The translocation t (8; 16)(p11; p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

J Borrow, VP Stanton Jr, JM Andresen, R Becher… - Nature …, 1996 - nature.com
J Borrow, VP Stanton Jr, JM Andresen, R Becher, FG Behm, RSK Chaganti, CI Civin
Nature genetics, 1996nature.com
Abstract The recurrent translocation t (8; 16)(p11; p13) is a cytogenetic hallmark for the
M4/M5 subtype of acute myeloid leukaemia. Here we identify the breakpoint-associated
genes. Positional cloning on chromosome 16 implicates the CREB-binding protein (CBP), a
transcriptional adaptor/coactivator protein. At the chromosome 8 breakpoint we identify a
novel gene, MOZ, which encodes a 2,004-amino-acid protein characterized by two C4HC3
zinc fingers and a single C2HC zinc finger in conjunction with a putative acetyltransferase …
Abstract
The recurrent translocation t(8;16)(p11 ;p13) is a cytogenetic hallmark for the M4/M5 subtype of acute myeloid leukaemia. Here we identify the breakpoint-associated genes. Positional cloning on chromosome 16 implicates the CREB-binding protein (CBP), a transcriptional adaptor/coactivator protein. At the chromosome 8 breakpoint we identify a novel gene, MOZ, which encodes a 2,004-amino-acid protein characterized by two C4HC3 zinc fingers and a single C2HC zinc finger in conjunction with a putative acetyltransferase signature. In-frame MOZ–CBP fusion transcripts combine the MOZ finger motifs and putative acetyltransferase domain with a largely intact CBP. We suggest that MOZ may represent a chromatin-associated acetyltransferase, and raise the possibility that a dominant MOZ–CBP fusion protein could mediate leukaemogenesis via aberrant chromatin acetylation.
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