Persistent growth of microtubules at low density.


Journal

Molecular biology of the cell
ISSN: 1939-4586
Titre abrégé: Mol Biol Cell
Pays: United States
ID NLM: 9201390

Informations de publication

Date de publication:
01 03 2021
Historique:
pubmed: 14 1 2021
medline: 17 8 2021
entrez: 13 1 2021
Statut: ppublish

Résumé

Microtubules (MTs) often form a polarized array with minus ends anchored at the centrosome and plus ends extended toward the cell margins. Plus ends display behavior known as dynamic instability-transitions between rapid shortening and slow growth. It is known that dynamic instability is regulated locally to ensure entry of MTs into nascent areas of the cytoplasm, but details of this regulation remain largely unknown. Here, we test an alternative hypothesis for the local regulation of MT behavior. We used microsurgery to isolate a portion of peripheral cytoplasm from MTs growing from the centrosome, creating cytoplasmic areas locally depleted of MTs. We found that in sparsely populated areas MT plus ends persistently grew or paused but never shortened. In contrast, plus ends that entered regions of cytoplasm densely populated with MTs frequently transitioned to shortening. Persistent growth of MTs in sparsely populated areas could not be explained by a local increase in concentration of free tubulin subunits or elevation of Rac1 activity proposed to enhance MT growth at the cell leading edge during locomotion. These observations suggest the existence of a MT density-dependent mechanism regulating MT dynamics that determines dynamic instability of MTs in densely populated areas of the cytoplasm and persistent growth in sparsely populated areas.

Identifiants

pubmed: 33439670
doi: 10.1091/mbc.E20-08-0546
pmc: PMC8098851
doi:

Substances chimiques

Microtubule-Associated Proteins 0
Tubulin 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

435-445

Subventions

Organisme : FDA HHS
ID : R01 FD003937
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM062290
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM117061
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS099730
Pays : United States

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Auteurs

Anton Burakov (A)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.
A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.

Ivan Vorobjev (I)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.
A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.
Department of Biology, School of Sciences and Humanities and National Laboratory Astana, Nazarbayev University, 010000 Nur-Sultan, Kazakhstan.

Irina Semenova (I)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.

Ann Cowan (A)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.

John Carson (J)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.

Yi Wu (Y)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.

Vladimir Rodionov (V)

R.D. Berlin Center for Cell Analysis and Modeling and Department of Cell Biology, UConn Health, Farmington, CT 06030.

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