USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components

Commun Biol. 2022 Apr 19;5(1):378. doi: 10.1038/s42003-022-03254-7.

Abstract

Previously, we have shown that the translocation of Grainyhead-like 3 (GRHL3) transcription factor from the nucleus to the cytoplasm triggers the switch from canonical Wnt signaling for epidermal differentiation to non-canonical Wnt signaling for epithelial morphogenesis. However, the molecular mechanism that underlies the cytoplasmic localization of GRHL3 protein and that activates non-canonical Wnt signaling is not known. Here, we show that ubiquitin-specific protease 39 (USP39), a deubiquitinating enzyme, is involved in the subcellular localization of GRHL3 as a potential GRHL3-interacting protein and is necessary for epithelial morphogenesis to up-regulate expression of planar cell polarity (PCP) components. Notably, mouse Usp39-deficient embryos display early embryonic lethality due to a failure in primitive streak formation and apico-basal polarity in epiblast cells, resembling those of mutant embryos of the Prickle1 gene, a crucial PCP component. Current findings provide unique insights into how differentiation and morphogenesis are coordinated to construct three-dimensional complex structures via USP39.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Cell Differentiation
  • Cell Polarity* / physiology
  • DNA-Binding Proteins / metabolism
  • LIM Domain Proteins
  • Mammals
  • Mice
  • Morphogenesis
  • Transcription Factors* / metabolism
  • Up-Regulation

Substances

  • Adaptor Proteins, Signal Transducing
  • DNA-Binding Proteins
  • Grhl3 protein, mouse
  • LIM Domain Proteins
  • Prickle1 protein, mouse
  • Transcription Factors