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Published on: August 12, 2015
The downregulation of BAP1 expression by BCR-ABL reduces the stability of BRCA1 in chronic myeloid leukemia
Fatima Dkhissi1, Djamel Aggoune2, Julien Pontis3
1Institut national U935 de la santé et de la recherche médicale, Université de Poitiers, Poitiers, France; Laboratoire Epigénétique et Destin Cellulaire, CNRS-UMR 7216 Université Paris Diderot, Sorbonne Paris Cité, Paris, France; Laboratoire Signalisation et Transports Ioniques Membranaires, CNRS-ERL 7368 Université de Poitiers, Poitiers, France.
Abstract:
BCR-ABL induces an intrinsic genetic instability in chronic myeloid leukemia (CML). The protein breast cancer 1, early onset (BRCA1)-associated protein 1 (BAP1) is a deubiquitinase interacting with the DNA repair regulator BRCA1 and is frequently inactivated in many cancers. Here, we report that BAP1 mRNA and protein levels are downregulated in a BCR-ABL1-expressing hematopoietic cell line (UT-7/11). A decrease of BAP1 transcripts is also observed in newly diagnosed CML patients. Moreover, BAP1 protein levels are low or undetectable in CD34(+) cells from CML patients at diagnosis as compared with CD34(+) cells from normal donors. In addition, BRCA1 protein level is reduced in BCR-ABL1-expressing UT-7/11 cells. Finally, the enforced expression of BAP1 is associated with BRCA1 protein deubiquitination and restoration. These results demonstrate BAP1 as a major link with the BCR-ABL-induced downregulation of BRCA1 in CML.
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