N-terminal nesprin-2 variants regulate β-catenin signalling

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)
186 Downloads (Pure)

Abstract

The spatial compartmentalisation of biochemical signalling pathways is essential for cell function. Nesprins are a multi-isomeric family of proteins that have emerged as signalling scaffolds, herein, we investigate the localisation and function of novel nesprin-2 N-terminal variants. We show that these nesprin-2 variants display cell specific distribution and reside in both the cytoplasm and nucleus. Immunofluorescence microscopy revealed that nesprin-2 N-terminal variants colocalised with β-catenin at cell-cell junctions in U2OS cells. Calcium switch assays demonstrated that nesprin-2 and β-catenin are lost from cell-cell junctions in low calcium conditions whereas emerin localisation at the NE remained unaltered, furthermore, an N-terminal fragment of nesprin-2 was sufficient for cell-cell junction localisation and interacted with β-catenin. Disruption of these N-terminal nesprin-2 variants, using siRNA depletion resulted in loss of β-catenin from cell-cell junctions, nuclear accumulation of active β-catenin and augmented β-catenin transcriptional activity. Importantly, we show that U2OS cells lack nesprin-2 giant, suggesting that the N-terminal nesprin-2 variants regulate β-catenin signalling independently of the NE. Together, these data identify N-terminal nesprin-2 variants as novel regulators of β-catenin signalling that tether β-catenin to cell-cell contacts to inhibit β-catenin transcriptional activity.
Original languageEnglish
JournalExperimental Cell Research
DOIs
Publication statusPublished - 16 Jun 2016

Keywords

  • Nesprin-2
  • β-catenin
  • Cell-cell junctions
  • Scaffold protein

Fingerprint

Dive into the research topics of 'N-terminal nesprin-2 variants regulate β-catenin signalling'. Together they form a unique fingerprint.

Cite this