Julia Fiedler, Thomas Moennig, Johanna H Hinrichs, Annika Weber, Thomas Wagner, Tim Hemmer, Rita Schröter, Thomas Weide, Daniel Epting, Carsten Bergmann, Pavel Nedvetsky, Michael P Krahn
Cellular and molecular life sciences : CMLS 2023 Oct 25The conserved multiple PDZ-domain containing protein PATJ stabilizes the Crumbs-Pals1 complex to regulate apical-basal polarity and tight junction formation in epithelial cells. However, the molecular mechanism of PATJ's function in these processes is still unclear. In this study, we demonstrate that knockout of PATJ in epithelial cells results in tight junction defects as well as in a disturbed apical-basal polarity and impaired lumen formation in three-dimensional cyst assays. Mechanistically, we found PATJ to associate with and inhibit histone deacetylase 7 (HDAC7). Inhibition or downregulation of HDAC7 restores polarity and lumen formation. Gene expression analysis of PATJ-deficient cells revealed an impaired expression of genes involved in cell junction assembly and membrane organization, which is rescued by the downregulation of HDAC7. Notably, the function of PATJ regulating HDAC7-dependent cilia formation does not depend on its canonical interaction partner, Pals1, indicating a new role of PATJ, which is distinct from its function in the Crumbs complex. By contrast, polarity and lumen phenotypes observed in Pals1- and PATJ-deficient epithelial cells can be rescued by inhibition of HDAC7, suggesting that the main function of this polarity complex in this process is to modulate the transcriptional profile of epithelial cells by inhibiting HDAC7. © 2023. The Author(s).
Julia Fiedler, Thomas Moennig, Johanna H Hinrichs, Annika Weber, Thomas Wagner, Tim Hemmer, Rita Schröter, Thomas Weide, Daniel Epting, Carsten Bergmann, Pavel Nedvetsky, Michael P Krahn. PATJ inhibits histone deacetylase 7 to control tight junction formation and cell polarity. Cellular and molecular life sciences : CMLS. 2023 Oct 25;80(11):333
PMID: 37878054
View Full Text