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

Martijn Gloerich*, Julie M. Bianchini, Kathleen A. Siemers, Daniel J. Cohen, W. James Nelson

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
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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.

Original languageEnglish
Article number13996
JournalNature Communications [E]
Volume8
DOIs
Publication statusPublished - 3 Jan 2017

Keywords

  • Animals
  • Antigens, CD
  • Antigens, Nuclear/chemistry
  • Binding Sites
  • Cadherins/chemistry
  • Cell Adhesion
  • Cell Communication
  • Cell Cycle Proteins
  • Cell Division
  • Cell Line
  • Dogs
  • Drosophila melanogaster/cytology
  • Epithelial Cells/metabolism
  • Gene Expression
  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins/chemistry
  • Madin Darby Canine Kidney Cells
  • Microtubules/metabolism
  • Models, Molecular
  • Nuclear Matrix-Associated Proteins/chemistry
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Structure, Secondary
  • Recombinant Proteins/chemistry
  • Spindle Apparatus/metabolism

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