MLL5 contributes to hematopoietic stem cell fitness and homeostasis.

Journal:

Blood 2009 Feb

Authors:

Zhang Y, Wong J, Klinger M, Tran MT, Shannon KM, Killeen N

Abstract

MLL5 is a novel trithorax group gene and a candidate tumor suppressor gene located within a 2.5-Mb interval of chromosome band 7q22 that frequently is deleted in human myeloid malignancy. Here we show that inactivation of the Mll5 gene in mice results in a 30% reduction in the average representation of hematopoietic stem cells and in functional impairment of long-term hematopoietic repopulation potential under competitive conditions. Bone marrow cells from Mll5-deficient mice were defective in s
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pleen colony-forming assays, and the mutant mice showed enhanced susceptibility to 5-fluorouracil-induced myelosuppression. Heterozygous and homozygous Mll5 mutant mice did not spontaneously develop hematologic cancers, and loss of Mll5 did not alter the phenotype of a fatal myeloproliferative disorder induced by oncogenic Kras in vivo. Collectively, the data reveal an important role for Mll5 in HSC homeostasis and provide a basis for further studies to explore its role in leukemogenesis.[less]

Mesh Headings:

Animals, Antimetabolites, Antineoplastic, Apoptosis, Bone Marrow Transplantation, Cell Cycle, Cell Differentiation, Fluorouracil, Gene Expression, Hematopoiesis, Hematopoietic Stem Cells, Histone-Lysine N-Methyltransferase, Homeostasis, Integrases, Leukemia, Mice, Mice, Inbred C57BL, Mice, Knockout, Multipotent Stem Cells, Myeloid-Lymphoid Leukemia Protein, Proto-Oncogene Proteins p21(ras), Spleen