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Cell division orientation is coupled to cell–cell adhesion by the E-cadherin/LGN complex

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  • Martijn Gloerich

    (Stanford University
    Present address: Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, 3584CG Utrecht, The Netherlands)

  • Julie M. Bianchini

    (Stanford University)

  • Kathleen A. Siemers

    (Stanford University)

  • Daniel J. Cohen

    (Stanford University)

  • W. James Nelson

    (Stanford University
    Stanford University)

Abstract

Both cell–cell adhesion and oriented cell division play prominent roles in establishing tissue architecture, but it is unclear how they might be coordinated. Here, we demonstrate that the cell–cell adhesion protein E-cadherin functions as an instructive cue for cell division orientation. This is mediated by the evolutionarily conserved LGN/NuMA complex, which regulates cortical attachments of astral spindle microtubules. We show that LGN, which adopts a three-dimensional structure similar to cadherin-bound catenins, binds directly to the E-cadherin cytosolic tail and thereby localizes at cell–cell adhesions. On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cadherin to locally form the LGN/NuMA complex. This mediates the stabilization of cortical associations of astral microtubules at cell–cell adhesions to orient the mitotic spindle. Our results show how E-cadherin instructs the assembly of the LGN/NuMA complex at cell–cell contacts, and define a mechanism that couples cell division orientation to intercellular adhesion.

Suggested Citation

  • Martijn Gloerich & Julie M. Bianchini & Kathleen A. Siemers & Daniel J. Cohen & W. James Nelson, 2017. "Cell division orientation is coupled to cell–cell adhesion by the E-cadherin/LGN complex," Nature Communications, Nature, vol. 8(1), pages 1-11, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms13996
    DOI: 10.1038/ncomms13996
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