FAN1 acts with FANCI-FANCD2 to promote DNA interstrand cross-link repair

Science. 2010 Aug 6;329(5992):693-6. doi: 10.1126/science.1192656. Epub 2010 Jul 29.

Abstract

Fanconi anemia (FA) is caused by mutations in 13 Fanc genes and renders cells hypersensitive to DNA interstrand cross-linking (ICL) agents. A central event in the FA pathway is mono-ubiquitylation of the FANCI-FANCD2 (ID) protein complex. Here, we characterize a previously unrecognized nuclease, Fanconi anemia-associated nuclease 1 (FAN1), that promotes ICL repair in a manner strictly dependent on its ability to accumulate at or near sites of DNA damage and that relies on mono-ubiquitylation of the ID complex. Thus, the mono-ubiquitylated ID complex recruits the downstream repair protein FAN1 and facilitates the repair of DNA interstrand cross-links.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Cell Line
  • Cell Nucleus / metabolism
  • DNA / metabolism*
  • DNA Damage
  • DNA Repair*
  • Endodeoxyribonucleases
  • Exodeoxyribonucleases / chemistry
  • Exodeoxyribonucleases / genetics
  • Exodeoxyribonucleases / metabolism*
  • Fanconi Anemia Complementation Group D2 Protein / metabolism*
  • Fanconi Anemia Complementation Group Proteins / metabolism*
  • Gene Knockdown Techniques
  • HeLa Cells
  • Humans
  • Mitomycin / pharmacology
  • Molecular Sequence Data
  • Multifunctional Enzymes
  • Mutant Proteins / metabolism
  • Protein Binding
  • Ubiquitinated Proteins / metabolism
  • Ubiquitination
  • Zinc Fingers

Substances

  • FANCD2 protein, human
  • FANCI protein, human
  • Fanconi Anemia Complementation Group D2 Protein
  • Fanconi Anemia Complementation Group Proteins
  • Multifunctional Enzymes
  • Mutant Proteins
  • Ubiquitinated Proteins
  • Mitomycin
  • DNA
  • Endodeoxyribonucleases
  • Exodeoxyribonucleases
  • FAN1 protein, human