BRCA1-A and BRISC: Multifunctional Molecular Machines for Ubiquitin Signaling

Biomolecules. 2020 Oct 31;10(11):1503. doi: 10.3390/biom10111503.

Abstract

The K63-linkage specific deubiquitinase BRCC36 forms the core of two multi-subunit deubiquitination complexes: BRCA1-A and BRISC. BRCA1-A is recruited to DNA repair foci, edits ubiquitin signals on chromatin, and sequesters BRCA1 away from the site of damage, suppressing homologous recombination by limiting resection. BRISC forms a complex with metabolic enzyme SHMT2 and regulates the immune response, mitosis, and hematopoiesis. Almost two decades of research have revealed how BRCA1-A and BRISC use the same core of subunits to perform very distinct biological tasks.

Keywords: BRCA1; BRCC36; DNA repair; RAP80; SHMT2; SUMO; deubiquitination; immune regulation; ubiquitin.

Publication types

  • Review

MeSH terms

  • BRCA1 Protein / genetics*
  • Chromatin / genetics
  • DNA Repair / genetics*
  • DNA-Binding Proteins / genetics
  • Deubiquitinating Enzymes / genetics*
  • Glycine Hydroxymethyltransferase / genetics*
  • Hematopoiesis / genetics
  • Histone Chaperones / genetics
  • Humans
  • Immunity / genetics
  • Mitosis / genetics
  • SUMO-1 Protein / genetics
  • Ubiquitin / genetics

Substances

  • BRCA1 Protein
  • BRCA1 protein, human
  • Chromatin
  • DNA-Binding Proteins
  • Histone Chaperones
  • SUMO-1 Protein
  • UIMC1 protein, human
  • Ubiquitin
  • Glycine Hydroxymethyltransferase
  • SHMT protein, human
  • BRCC3 protein, human
  • Deubiquitinating Enzymes