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Evidence for additive and synergistic action of mammalian enhancers during cell fate determination
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 bindi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004103/ https://www.ncbi.nlm.nih.gov/pubmed/33770473 http://dx.doi.org/10.7554/eLife.65381 |
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author | Choi, Jinmi Lysakovskaia, Kseniia Stik, Gregoire Demel, Carina Söding, Johannes Tian, Tian V Graf, Thomas Cramer, Patrick |
author_facet | Choi, Jinmi Lysakovskaia, Kseniia Stik, Gregoire Demel, Carina Söding, Johannes Tian, Tian V Graf, Thomas Cramer, Patrick |
author_sort | Choi, Jinmi |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8004103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80041032021-03-31 Evidence for additive and synergistic action of mammalian enhancers during cell fate determination Choi, Jinmi Lysakovskaia, Kseniia Stik, Gregoire Demel, Carina Söding, Johannes Tian, Tian V Graf, Thomas Cramer, Patrick eLife Computational and Systems Biology 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. eLife Sciences Publications, Ltd 2021-03-26 /pmc/articles/PMC8004103/ /pubmed/33770473 http://dx.doi.org/10.7554/eLife.65381 Text en © 2021, Choi et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Choi, Jinmi Lysakovskaia, Kseniia Stik, Gregoire Demel, Carina Söding, Johannes Tian, Tian V Graf, Thomas Cramer, Patrick Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title | Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title_full | Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title_fullStr | Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title_full_unstemmed | Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title_short | Evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
title_sort | evidence for additive and synergistic action of mammalian enhancers during cell fate determination |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004103/ https://www.ncbi.nlm.nih.gov/pubmed/33770473 http://dx.doi.org/10.7554/eLife.65381 |
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