Polycomb-like Proteins in Gene Regulation and Cancer

Genes (Basel). 2023 Apr 18;14(4):938. doi: 10.3390/genes14040938.

Abstract

Polycomb-like proteins (PCLs) are a crucial group of proteins associated with the Polycomb repressive complex 2 (PRC2) and are responsible for setting up the PRC2.1 subcomplex. In the vertebrate system, three homologous PCLs exist: PHF1 (PCL1), MTF2 (PCL2), and PHF19 (PCL3). Although the PCLs share a similar domain composition, they differ significantly in their primary sequence. PCLs play a critical role in targeting PRC2.1 to its genomic targets and regulating the functionality of PRC2. However, they also have PRC2-independent functions. In addition to their physiological roles, their dysregulation has been associated with various human cancers. In this review, we summarize the current understanding of the molecular mechanisms of the PCLs and how alterations in their functionality contribute to cancer development. We particularly highlight the nonoverlapping and partially opposing roles of the three PCLs in human cancer. Our review provides important insights into the biological significance of the PCLs and their potential as therapeutic targets for cancer treatment.

Keywords: MTF2; PHF1; PHF19; Polycomb repressive complex 2; Polycomb-like; cancer; chromatin; epigenetics; leukemia; transcription.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleus / metabolism
  • Drosophila Proteins* / metabolism
  • Histones / genetics
  • Humans
  • Neoplasms* / genetics
  • Polycomb Repressive Complex 1 / metabolism
  • Polycomb Repressive Complex 2 / genetics
  • Polycomb-Group Proteins / genetics
  • Polycomb-Group Proteins / metabolism

Substances

  • Histones
  • Polycomb-Group Proteins
  • Polycomb Repressive Complex 2
  • Polycomb Repressive Complex 1
  • Drosophila Proteins

Grants and funding

This work was supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation, 416910386, 516068166) and the Fritz Thyssen Foundation (10.20.1.005MN).