Article open access publication

Fbxl10 overexpression in murine hematopoietic stem cells induces leukemia involving metabolic activation and upregulation of Nsg2

Blood, American Society of Hematology, ISSN 1528-0020

Volume 125, 22, 2015

DOI:10.1182/blood-2014-03-562694, Dimensions: pub.1035435150, PMC: PMC4447860, PMID: 25872778,

Affiliations

Organisations

  1. (1) Department of Disease Model and
  2. (2) Hiroshima University, grid.257022.0
  3. (3) Keio University, grid.26091.3c
  4. (4) Chiba University, grid.136304.3
  5. (5) Tokyo Women's Medical University, grid.410818.4
  6. (6) Center for Cancer Research, grid.417768.b
  7. (7) Ochanomizu University, grid.412314.1
  8. (8) Biotech Research and Innovation Centre (BRIC) and
  9. (9) University of Copenhagen, grid.5254.6, KU

Description

We previously reported that deficiency for Samd9L, which was cloned as a candidate gene for -7/7q- syndrome, accelerated leukemia cooperatively with enhanced expression of a histone demethylase: F-box and leucine-rich repeat protein 10 (Fbxl10, also known as Jhdm1b, Kdm2b, and Ndy1). To further investigate the role of Fbxl10 in leukemogenesis, we generated transgenic (Tg) mice that overexpress Fbxl10 in hematopoietic stem cells (HSCs). Interestingly, Fbxl10 Tg mice developed myeloid or B-lymphoid leukemia with complete penetrance. HSCs from the Tg mice exhibited an accelerated G0/G1-to-S transition with a normal G0 to G1 entry, resulting in pleiotropic progenitor cell expansion. Fbxl10 Tg HSCs displayed enhanced expression of neuron-specific gene family member 2 (Nsg2), and forced expression of Nsg2 in primary bone marrow cells resulted in expansion of immature cells. In addition, the genes involved in mitochondrial oxidative phosphorylation were markedly enriched in Fbxl10 Tg HSCs, coupled with increased cellular adenosine 5'-triphosphate levels. Moreover, chromatin immunoprecipitation followed by sequencing analysis demonstrated that Fbxl10 directly binds to the regulatory regions of Nsg2 and oxidative phosphorylation genes. These findings define Fbxl10 as a bona fide oncogene, whose deregulated expression contributes to the development of leukemia involving metabolic proliferative advantage and Nsg2-mediated impaired differentiation.

Funders

Research Categories

Main Subject Area

Fields of Research

Links & Metrics

NORA University Profiles

University of Copenhagen

Dimensions Citation Indicators

Times Cited: 36

Field Citation Ratio (FCR): 13.84

Relative Citation ratio (RCR): 1.19

Open Access Info

Bronze