Widespread evidence of cooperative DNA binding by transcription factors in Drosophila development

被引:64
|
作者
Kazemian, Majid [1 ,2 ,3 ]
Pham, Hannah [4 ]
Wolfe, Scot A. [4 ,5 ]
Brodsky, Michael H. [4 ,6 ]
Sinha, Saurabh [1 ,7 ]
机构
[1] Univ Illinois, Dept Comp Sci, Urbana, IL USA
[2] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD USA
[3] NHLBI, Ctr Immunol, NIH, Bethesda, MD USA
[4] Univ Massachusetts, Program Gene Funct & Express, Sch Med, Amherst, MA 01003 USA
[5] Univ Massachusetts, Dept Biochem & Mol Pharmacol, Sch Med, Amherst, MA 01003 USA
[6] Univ Massachusetts, Dept Mol Med, Sch Med, Amherst, MA 01003 USA
[7] Univ Illinois, Inst Genom Biol, Urbana, IL USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PROTEIN-INTERACTION MAP; COLLABORATIVE COMPETITION; REGULATORY CODE; GLOBAL ANALYSIS; PARTNER CODE; GAGA FACTOR; CHROMATIN; SPECIFICITY; NETWORK; ORGANIZATION;
D O I
10.1093/nar/gkt598
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
Regulation of eukaryotic gene transcription is often combinatorial in nature, with multiple transcription factors (TFs) regulating common target genes, often through direct or indirect mutual interactions. Many individual examples of cooperative binding by directly interacting TFs have been identified, but it remains unclear how pervasive this mechanism is during animal development. Cooperative TF binding should be manifest in genomic sequences as biased arrangements of TF-binding sites. Here, we explore the extent and diversity of such arrangements related to gene regulation during Drosophila embryogenesis. We used the DNA-binding specificities of 322 TFs along with chromatin accessibility information to identify enriched spacing and orientation patterns of TF-binding site pairs. We developed a new statistical approach for this task, specifically designed to accurately assess inter-site spacing biases while accounting for the phenomenon of homotypic site clustering commonly observed in developmental regulatory regions. We observed a large number of short-range distance preferences between TF-binding site pairs, including examples where the preference depends on the relative orientation of the binding sites. To test whether these binding site patterns reflect physical interactions between the corresponding TFs, we analyzed 27 TF pairs whose binding sites exhibited short distance preferences. In vitro protein-protein binding experiments revealed that > 65% of these TF pairs can directly interact with each other. For five pairs, we further demonstrate that they bind cooperatively to DNA if both sites are present with the preferred spacing. This study demonstrates how DNA-binding motifs can be used to produce a comprehensive map of sequence signatures for different mechanisms of combinatorial TF action.
引用
收藏
页码:8237 / 8252
页数:16
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