Fibrillarin regulates epithelial integrity via EZH2-mediated modulation of scribble expression

Fibrillarin (FBL) is a nucleolar protein critical for rRNA biogenesis. We show that FBL is essential for the maintenance of epithelial integrity through its regulation of cell-cell adhesion proteins. RNA-seq analyses upon FBL depletion revealed deregulation of adhesion- and apical membrane organization-associated pathways. FBL loss deregulates cell polarity via increased deposition of H3K27me3 on the SCRIB promoter, driven by the localization of a subpopulation of EZH2 from the nucleolus to the nucleoplasm. Disrupting the FBL-EZH2 interaction increases cell migration, underscoring a requirement for retaining EZH2 also in the nucleolus. Furthermore, FBL depletion induces EMT in breast epithelial cells, owing to increased levels of mesenchymal factors (Snail1, Twist1, and Zeb1) and activation of Akt. Since Scribble tethers PHLPP1 and PTEN to antagonize Akt, repression of Scribble induces EMT. In summary, FBL safeguards epithelial integrity, by regulating the expression of Scribble, uncovering an FBL-EZH2 axis in EMT and metastasis.

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Publication Details

Journal
Cell Reports
Published
2025-11-25
DOI
https://doi.org/10.1016/j.celrep.2025.116608
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
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article

Fibrillarin regulates epithelial integrity via EZH2-mediated modulation of scribble expression

Sweety Meel, Kundan Sengupta, Santam Saha, Dimple Notani et al.
Cell Reports
RNA Research and Splicing
article

Fibrillarin regulates epithelial integrity via EZH2-mediated modulation of scribble expression

Sweety Meel, Kundan Sengupta, Santam Saha, Dimple Notani, Ashvitha Balaji
article en

Abstract

Fibrillarin (FBL) is a nucleolar protein critical for rRNA biogenesis. We show that FBL is essential for the maintenance of epithelial integrity through its regulation of cell-cell adhesion proteins. RNA-seq analyses upon FBL depletion revealed deregulation of adhesion- and apical membrane organization-associated pathways. FBL loss deregulates cell polarity via increased deposition of H3K27me3 on the SCRIB promoter, driven by the localization of a subpopulation of EZH2 from the nucleolus to the nucleoplasm. Disrupting the FBL-EZH2 interaction increases cell migration, underscoring a requirement for retaining EZH2 also in the nucleolus. Furthermore, FBL depletion induces EMT in breast epithelial cells, owing to increased levels of mesenchymal factors (Snail1, Twist1, and Zeb1) and activation of Akt. Since Scribble tethers PHLPP1 and PTEN to antagonize Akt, repression of Scribble induces EMT. In summary, FBL safeguards epithelial integrity, by regulating the expression of Scribble, uncovering an FBL-EZH2 axis in EMT and metastasis.

Cell ReportsVol. 44(12)
Indian Institute of Science Education and Research Pune (IN), National Centre for Biological Sciences (IN)
Openalex Percentile: Top 67%
RNA Research and Splicing
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