Multivalent afadin interaction promotes IDR-mediated condensate formation and junctional separation of epithelial cells

In epithelial cells, cell-cell adhesion is mediated by the apical junctional complex (AJC), which consists of tight junctions (TJs) and adherens junctions (AJs) aligned from the apical to the basal axis. However, the mechanism of AJC formation on the apical side and the separation of these junctions within AJCs are poorly understood. We find that multivalent interactions of afadin with adhesion molecules and the cytoskeleton lead to condensate formation in an intrinsically disordered region (IDR)-dependent manner, which promotes efficient accumulation in the linear AJ during initial junction formation. Furthermore, we observe that afadin and ZO-1 induce different condensate formations in the cell and that these molecules are differentially distributed from each other. These properties of afadin explain how it strictly localizes to AJs in epithelial cells and is involved in regulating the segregation of AJs and TJs within the AJC.

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Publication Details

Journal
Cell Reports
Published
2025-02-26
DOI
https://doi.org/10.1016/j.celrep.2025.115335
Citations
4
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
3.22
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article

Multivalent afadin interaction promotes IDR-mediated condensate formation and junctional separation of epithelial cells

Shuhei Kuno, Tetsuhisa Otani, Hideru Togashi, Ryu Nakamura
4 citations
Cell Reports
RNA Research and Splicing
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article

Multivalent afadin interaction promotes IDR-mediated condensate formation and junctional separation of epithelial cells

Shuhei Kuno, Tetsuhisa Otani, Hideru Togashi, Ryu Nakamura
article en
4 citations

Abstract

In epithelial cells, cell-cell adhesion is mediated by the apical junctional complex (AJC), which consists of tight junctions (TJs) and adherens junctions (AJs) aligned from the apical to the basal axis. However, the mechanism of AJC formation on the apical side and the separation of these junctions within AJCs are poorly understood. We find that multivalent interactions of afadin with adhesion molecules and the cytoskeleton lead to condensate formation in an intrinsically disordered region (IDR)-dependent manner, which promotes efficient accumulation in the linear AJ during initial junction formation. Furthermore, we observe that afadin and ZO-1 induce different condensate formations in the cell and that these molecules are differentially distributed from each other. These properties of afadin explain how it strictly localizes to AJs in epithelial cells and is involved in regulating the segregation of AJs and TJs within the AJC.

Cell ReportsVol. 44(3)
Japan Science and Technology Agency (JP), Nikon (Japan) (JP), Kobe University (JP), Tokyo Metropolitan University (JP)
Openalex Percentile: Top 9%
RNA Research and Splicing
3.22
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