Friend of GATA-1-independent transcriptional repression: a novel mode of GATA-1 function

被引:54
作者
Johnson, Kirby D.
Boyer, Meghan E.
Kang, Jeong-Ah
Wickrema, Amittha
Cantor, Alan B.
Bresnick, Emery H. [1 ]
机构
[1] Univ Wisconsin, Sch Med, Dept Pharmacol, Madison, WI 53706 USA
[2] Univ Chicago, Hematol Oncol Sect, Chicago, IL 60637 USA
[3] Childrens Hosp, Div Pediat Hematol Oncol, Boston, MA 02115 USA
关键词
D O I
10.1182/blood-2007-02-072983
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The GATA-1 -interacting protein Friend Of GATA-1 (FOG-1) is essential for the proper transcriptional activation and repression of numerous GATA-1 target genes. Although FOG-1 -independent activation by GATA-1 has been described, all known examples of GATA-1-mediated repression are FOG-1 dependent. In the GATA-1-null G1E cell line, estrogen receptor ligand binding domain (ER) chimeras of either wild-type GATA-1 or a FOG-1-binding defective mutant of GATA-1 repressed several genes similarly upon activation with P-estradiol. Repression also occurred in a FOG-1-null cell line expressing ER-GATA-1 and during ex vivo erythropoiesis. At the Lyl1 and Rgs18 loci, we found highly restricted occupancy by GATA-1 and GATA-2, indicating that these genes are direct targets of GATA factor regulation. The identification of genes repressed by GATA-1 independent of FOG-1 defines a novel mode of GATA-1-mediated transcriptional regulation.
引用
收藏
页码:5230 / 5233
页数:4
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