991Article
- Microtubules are stabilized in confluent epithelial cells but not in fibroblasts.The Journal of cell biology · 1990Article
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
To examine the behavior of microtubule-associated proteins (MAPs) in living cells, MAP 4 and MAP 2 have been derivatized with 6-iodoacetamido-fluorescein, and the distribution of microinjected MAP has been analyzed using a low light level video system and fluorescence redistribution after photobleaching. Within 1 min following microinjection of fluoresceinated MAP 4 or MAP 2, fluorescent microtubule arrays were visible in interphase or mitotic PtK1 cells. After cold treatment of fluorescent MAP 2-containing cells (3 h, 4 degrees C), microtubule fluorescence disappeared, and the only fluorescence above background was located at the centrosomes; microtubule patterns returned upon warming. Loss of microtubule immunofluorescence after nocodozole treatment was similar in MAP-injected and control cells, suggesting that injected fluorescein-labeled MAP 2 did not stabilize microtubules. The dynamics of the MAPs were examined further by FRAP. FRAP analysis of interphase cells demonstrated that MAP 2 redistributed with half-times slightly longer (60 +/- 25 s) than those for MAP 4 (44 +/- 20 s), but both types of MAPs bound to microtubules in vivo exchanged with soluble MAPs at rates exceeding the rate of tubulin turnover. These data imply that microtubules in interphase cells are assembled with constantly exchanging populations of MAP. Metaphase cells at 37 degrees C or 26 degrees C showed similar mean redistribution half-times for both MAP 2 and MAP 4; these were 3-4 fold faster than the interphase rates (MAP 2, t1/2 = 14 +/- 6 s; MAP 4, t1/2 = 17 +/- 5 s). The extent of recovery of spindle fluorescence in MAP-injected cells was to 84-94% at either 26 or 37 degrees C. Although most metaphase tubulin, like the MAPs, turns over rapidly and completely under physiologic conditions, published work shows either reduced rates or extents of turnover at 26 degrees C, suggesting that the fast mitotic MAP exchange is not simply because of fast tubulin turnover. Exchange of MAP 4 bound to telophase midbodies occurred with dynamics comparable to those seen in metaphase spindles (t1/2 = approximately 27 s) whereas midbody tubulin exchange was slow (greater than 300 s). These data demonstrate that the rate of MAP exchange on microtubules is a function of time in the cell cycle.
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