FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex

Maya Raghunandan, Indrajit Chaudhury, Stephanie L. Kelich, Helmut Hanenberg, Alexandra Sobeck

Research output: Contribution to journalArticlepeer-review

38 Scopus citations


Fanconi Anemia (FA) is an inherited multi-gene cancer predisposition syndrome that is characterized on the cellular level by a hypersensitivity to DNA interstrand crosslinks (ICLs). To repair these lesions, the FA pathway proteins are thought to act in a linear hierarchy: Following ICL detection, an upstream FA core complex monoubiquitinates the central FA pathway members FANCD2 and FANCI, followed by their recruitment to chromatin. Chromatin-bound monoubiquitinated FANCD2 and FANCI subsequently coordinate DNA repair factors including the downstream FA pathway members FANCJ and FANCD1/BRCA2 to repair the DNA ICL. Importantly, we recently showed that FANCD2 has additional independent roles: it binds chromatin and acts in concert with the BLM helicase complex to promote the restart of aphidicolin (APH)-stalled replication forks, while suppressing the firing of new replication origins. Here, we show that FANCD2 fulfills these roles independently of the FA core complex-mediated monoubiquitination step. Following APH treatment, nonubiquitinated FANCD2 accumulates on chromatin, recruits the BLM complex, and promotes robust replication fork recovery regardless of the absence or presence of a functional FA core complex. In contrast, the downstream FA pathway members FANCJ and BRCA2 share FANCD2's role in replication fork restart and the suppression of new origin firing. Our results support a non-linear FA pathway model at stalled replication forks, where the nonubiquitinated FANCD2 isoform - in concert with FANCJ and BRCA2 - fulfills a specific function in promoting efficient replication fork recovery independently of the FA core complex.

Original languageEnglish (US)
Pages (from-to)342-353
Number of pages12
JournalCell Cycle
Issue number3
StatePublished - Feb 1 2015

Bibliographical note

Funding Information:
AS was supported by the National Science Foundation (award 1121023) and the American Cancer Society (RSG-13-039-01-DMC). HH was supported by the NIH R01 CA155294-04 and by the BMBF grant “FoneFA.” In addition, this work was also partly supported by a Brainstorm Award from the Masonic Cancer Center at the University of Minnesota.

Publisher Copyright:
© 2015 Taylor & Francis Group, LLC.


  • FA pathway
  • FANCD2
  • FANCD2 monoubiquitination
  • Fanconi anemia
  • Replication fork recovery


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