Abstract
Chromosomal translocations involving the mixed lineage leukemia (MLL) gene are associated with aggressive acute lymphoid and myeloid leukemias. These translocations are restricted to an 8.3-kb breakpoint region resulting in fusion of amino terminal MLL sequences in frame to 1 of more than 60 different translocation partners. The translocations consistently delete the plant homeodomain (PHD) fingers and more carboxyl terminal MLL sequences. The function of the PHD fingers is obscure and their specific role in transformation has not been explored. Here we show that inclusion of the PHD fingers in the MLL fusion protein MLL-AF9 blocked immortalization of hematopoietic progenitors. Inclusion of 2 or more PHD fingers reduced association with the Hoxa9 locus and suppressed Hoxa9 up-regulation in hematopoietic progenitors. These data provide an explanation for why MLL translocation breakpoints exclude the PHD fingers and suggest a possible role for these domains in regulating the function of wild-type MLL.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bone Marrow Cells / drug effects
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Bone Marrow Cells / pathology
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Cell Transformation, Neoplastic / drug effects
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Cell Transformation, Neoplastic / genetics*
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Cells, Cultured
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Genes, Transgenic, Suicide / genetics
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Genes, Tumor Suppressor / physiology
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Hematopoiesis / genetics
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Histone-Lysine N-Methyltransferase
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Homeodomain Proteins / chemistry
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Homeodomain Proteins / genetics
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Homeodomain Proteins / pharmacology
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Homeodomain Proteins / physiology
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Mice
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Mice, Inbred C57BL
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Myeloid-Lymphoid Leukemia Protein / antagonists & inhibitors*
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Myeloid-Lymphoid Leukemia Protein / chemistry
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Myeloid-Lymphoid Leukemia Protein / genetics
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Myeloid-Lymphoid Leukemia Protein / physiology*
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Oncogene Proteins, Fusion / antagonists & inhibitors*
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Oncogene Proteins, Fusion / genetics
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Oncogene Proteins, Fusion / physiology
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Protein Structure, Tertiary / genetics
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Protein Structure, Tertiary / physiology
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Transduction, Genetic
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Tumor Stem Cell Assay
Substances
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Homeodomain Proteins
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KMT2A protein, human
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MLL-AF9 fusion protein, human
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Oncogene Proteins, Fusion
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Myeloid-Lymphoid Leukemia Protein
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Histone-Lysine N-Methyltransferase