Evidence for additive and synergistic action of mammalian enhancers during cell fate determination

Author:

Choi Jinmi1ORCID,Lysakovskaia Kseniia1ORCID,Stik Gregoire2ORCID,Demel Carina1,Söding Johannes3ORCID,Tian Tian V2ORCID,Graf Thomas2ORCID,Cramer Patrick1ORCID

Affiliation:

1. Max Planck Institute for Biophysical Chemistry, Department of Molecular Biology, Göttingen, Germany

2. Gene Regulation, Stem Cells and Cancer Program, Centre for Genomic Regulation (CRG), Barcelona, Spain

3. Max Planck Institute for Biophysical Chemistry, Quantitative Biology and Bioinformatics, Göttingen, Germany

Abstract

Enhancer activity drives cell differentiation and cell fate determination, but it remains unclear how enhancers cooperate during these processes. Here we investigate enhancer cooperation during transdifferentiation of human leukemia B-cells to macrophages. Putative enhancers are established by binding of the pioneer factor C/EBPα followed by chromatin opening and enhancer RNA (eRNA) synthesis from H3K4-monomethylated regions. Using eRNA synthesis as a proxy for enhancer activity, we find that most putative enhancers cooperate in an additive way to regulate transcription of assigned target genes. However, transcription from 136 target genes depends exponentially on the summed activity of its putative paired enhancers, indicating that these enhancers cooperate synergistically. The target genes are cell type-specific, suggesting that enhancer synergy can contribute to cell fate determination. Enhancer synergy appears to depend on cell type-specific transcription factors, and such interacting enhancers are not predicted from occupancy or accessibility data that are used to detect superenhancers.

Funder

Max-Planck-Gesellschaft

Deutsche Forschungsgemeinschaft

European Research Council

Volkswagen Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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