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Fusion of the Homeobox Gene HLXB9 and the ETV6 Gene in Infant Acute Myeloid Leukemias with the t(7;12)(q36;p13)¹

Departments of Cell Biology and Genetics [H. B. B., E. v. D., R. S.] and Clinical Genetics [A. d. K., R. S.], Erasmus University Rotterdam, 3000 DR Rotterdam, the Netherlands; Dutch Childhood Leukemia Study Group, 2504 AM The Hague, the Netherlands [E. v. W.]; and Department of Clinical Genetics, University Hospital, SE-22185 Lund, Sweden [I. P., M. I., B. J.]

Recently, we and others reported a recurrent t(7;12)(q36;p13) found in myeloid malignancies in children 18 months of age and associated with a poor prognosis. Fluorescence in situ hybridization studies mapped the 12p13 breakpoint to the first intron of ETV6 and narrowed down the region of 7q36 involved. By using the sequences made public recently by the Human Genome Project, two candidate genes in 7q36 were identified: the homeobox gene HLXB9 and c7orf3, a gene with unknown function. Reverse transcription-PCR of two cases with t(7;12), using primers for c7orf3 and ETV6, was negative. However, reverse transcription-PCR for HLXB9-ETV6 demonstrated alternative splicing; the two major bands corresponded to fusion of exon 1 of HLXB9 to exons 2 and 3, respectively, of ETV6. The reciprocal ETV6-HLXB9 transcript was not detected. It remains to be elucidated if the leukemic phenotype is attributable to the formation of the HLXB9-ETV6 fusion protein, which includes the helix-loop-helix and E26 transformation-specific DNA binding domains of ETV6 or to the disruption of the normal ETV6 protein.

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