FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway. Academic Article uri icon

Overview

abstract

  • Fanconi anemia (FA) nuclear core complex is a multiprotein complex required for the functional integrity of the FA-BRCA pathway regulating DNA repair. This pathway is inactivated in FA, a devastating genetic disease, which leads to hematologic defects and cancer in patients. Here we report the isolation and characterization of a novel 20-kDa FANCA-associated protein (FAAP20). We show that FAAP20 is an integral component of the FA nuclear core complex. We identify a region on FANCA that physically interacts with FAAP20, and show that FANCA regulates stability of this protein. FAAP20 contains a conserved ubiquitin-binding zinc-finger domain (UBZ), and binds K-63-linked ubiquitin chains in vitro. The FAAP20-UBZ domain is not required for interaction with FANCA, but is required for DNA-damage-induced chromatin loading of FANCA and the functional integrity of the FA pathway. These findings reveal critical roles for FAAP20 in the FA-BRCA pathway of DNA damage repair and genome maintenance.

publication date

  • February 17, 2012

Research

keywords

  • DNA Repair
  • Fanconi Anemia
  • Fanconi Anemia Complementation Group Proteins
  • Signal Transduction
  • Ubiquitin

Identity

PubMed Central ID

  • PMC3321854

Scopus Document Identifier

  • 84859564894

Digital Object Identifier (DOI)

  • 10.1182/blood-2011-10-385963

PubMed ID

  • 22343915

Additional Document Info

volume

  • 119

issue

  • 14