2A-DUB/Mysm1 Regulates Epidermal Development in Part by Suppressing p53-Mediated Programs

Int J Mol Sci. 2018 Feb 28;19(3):687. doi: 10.3390/ijms19030687.

Abstract

Development and homeostasis of the epidermis are governed by a complex network of sequence-specific transcription factors and epigenetic modifiers cooperatively regulating the subtle balance of progenitor cell self-renewal and terminal differentiation. To investigate the role of histone H2A deubiquitinase 2A-DUB/Mysm1 in the skin, we systematically analyzed expression, developmental functions, and potential interactions of this epigenetic regulator using Mysm1-deficient mice and skin-derived epidermal cells. Morphologically, skin of newborn and young adult Mysm1-deficient mice was atrophic with reduced thickness and cellularity of epidermis, dermis, and subcutis, in context with altered barrier function. Skin atrophy correlated with reduced proliferation rates in Mysm1-/- epidermis and hair follicles, and increased apoptosis compared with wild-type controls, along with increases in DNA-damage marker γH2AX. In accordance with diminished α6-Integrinhigh+CD34⁺ epidermal stem cells, reduced colony formation of Mysm1-/- epidermal progenitors was detectable in vitro. On the molecular level, we identified p53 as potential mediator of the defective Mysm1-deficient epidermal compartment, resulting in increased pro-apoptotic and anti-proliferative gene expression. In Mysm1-/-p53-/- double-deficient mice, significant recovery of skin atrophy was observed. Functional properties of Mysm1-/- developing epidermis were assessed by quantifying the transepidermal water loss. In summary, this investigation uncovers a role for 2A-DUB/Mysm1 in suppression of p53-mediated inhibitory programs during epidermal development.

Keywords: DUB; Mysm1; apoptosis; epidermal barrier; epidermal stem cell; epigenetics; histone modification; p53; p63; skin.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Atrophy
  • Endopeptidases / genetics
  • Endopeptidases / metabolism*
  • Epidermis / embryology*
  • Epidermis / metabolism*
  • Epidermis / pathology
  • Gene Expression
  • Genotype
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • Stem Cells / metabolism
  • Trans-Activators
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Ubiquitin-Specific Proteases

Substances

  • Trans-Activators
  • Tumor Suppressor Protein p53
  • Endopeptidases
  • MYSM1 protein, mouse
  • Ubiquitin-Specific Proteases