The role and regulation of friend of GATA-1 (FOG-1) during blood development in the zebrafish

被引:34
作者
Amigo, Julio D. [1 ,2 ]
Ackermann, Gabriele E. [1 ]
Cope, John J. [1 ]
Yu, Ming [3 ]
Cooney, Jeffrey D. [1 ]
Ma, Dongdong [1 ]
Langer, Nathaniel B. [1 ]
Shafizadeh, Ebrahim [1 ]
Shaw, George C. [1 ]
Horsely, Wyatt [3 ]
Trede, Nikolaus S. [2 ,3 ,4 ]
Davidson, Alan J. [2 ,3 ]
Barut, Bruce A. [3 ]
Zhou, Yi [2 ,3 ]
Wojiski, Sarah A. [1 ,2 ]
Traver, David [3 ]
Moran, Tyler B. [3 ]
Kourkoulis, George [4 ]
Hsu, Karl [4 ]
Kanki, John P. [2 ,4 ]
Shah, Dhvanit I. [1 ]
Lin, Hui Feng [1 ]
Handin, Robert I. [1 ,2 ]
Cantor, Alan B. [2 ,3 ,4 ]
Paw, Barry H. [1 ,2 ,3 ,4 ]
机构
[1] Brigham & Womens Hosp, Div Hematol, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR GATA-1; MAST-CELL LINEAGE; TRANSGENIC ZEBRAFISH; T-CELL; GENE; EXPRESSION; FATE; PU.1; ERYTHROPOIESIS; ANTAGONISM;
D O I
10.1182/blood-2008-12-189910
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The nuclear protein FOG-1 binds transcription factor GATA-1 to facilitate erythroid and megakaryocytic maturation. However, little is known about the function of FOG-1 during myeloid and lymphoid development or how FOG-1 expression is regulated in any tissue. We used in situ hybridization, gain- and loss-of-function studies in zebrafish to address these problems. Zebrafish FOG-1 is expressed in early hematopoietic cells, as well as heart, viscera, and paraspinal neurons, suggesting that it has multifaceted functions in organogenesis. We found that FOG-1 is dispensable for endoderm specification but is required for endoderm patterning affecting the expression of late-stage T-cell markers, independent of GATA-1. The suppression of FOG-1, in the presence of normal GATA-1 levels, induces severe anemia and thrombocytopenia and expands myeloid-progenitor cells, indicating that FOG-1 is required during erythroid/myeloid commitment. To functionally interrogate whether GATA-1 regulates FOG-1 in vivo, we used bioinformatics combined with transgenic assays. Thus, we identified 2 cis-regulatory elements that control the tissue-specific gene expression of FOG-1. One of these enhancers contains functional GATA-binding sites, indicating the potential for a regulatory loop in which GATA factors control the expression of their partner protein FOG-1. ( Blood. 2009; 114: 4654-4663)
引用
收藏
页码:4654 / 4663
页数:10
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