Molecular Regulation of the Polycomb Repressive-Deubiquitinase

Int J Mol Sci. 2020 Oct 22;21(21):7837. doi: 10.3390/ijms21217837.

Abstract

Post-translational modification of histone proteins plays a major role in histone-DNA packaging and ultimately gene expression. Attachment of ubiquitin to the C-terminal tail of histone H2A (H2AK119Ub in mammals) is particularly relevant to the repression of gene transcription, and is removed by the Polycomb Repressive-Deubiquitinase (PR-DUB) complex. Here, we outline recent advances in the understanding of PR-DUB regulation, which have come through structural studies of the Drosophila melanogaster PR-DUB, biochemical investigation of the human PR-DUB, and functional studies of proteins that associate with the PR-DUB. In humans, mutations in components of the PR-DUB frequently give rise to malignant mesothelioma, melanomas, and renal cell carcinoma, and increase disease risk from carcinogens. Diverse mechanisms may underlie disruption of the PR-DUB across this spectrum of disease. Comparing and contrasting the PR-DUB in mammals and Drosophila reiterates the importance of H2AK119Ub through evolution, provides clues as to how the PR-DUB is dysregulated in disease, and may enable new treatment approaches in cancers where the PR-DUB is disrupted.

Keywords: H2AK119Ub; PR-DUB; Polycomb Repressive-Deubiquitinase.

Publication types

  • Review

MeSH terms

  • Animals
  • Deubiquitinating Enzymes / genetics
  • Deubiquitinating Enzymes / metabolism*
  • Drosophila Proteins / metabolism
  • Evolution, Molecular
  • Haploinsufficiency / genetics
  • Histones / metabolism
  • Humans
  • Mammals
  • Microtubule-Associated Proteins / metabolism
  • Multiprotein Complexes / chemistry
  • Multiprotein Complexes / metabolism
  • Mutation
  • Neoplasms / genetics
  • Polycomb-Group Proteins / genetics
  • Polycomb-Group Proteins / metabolism*
  • Repressor Proteins / metabolism
  • Transcription Factors / metabolism
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin Thiolesterase / genetics
  • Ubiquitin Thiolesterase / metabolism

Substances

  • ASX protein, Drosophila
  • ASXL3 protein, human
  • BAP1 protein, human
  • Drosophila Proteins
  • Feo protein, Drosophila
  • Histones
  • Microtubule-Associated Proteins
  • Multiprotein Complexes
  • Polycomb-Group Proteins
  • Repressor Proteins
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Deubiquitinating Enzymes
  • UCHL5 protein, human
  • Ubiquitin Thiolesterase
  • calypso protein, Drosophila