Switching from weak to strong cortical attachment of microtubules accounts for the transition from nuclear centration to spindle elongation in metazoans

© 2024 The Authors. Published by Elsevier Ltd..

The centrosome is a major microtubule organizing center in animal cells. The position of the centrosomes inside the cell is important for cell functions such as cell cycle, and thus should be tightly regulated. Theoretical models based on the forces generated along the microtubules have been proposed to account for the dynamic movements of the centrosomes during the cell cycle. These models, however, often adopted inconsistent assumptions to explain distinct but successive movements, thus preventing a unified model for centrosome positioning. For the centration of the centrosomes, weak attachment of the astral microtubules to the cell cortex was assumed. In contrast, for the separation of the centrosomes during spindle elongation, strong attachment was assumed. Here, we mathematically analyzed these processes at steady state and found that the different assumptions are proper for each process. We experimentally validated our conclusion using nematode and sea urchin embryos by manipulating their shapes. Our results suggest the existence of a molecular mechanism that converts the cortical attachment from weak to strong during the transition from centrosome centration to spindle elongation.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:10

Enthalten in:

Heliyon - 10(2024), 3 vom: 15. Feb., Seite e25494

Sprache:

Englisch

Beteiligte Personen:

Tada, Shohei [VerfasserIn]
Yamazaki, Yoshitaka [VerfasserIn]
Yamamoto, Kazunori [VerfasserIn]
Fujii, Ken [VerfasserIn]
Yamada, Takahiro G [VerfasserIn]
Hiroi, Noriko F [VerfasserIn]
Kimura, Akatsuki [VerfasserIn]
Funahashi, Akira [VerfasserIn]

Links:

Volltext

Themen:

Astral microtubules
Cell cycle
Centrosome centration
Journal Article
Mathematical modeling
Spindle elongation

Anmerkungen:

Date Revised 16.02.2024

published: Electronic-eCollection

Citation Status PubMed-not-MEDLINE

doi:

10.1016/j.heliyon.2024.e25494

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM368467147