Sequence-specific transcription factors (TFs) regulate gene expression through their interactions with DNA sequences in the genome. The overarching goal of this project is to continue developing approaches and data sets for understanding the DNA binding specificities of TFs, and to understand the effects of coding polymorphisms with TFs' DNA binding domains on their DNA binding preferences. Identification of TFs'DNA binding specificities is important in understanding transcriptional regulatory networks, in particular in the prediction of cis regulatory modules, inference of cis regulatory codes, and interpretation of in vivo TF binding data and gene expression data. Identification of the DNA binding effects of such polymorphic TF variants will be essential in studies aimed at understanding the gene regulatory effects resulting from natural genetic variation. This project will focus on human TFs associated with diseases, in particular Crohn's disease, ulcerative colitis, diabetes, autism and other neuropsychiatric disorders. Our results will provide data that will likely be of importance to other systems, and more generally, our data, approaches, technologies, and database will be useful not only for human TFs but also for model organism studies. Specifically, we will: (1) develop systematic approaches for extracting fine-level features of TFs'DNA binding specificity when comparing very similar proteins;(2) generate clone resources and proteins for ~200 total human proteins (reference and polymorphic variants) with disease/trait associations;(3) determine the DNA binding specificities of the ~200 total reference and polymorphic TFs, and identify the effects of coding polymorphisms within TFs on their DNA binding specificities;(4) develop high- throughput, array-based technology for determining the effects of CpG DNA methylation on TF-DNA binding;(5) maintain the UniPROBE database that hosts high-resolution, universal protein binding microarray data on TFs'DNA binding specificities.

Public Health Relevance

This project is focused on better understanding the DNA binding specificities of regulatory transcription factors. In this project, we will transcription factors corresponding to the reference genome, and also those containing polymorphisms that may affect their DNA binding specificities. The findings from this project will provide data on the potential effects of transcription factor polymorphisms on gene regulation.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
2R01HG003985-04
Application #
7788367
Study Section
Special Emphasis Panel (ZRG1-GGG-F (02))
Program Officer
Pazin, Michael J
Project Start
2006-07-26
Project End
2013-05-31
Budget Start
2010-09-01
Budget End
2011-05-31
Support Year
4
Fiscal Year
2010
Total Cost
$600,000
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
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Hafner, Antonina; Stewart-Ornstein, Jacob; Purvis, Jeremy E et al. (2017) p53 pulses lead to distinct patterns of gene expression albeit similar DNA-binding dynamics. Nat Struct Mol Biol 24:840-847
Inukai, Sachi; Kock, Kian Hong; Bulyk, Martha L (2017) Transcription factor-DNA binding: beyond binding site motifs. Curr Opin Genet Dev 43:110-119
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Hume, Maxwell A; Barrera, Luis A; Gisselbrecht, Stephen S et al. (2015) UniPROBE, update 2015: new tools and content for the online database of protein-binding microarray data on protein-DNA interactions. Nucleic Acids Res 43:D117-22
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Christodoulou, Danos C; Wakimoto, Hiroko; Onoue, Kenji et al. (2014) 5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy. J Clin Invest 124:1364-70

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