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10.1038/ncomms8290

http://scihub22266oqcxt.onion/10.1038/ncomms8290
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C4557309!4557309 !26088160
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suck abstract from ncbi

pmid26088160
      Nat+Commun 2015 ; 6 (?): 7290
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  • Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle #MMPMID26088160
  • Lee KY ; Esmaeili B ; Zealley B ; Mishima M
  • Nat Commun 2015[Jun]; 6 (?): 7290 PMID26088160 show ga
  • 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.
  • |Amino Acid Sequence [MESH]
  • |Animals [MESH]
  • |Caenorhabditis elegans [MESH]
  • |Caenorhabditis elegans Proteins/genetics/*metabolism [MESH]
  • |Cytokinesis [MESH]
  • |Kinesins/*metabolism [MESH]
  • |Microtubule-Associated Proteins/*metabolism [MESH]
  • |Molecular Sequence Data [MESH]
  • |Spindle Apparatus/*physiology [MESH]


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