Pbx1 is a downstream target of Evi-1 in hematopoietic stem/progenitors and leukemic cells

被引:55
|
作者
Shimabe, M. [1 ]
Goyama, S. [1 ]
Watanabe-Okochi, N. [1 ]
Yoshimi, A. [1 ]
Ichikawa, M. [1 ]
Imai, Y. [1 ]
Kurokawa, M. [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, Tokyo 1138655, Japan
基金
日本学术振兴会;
关键词
Evi-1; Pbx1; leukemogenesis; target gene; MYELOID-TRANSFORMING GENE; DNA-BINDING; STEM-CELLS; PRE-B; TRANSCRIPTION FACTOR-1; TRANSLOCATION PROTEIN; ZINC FINGERS; SELF-RENEWAL; IDENTIFICATION; SEQUENCE;
D O I
10.1038/onc.2009.288
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ecotropic viral integration site-1 (Evi-1) is a nuclear transcription factor, which is essential for the proliferation/maintenance of hematopoietic stem cells (HSCs). Aberrant expression of Evi-1 has been frequently found in myeloid leukemia, and is associated with a poor patient survival. Recently, we reported candidate target genes of Evi-1 shared in HSCs and leukemic cells using gene expression profiling analysis. In this study, we identified Pbx1, a proto-oncogene in hematopoietic malignancy, as a target gene of Evi-1. Overexpression of Evi-1 increased Pbx1 expression in hematopoietic stem/progenitor cells. An analysis of the Pbx1 promoter region revealed that Evi-1 upregulates Pbx1 transcription. Furthermore, reduction of Pbx1 levels through RNAi-mediated knockdown significantly inhibited Evi-1-induced transformation. In contrast, knockdown of Pbx1 did not impair bone marrow transformation by E2A/HLF or AML1/ETO, suggesting that Pbx1 is specifically required for the maintenance of bone marrow transformation mediated by Evi-1. These results indicate that Pbx1 is a target gene of Evi-1 involved in Evi-1-mediated leukemogenesis. Oncogene (2009) 28, 4364-4374; doi: 10.1038/onc.2009.288; published online 21 September 2009
引用
收藏
页码:4364 / 4374
页数:11
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