The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Nat Genet. 2005 Sep;37(9):931-3. doi: 10.1038/ng1624. Epub 2005 Aug 21.

Abstract

Seven Fanconi anemia-associated proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG and FANCL) form a nuclear Fanconi anemia core complex that activates the monoubiquitination of FANCD2, targeting FANCD2 to BRCA1-containing nuclear foci. Cells from individuals with Fanconi anemia of complementation groups D1 and J (FA-D1 and FA-J) have normal FANCD2 ubiquitination. Using genetic mapping, mutation identification and western-blot data, we identify the defective protein in FA-J cells as BRIP1 (also called BACH1), a DNA helicase that is a binding partner of the breast cancer tumor suppressor BRCA1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blotting, Western
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Nucleus
  • Chromosomes, Human, Pair 17*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Fanconi Anemia / genetics*
  • Fanconi Anemia Complementation Group C Protein
  • Fanconi Anemia Complementation Group D2 Protein
  • Fanconi Anemia Complementation Group Proteins
  • Female
  • Humans
  • Male
  • Microsatellite Repeats
  • Mutation / genetics*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Pedigree
  • Polymorphism, Single Nucleotide*
  • RNA Helicases / genetics*
  • RNA Helicases / metabolism
  • Ubiquitin / metabolism*

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • FANCC protein, human
  • FANCD2 protein, human
  • Fanconi Anemia Complementation Group C Protein
  • Fanconi Anemia Complementation Group D2 Protein
  • Fanconi Anemia Complementation Group Proteins
  • Nuclear Proteins
  • Ubiquitin
  • BRIP1 protein, human
  • RNA Helicases