H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor β gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22)

• Published in: Blood 2001-06, Vol.97 (12), p.3910-3918
• Main Authors: Schwaller, Juerg, Anastasiadou, Ema, Cain, Danielle, Kutok, Jeff, Wojiski, Sarah, Williams, Ifor R., LaStarza, Roberta, Crescenzi, Barbara, Sternberg, David W., Andreasson, Patrick, Schiavo, Roberta, Siena, Salvatore, Mecucci, Cristina, Gilliland, D. Gary
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Carcinoma, Papillary - genetics; Cell Transformation, Neoplastic - genetics; Chromosomes, Human, Pair 10 - genetics; Chromosomes, Human, Pair 5 - genetics; Cloning, Molecular; Cytogenetic Analysis; Cytoskeletal Proteins; DNA, Neoplasm - genetics; DNA, Neoplasm - isolation & purification; Gene Rearrangement; Hematologic and hematopoietic diseases; Humans; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - etiology; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis; Medical sciences; Mutagenesis; Myeloid Cells - metabolism; Myeloid Cells - pathology; Oncogene Proteins, Fusion; Protein Structure, Tertiary; Proteins - genetics; Proteins - metabolism; Receptor, Platelet-Derived Growth Factor beta - genetics; Thyroid Neoplasms - genetics; Transfection; Translocation, Genetic
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood.V97.12.3910

The molecular cloning of the t(5;10)(q33;q22) associated with atypical chronic myeloid leukemia (CML) is reported. Fluorescence in situ hybridization (FISH), Southern blot, and reverse transcriptase– polymerase chain reaction analysis demonstrated that the translocation resulted in an H4/platelet-derived growth factor receptor βR (PDGFβR) fusion transcript that incorporated 5′ sequences from H4 fused in frame to 3′PDGFβR sequences encoding the transmembrane, WW-like, and tyrosine kinase domains. FISH combined with immunophenotype analysis showed that t(5;10)(q33;q22) was present in CD13+ and CD14+ cells but was not observed in CD3+ or CD19+ cells. H4 has previously been implicated in pathogenesis of papillary thyroid carcinoma as a fusion partner of RET. The H4/RET fusion incorporates 101 amino acids of H4, predicted to encode a leucine zipper dimerization domain, whereas the H4/PDGFβR fusion incorporated an additional 267 amino acids of H4. Retroviral transduction of H4/PDGFβR, but not a kinase-inactive mutant, conferred factor-independent growth to Ba/F3 cells and caused a T-cell lymphoblastic lymphoma in a murine bone marrow transplantation assay of transformation. Mutational analysis showed that the amino-terminal H4 leucine zipper domain (amino acids 55-93), as well as H4 amino acids 101 to 386, was required for efficient induction of factor-independent growth of Ba/F3 cells. Tryptophan-to-alanine substitutions in the PDGFβR WW-like domain at positions 566/593, or tyrosine-to-phenylalanine substitutions at PDGFβR positions 579/581 impaired factor-independent growth of Ba/F3 cells. H4/PDGFβR is an oncoprotein expressed in t(5;10)(q33;q22) atypical CML and requires dimerization motifs in the H4 moiety, as well as residues implicated in signal transduction by PDGFβR, for efficient induction of factor-independent growth of Ba/F3 cells.