Oncogenic transcription factor Evi1 regulates hematopoietic stem cell proliferation through GATA-2 expression

被引:175
作者
Yuasa, H
Oike, Y [1 ]
Iwama, A
Nishikata, I
Sugiyama, D
Perkins, A
Mucenski, ML
Suda, T
Morishita, K
机构
[1] Keio Univ, Sch Med, Dept Cell Differentiat, Sakaguchi Lab, Tokyo, Japan
[2] Cincinnati Childrens Hosp, Med Ctr, Div Pulm Biol, Cincinnati, OH USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[4] Univ Tokyo, Inst Med Sci, Div Cellular Therapy, Adv Clin Res Ctr, Tokyo, Japan
[5] Miyazaki Univ, Coll Med, Dept Biochem, Miyazaki, Japan
[6] Chiba Univ, Grad Sch Med, Dept Cellular & Mol Biol, Chiba, Japan
关键词
angiopoiesis; Evi1; GATA-2; hematopoiesis;
D O I
10.1038/sj.emboj.7600679
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
The ecotropic viral integration site-1 (Evi1) is an oncogenic transcription factor in murine and human myeloid leukemia. We herein show that Evi1 is predominantly expressed in hematopoietic stem cells (HSCs) in embryos and adult bone marrows, suggesting a physiological role of Evi1 in HSCs. We therefore investigate the role and authentic target genes of Evi1 in hematopoiesis using Evi1(-/-) mice, which die at embryonic day 10.5. HSCs in Evi1(-/-) embryos are markedly decreased in numbers in vivo with defective self-renewing proliferation and repopulating capacity. Notably, expression rate of GATA-2 mRNA, which is essential for proliferation of definitive HSCs, is profoundly reduced in HSCs of Evi1(-/-) embryos. Restoration of the Evi1 or GATA-2 expression in Evi1(-/-) HSCs could prevent the failure of in vitro maintenance and proliferation of HSC through upregulation of GATA-2 expression. An analysis of the GATA-2 promoter region revealed that Evi1 directly binds to GATA-2 promoter as an enhancer. Our results reveal that GATA-2 is presumably one of critical targets for Evi1 and that transcription factors regulate the HSC pool hierarchically.
引用
收藏
页码:1976 / 1987
页数:12
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