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 Blood, 1 September 2008, Vol. 112, No. 5, pp. 2062-2070.
Prepublished online as a Blood First Edition Paper on June 11, 2008; DOI 10.1182/blood-2008-04-152710.

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Submitted April 23, 2008
Accepted May 14, 2008

HES1 is a novel interactor of the Fanconi anemia core complex

Cedric S Tremblay, Feng Fei Huang, Ouassila Habi, Caroline C Huard, Chantal Godin, Georges Levesque, and Madeleine Carreau*

Unite de recherche en Pediatrie, Centre de recherche du CHUL, Quebec, QC, Canada
Unite de Neurosciences, Centre de recherche du CHUL, Quebec, QC, Canada
Departement de Biologie Medicale, Universite Laval, Quebec, QC, Canada
Departement de Pediatrie, Universite Laval, Quebec, QC, Canada

* Corresponding author; email: madeleine.carreau{at}crchul.ulaval.ca.

Fanconi Anemia (FA) proteins are thought to play a role in chromosome stability and repair of DNA crosslinks; however, these functions may not fully explain the developmental abnormalities and bone marrow failure that are characteristic of FA individuals. Here we associate the FA proteins with the Notch1 developmental pathway through a direct protein-protein interaction between the FA core complex and the Hairy Enhancer of Split 1 (HES1). HES1 interaction with FA core complex members is dependant on a functional FA pathway. Cells depleted of HES1 exhibit an FA-like phenotype that includes cellular hypersensitivity to MMC and lack of FANCD2 monoubiquitination and foci formation. HES1 is also required for proper nuclear localization or stability of some members of the core complex. Our results suggest that HES1 is a novel interacting protein of the FA core complex.


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C. S. Tremblay, C. C. Huard, F.-F. Huang, O. Habi, V. Bourdages, G. Levesque, and M. Carreau
The Fanconi Anemia Core Complex Acts as a Transcriptional Co-regulator in Hairy Enhancer of Split 1 Signaling
J. Biol. Chem., May 15, 2009; 284(20): 13384 - 13395.
[Abstract] [Full Text] [PDF]


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