A Systematic Approach to Identify Candidate Transcription Factors that Control Cell Identity

被引:119
作者
D'Alessio, Ana C. [1 ]
Fan, Zi Peng [1 ,2 ]
Wert, Katherine J. [1 ]
Baranov, Petr [3 ]
Cohen, Malkiel A. [1 ]
Saini, Janmeet S. [4 ,5 ]
Cohick, Evan [1 ]
Charniga, Carol [4 ]
Dadon, Daniel [1 ,6 ]
Hannett, Nancy M. [1 ]
Young, Michael J. [3 ]
Temple, Sally [4 ]
Jaenisch, Rudolf [1 ,6 ]
Lee, Tong Ihn [1 ]
Young, Richard A. [1 ,6 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Computat & Syst Biol Program, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Med, Massachusetts Eye & Ear, Schepens Eye Res Inst, Boston, MA 02114 USA
[4] Neural Stem Cell Inst, Rensselaer, NY 12144 USA
[5] SUNY Albany, Dept Biomed Sci, Albany, NY 12201 USA
[6] MIT, Dept Biol, Cambridge, MA 02139 USA
来源
STEM CELL REPORTS | 2015年 / 5卷 / 05期
关键词
RETINAL-PIGMENT EPITHELIUM; PLURIPOTENT STEM-CELLS; DEFINED FACTORS; DIRECT CONVERSION; SUPER-ENHANCERS; REGULATORY DNA; FIBROBLASTS; DISEASE; EXPRESSION; FATE;
D O I
10.1016/j.stemcr.2015.09.016
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Hundreds of transcription factors (TFs) are expressed in each cell type, but cell identity can be induced through the activity of just a small number of core TFs. Systematic identification of these core TFs for a wide variety of cell types is currently lacking and would establish a foundation for understanding the transcriptional control of cell identity in development, disease, and cell-based therapy. Here, we describe a computational approach that generates an atlas of candidate core TFs for a broad spectrum of human cells. The potential impact of the atlas was demonstrated via cellular reprogramming efforts where candidate core TFs proved capable of converting human fibroblasts to retinal pigment epithelial-like cells. These results suggest that candidate core TFs from the atlas will prove a useful starting point for studying transcriptional control of cell identity and reprogramming in many human cell types.
引用
收藏
页码:763 / 775
页数:13
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