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Global landscape of mouse and human cytokine transcriptional regulation
Author(s) -
Sebastian Carrasco Pro,
Alvaro Dafonte Imedio,
Clarissa Stephanie Santoso,
Kok Ann Gan,
Jared Allan Sewell,
Melissa Martinez,
Rebecca Sereda,
Shivani Mehta,
Juan I. Fuxman Bass
Publication year - 2018
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gky787
Subject(s) - biology , cytokine , transcription factor , computational biology , transcriptional regulation , gene regulatory network , immune system , regulation of gene expression , gene , phenotype , genetics , microbiology and biotechnology , gene expression
Cytokines are cell-to-cell signaling proteins that play a central role in immune development, pathogen responses, and diseases. Cytokines are highly regulated at the transcriptional level by combinations of transcription factors (TFs) that recruit cofactors and the transcriptional machinery. Here, we mined through three decades of studies to generate a comprehensive database, CytReg, reporting 843 and 647 interactions between TFs and cytokine genes, in human and mouse respectively. By integrating CytReg with other functional datasets, we determined general principles governing the transcriptional regulation of cytokine genes. In particular, we show a correlation between TF connectivity and immune phenotype and disease, we discuss the balance between tissue-specific and pathogen-activated TFs regulating each cytokine gene, and cooperativity and plasticity in cytokine regulation. We also illustrate the use of our database as a blueprint to predict TF-disease associations and identify potential TF-cytokine regulatory axes in autoimmune diseases. Finally, we discuss research biases in cytokine regulation studies, and use CytReg to predict novel interactions based on co-expression and motif analyses which we further validated experimentally. Overall, this resource provides a framework for the rational design of future cytokine gene regulation studies.

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