Animal Transcription Networks as Highly Connected, Quantitative Continua

被引:243
作者
Biggin, Mark D. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Genom Div, Berkeley, CA 94720 USA
关键词
INTERACTIONS IN-VIVO; FACTOR-BINDING-SITES; HEAT-SHOCK FACTOR; DNA-BINDING; GENE-EXPRESSION; CHROMATIN ACCESSIBILITY; GLUCOCORTICOID-RECEPTOR; PROTEIN-BINDING; FUNCTIONAL ELEMENTS; ESTROGEN-RECEPTOR;
D O I
10.1016/j.devcel.2011.09.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To understand how transcription factors function, it is essential to determine the range of genes that they each bind and regulate in vivo. Here I review evidence that most animal transcription factors each bind to a majority of genes over a quantitative series of DNA occupancy levels. These continua span functional, quasifunctional, and nonfunctional DNA binding events. Factor regulatory specificities are distinguished by quantitative differences in DNA occupancy patterns. I contrast these results with models for transcription networks that define discrete sets of direct target and nontarget genes and consequently do not fully capture the complexity observed in vivo.
引用
收藏
页码:611 / 626
页数:16
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