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Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle.


ABSTRACT: During animal cell division, the central spindle, an anti-parallel microtubule bundle structure formed between segregating chromosomes during anaphase, cooperates with astral microtubules to position the cleavage furrow. Because the central spindle is the only structure linking the two halves of the mitotic spindle, it is under mechanical tension from dynein-generated cortical pulling forces, which determine spindle positioning and drive chromosome segregation through spindle elongation. The central spindle should be flexible enough for efficient chromosome segregation while maintaining its structural integrity for reliable cytokinesis. How the cell balances these potentially conflicting requirements is poorly understood. Here, we demonstrate that the central spindle in C. elegans embryos has a resilient mechanism for recovery from perturbations by excess tension derived from cortical pulling forces. This mechanism involves the direct interaction of two different types of conserved microtubule bundlers that are crucial for central spindle formation, PRC1 and centralspindlin.

SUBMITTER: Lee KY 

PROVIDER: S-EPMC4557309 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle.

Lee Kian-Yong KY   Esmaeili Behrooz B   Zealley Ben B   Mishima Masanori M  

Nature communications 20150619


During animal cell division, the central spindle, an anti-parallel microtubule bundle structure formed between segregating chromosomes during anaphase, cooperates with astral microtubules to position the cleavage furrow. Because the central spindle is the only structure linking the two halves of the mitotic spindle, it is under mechanical tension from dynein-generated cortical pulling forces, which determine spindle positioning and drive chromosome segregation through spindle elongation. The cen  ...[more]

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