Genome-wide Analyses of Transcription Factor GATA3-Mediated Gene Regulation in Distinct T Cell Types

被引:269
作者
Wei, Gang [2 ]
Abraham, Brian J. [2 ]
Yagi, Ryoji [1 ]
Jothi, Raja [3 ]
Cui, Kairong [2 ]
Sharma, Suveena [1 ]
Narlikar, Leelavati [3 ]
Northrup, Daniel L. [2 ]
Tang, Qingsong [2 ]
Paul, William E. [1 ]
Zhu, Jinfang [1 ]
Zhao, Keji [2 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[3] Natl Inst Environm Hlth Sci, Biostat Branch, NIH, Res Triangle Pk, NC 27709 USA
基金
美国国家卫生研究院;
关键词
FACTOR GATA-3; CHROMATIN OCCUPANCY; LINEAGE COMMITMENT; DNA-BINDING; EXPRESSION; DIFFERENTIATION; CD4; FINGER; TH1; IDENTIFICATION;
D O I
10.1016/j.immuni.2011.08.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The transcription factor GATA3 plays an essential role during T cell development and T helper 2 (Th2) cell differentiation. To understand GATA3-mediated gene regulation, we identified genome-wide GATA3 binding sites in ten well-defined developmental and effector T lymphocyte lineages. In the thymus, GATA3 directly regulated many critical factors, including Th-POK, Notch1, and T cell receptor subunits. In the periphery, GATA3 induced a large number of Th2 cell-specific as well as Th2 cell-nonspecific genes, including several transcription factors. Our data also indicate that GATA3 regulates both active and repressive histone modifications of many target genes at their regulatory elements near GATA3 binding sites. Overall, although GATA3 binding exhibited both shared and cell-specific patterns among various T cell lineages, many genes were either positively or negatively regulated by GATA3 in a cell type-specific manner, suggesting that GATA3-mediated gene regulation depends strongly on cofactors existing in different T cells.
引用
收藏
页码:299 / 311
页数:13
相关论文
共 43 条
[1]   Regulation of Th2 differentiation and Il4 locus accessibility [J].
Ansel, K. Mark ;
Djuretic, Ivana ;
Tanasa, Bogdan ;
Rao, Anjana .
ANNUAL REVIEW OF IMMUNOLOGY, 2006, 24 :607-656
[2]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[3]   Erythroid GATA1 function revealed by genome-wide analysis of transcription factor occupancy, histone modifications, and mRNA expression [J].
Cheng, Yong ;
Wu, Weisheng ;
Kumar, Swathi Ashok ;
Yu, Duonan ;
Deng, Wulan ;
Tripic, Tamara ;
King, David C. ;
Chen, Kuan-Bei ;
Zhang, Ying ;
Drautz, Daniela ;
Giardine, Belinda ;
Schuster, Stephan C. ;
Miller, Webb ;
Chiaromonte, Francesca ;
Zhang, Yu ;
Blobel, Gerd A. ;
Weiss, Mitchell J. ;
Hardison, Ross C. .
GENOME RESEARCH, 2009, 19 (12) :2172-2184
[4]   RUNX proteins in transcription factor networks that regulate T-cell lineage choice [J].
Collins, Amelie ;
Littman, Dan R. ;
Taniuchi, Ichiro .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (02) :106-115
[5]   Protein-protein interaction between Fli-1 and GATA-1 mediates synergistic expression of megakaryocyte-specific genes through cooperative DNA binding [J].
Eisbacher, M ;
Holmes, ML ;
Newton, A ;
Hogg, PJ ;
Khachigian, LM ;
Crossley, M ;
Chong, BH .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (10) :3427-3441
[6]   AN ERYTHROCYTE-SPECIFIC DNA-BINDING FACTOR RECOGNIZES A REGULATORY SEQUENCE COMMON TO ALL CHICKEN GLOBIN GENES [J].
EVANS, T ;
REITMAN, M ;
FELSENFELD, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :5976-5980
[7]   Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 bv Polvcomb and HP1 chromodomains [J].
Fischle, W ;
Wang, YM ;
Jacobs, SA ;
Kim, YC ;
Allis, CD ;
Khorasanizadeh, S .
GENES & DEVELOPMENT, 2003, 17 (15) :1870-1881
[8]   Discovering Hematopoietic Mechanisms through Genome-wide Analysis of GATA Factor Chromatin Occupancy [J].
Fujiwara, Tohnu ;
O'Geen, Henriette ;
Keles, Sunduz ;
Blahnik, Kimberly ;
Linnemann, Amelia K. ;
Kang, Yoon-A. ;
Choi, Kyunghee ;
Farnham, Peggy J. ;
Bresnick, Emery H. .
MOLECULAR CELL, 2009, 36 (04) :667-681
[9]   Identification and Characterization of Enhancers Controlling the Inflammatory Gene Expression Program in Macrophages [J].
Ghisletti, Serena ;
Barozzi, Iros ;
Mietton, Fiore ;
Polletti, Sara ;
De Santa, Francesca ;
Venturini, Elisa ;
Gregory, Lorna ;
Lonie, Lorne ;
Chew, Adeline ;
Wei, Chia-Lin ;
Ragoussis, Jiannis ;
Natoli, Gioacchino .
IMMUNITY, 2010, 32 (03) :317-328
[10]   A distal conserved sequence element controls Ifng gene expression by T cells and NK cells [J].
Hatton, Robin D. ;
Harrington, Laurie E. ;
Luther, Rita J. ;
Wakefield, Therese ;
Janowski, Karen M. ;
Oliver, James R. ;
Lallone, Roger L. ;
Murphy, Kenneth M. ;
Weaver, Casey T. .
IMMUNITY, 2006, 25 (05) :717-729