Human Gene-Centered Transcription Factor Networks for Enhancers and Disease Variants

被引:83
作者
Bass, Juan I. Fuxman [1 ,2 ]
Sahni, Nidhi [3 ,4 ]
Shrestha, Shaleen [1 ,2 ]
Garcia-Gonzalez, Aurian [1 ,2 ]
Mori, Akihiro [1 ,2 ]
Bhat, Numana [1 ,2 ]
Yi, Song [3 ,4 ]
Hill, David E. [3 ,4 ]
Vidal, Marc [3 ,4 ]
Walhout, Albertha J. M. [1 ,2 ,3 ]
机构
[1] Univ Massachusetts, Sch Med, Program Syst Biol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[3] Dana Farber Canc Inst, Dept Canc Biol, Ctr Canc Syst Biol CCSB, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
ONE-HYBRID ASSAYS; REGULATORY NETWORK; PROTEIN-DNA; LHX4; GENE; MUTATIONS; PROMOTER; BINDING; MOUSE;
D O I
10.1016/j.cell.2015.03.003
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
Gene regulatory networks (GRNs) comprising interactions between transcription factors (TFs) and regulatory loci control development and physiology. Numerous disease-associated mutations have been identified, the vast majority residing in non-coding regions of the genome. As current GRN mapping methods test one TF at a time and require the use of cells harboring the mutation(s) of interest, they are not suitable to identify TFs that bind to wildtype and mutant loci. Here, we use gene-centered yeast one-hybrid (eY1H) assays to interrogate binding of 1,086 human TFs to 246 enhancers, as well as to 109 non-coding disease mutations. We detect both loss and gain of TF interactions with mutant loci that are concordant with target gene expression changes. This work establishes eY1H assays as a powerful addition to the toolkit of mapping human GRNs and for the high-throughput characterization of genomic variants that are rapidly being identified by genome-wide association studies.
引用
收藏
页码:661 / 673
页数:13
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