Discovering Hematopoietic Mechanisms through Genome-wide Analysis of GATA Factor Chromatin Occupancy

被引:306
作者
Fujiwara, Tohnu [1 ]
O'Geen, Henriette [4 ]
Keles, Sunduz [2 ,3 ]
Blahnik, Kimberly [4 ]
Linnemann, Amelia K. [1 ]
Kang, Yoon-A. [1 ]
Choi, Kyunghee [5 ]
Farnham, Peggy J. [4 ]
Bresnick, Emery H. [1 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Inst Med Res, Madison, WI 53705 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Stat, Madison, WI 53706 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI 53706 USA
[4] Univ Calif Davis, Genome Ctr, Davis, CA 95616 USA
[5] Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO 63110 USA
关键词
TRANSCRIPTION FACTOR GATA-1; ERYTHROID GENE-EXPRESSION; DNA-BINDING; CELL-PROLIFERATION; DOMAIN ACTIVATION; MICE LACKING; FACTOR SCL; C-KIT; PROTEIN; LEUKEMIA;
D O I
10.1016/j.molcel.2009.11.001
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
GATA factors interact with simple DNA motifs (WGATAR) to regulate critical processes, including hematopoiesis, but very few WGATAR motifs are occupied in genomes. Given the rudimentary knowledge of mechanisms underlying this restriction and how GATA factors establish genetic networks, we used ChIP-seq to define GATA-1 and GATA-2 occupancy genome-wide in erythroid cells. Coupled with genetic complementation analysis and transcriptional profiling, these studies revealed a rich collection of targets containing a characteristic binding motif of greater complexity than WGATAR. GATA factors occupied loci encoding multiple components of the ScI/TAL1 complex, a master regulator of hematopoiesis and leukemogenic target. Mechanistic analyses provided evidence for cross-regulatory and autoregulatory interactions among components of this complex, including GATA-2 induction of the hematopoietic corepressor ETO-2 and an ETO-2-negative autoregulatory loop. These results establish fundamental principles underlying GATA factor mechanisms in chromatin and illustrate a complex network of considerable importance for the control of hematopoiesis.
引用
收藏
页码:667 / 681
页数:15
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