Translocation t(2;11) in CLL cells results in CXCR4/MAML2 fusion oncogene

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Abstract

Recent investigations of chromosomal aberrations in chronic lymphocytic leukemia (CLL) led to a better understanding of the molecular causes of CLL. Here we report a rearrangement between MAML2 (mastermind-like protein 2) and CXCR4 (specific receptor for CXC chemokine stromal cell-derived factor-1) in CLL cells of a patient with a t(2;11)(q22.1;q21) chromosomal translocation. The rearrangement between MAML2 and CXCR4, created by a t(2;11)(q22.1;q21) translocation, results in a new fusion gene in which a portion of CXCR4 is linked to the MAML2 gene. This fusion gene encodes for CXCR4/MAML2 protein chimera in which the N-terminal basic domain of MAML2 is replaced by the N-terminal domain of CXCR4. © 2014 by The American Society of Hematology.

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Acunzo, M., Romano, G., Wernicke, D., Balatti, V., Rassenti, L. Z., Dell’Aquila, M., … Croce, C. M. (2014). Translocation t(2;11) in CLL cells results in CXCR4/MAML2 fusion oncogene. Blood, 124(2), 259–262. https://doi.org/10.1182/blood-2014-02-554675

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