The core binding factor beta subunit (CBF beta) is the non-DNA binding subu
nit of the core-binding factors, transcription factors essential for multip
le developmental processes including hematopoiesis and bone development. Ch
romosomal translocations involving the human CBFB gene are associated with
a large percentage of human leukemias. The N-terminal 141 amino acids of CB
F beta contains the heterodimerization domain for the DNA-binding CBF alpha
subunits, and is sufficient for CBF beta function in vivo. Here we present
the high-resolution solution structure of the CBF beta heterodimerization
domain. It is a novel alpha/beta structure consisting of two three-stranded
beta-sheets packed on one another in a sandwich arrangement, with four per
ipheral alpha-helices. The CBF alpha binding site on CBF beta has been mapp
ed by chemical shift perturbation analysis.