Dynamic trans-acting factor colocalization in human cells.

Dan Xie, Alan P Boyle, Linfeng Wu, Jie Zhai, Trupti Kawli, Michael Snyder
Author Information
  1. Dan Xie: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.

Abstract

Different trans-acting factors (TFs) collaborate and act in concert at distinct loci to perform accurate regulation of their target genes. To date, the cobinding of TF pairs has been investigated in a limited context both in terms of the number of factors within a cell type and across cell types and the extent of combinatorial colocalizations. Here, we use an approach to analyze TF colocalization within a cell type and across multiple cell lines at an unprecedented level. We extend this approach with large-scale mass spectrometry analysis of immunoprecipitations of 50 TFs. Our combined approach reveals large numbers of interesting TF-TF associations. We observe extensive change in TF colocalizations both within a cell type exposed to different conditions and across multiple cell types. We show distinct functional annotations and properties of different TF cobinding patterns and provide insights into the complex regulatory landscape of the cell.

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Grants

  1. U54HG004558/NHGRI NIH HHS
  2. K99 HG007356/NHGRI NIH HHS
  3. U01 HG003156/NHGRI NIH HHS
  4. U01 HL107393/NHLBI NIH HHS
  5. U54HG006996/NHGRI NIH HHS
  6. U54 HG006996/NHGRI NIH HHS
  7. U54 HG004558/NHGRI NIH HHS

MeSH Term

Artificial Intelligence
Binding Sites
Cell Line
Chromatin Immunoprecipitation
Gene Regulatory Networks
Humans
Regulatory Sequences, Nucleic Acid
Sequence Analysis, DNA
Transcription Factors

Chemicals

Transcription Factors

Word Cloud

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