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Temporal analysis suggests a reciprocal relationship between 3D chromatin structure and transcription

View ORCID ProfileKathleen S. M. Reed, View ORCID ProfileEric S. Davis, View ORCID ProfileMarielle L. Bond, Alan Cabrera, Eliza Thulson, View ORCID ProfileI. Yoseli Quiroga, Shannon Cassel, Kamisha T. Woolery, View ORCID ProfileIsaac Hilton, View ORCID ProfileHyejung Won, Michael I. Love, View ORCID ProfileDouglas H. Phanstiel
doi: https://doi.org/10.1101/2022.05.05.490836
Kathleen S. M. Reed
2Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA
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  • ORCID record for Kathleen S. M. Reed
Eric S. Davis
3Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599, USA
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Marielle L. Bond
2Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA
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Alan Cabrera
4Department of Bioengineering, Rice University, Houston, TX 77005, USA
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Eliza Thulson
2Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA
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I. Yoseli Quiroga
5Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC 27599, USA
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Shannon Cassel
5Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC 27599, USA
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Kamisha T. Woolery
5Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC 27599, USA
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Isaac Hilton
4Department of Bioengineering, Rice University, Houston, TX 77005, USA
6Department of Biosciences, Rice University, Houston, TX 77005, USA
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Hyejung Won
7Department of Genetics and Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, USA
8Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, USA
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Michael I. Love
9Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA
10Department of Biostatistics, University of North Carolina, Chapel Hill, Chapel Hill, NC 27599, USA
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Douglas H. Phanstiel
2Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA
3Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599, USA
5Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC 27599, USA
11Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA
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  • For correspondence: douglas_phanstiel@med.unc.edu
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SUMMARY

To infer potential causal relationships between 3D chromatin structure, enhancers, and gene transcription, we mapped each feature in a genome-wide fashion across eight narrowly-spaced timepoints of macrophage activation. Enhancers and genes connected by loops exhibited stronger correlations between histone H3K27 acetylation and expression than can be explained by genomic distance or physical proximity alone. Changes in acetylation at looped distal enhancers preceded changes in gene expression. Changes in gene expression exhibit a directional bias at differential loop anchors; gained loops are associated with increased expression of genes oriented away from the center of the loop, while lost loops were often accompanied by high levels of transcription with the loop boundaries themselves. Taken together, these results are consistent with a reciprocal relationship in which loops can facilitate increased transcription by connecting promoters to distal enhancers while high levels of transcription can impede loop formation.

HIGHLIGHTS

  • LPS + IFNγ triggers genome-wide changes in chromatin looping, enhancer acetylation, and gene expression

  • Looped enhancer-promoter pairs exhibit ordered and correlated changes in acetylation and expression

  • Changes in gene expression exhibit a directional bias at differential loop anchors

  • Lost loops are associated with high levels of transcription within loop boundaries

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE201376

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 05, 2022.
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Temporal analysis suggests a reciprocal relationship between 3D chromatin structure and transcription
Kathleen S. M. Reed, Eric S. Davis, Marielle L. Bond, Alan Cabrera, Eliza Thulson, I. Yoseli Quiroga, Shannon Cassel, Kamisha T. Woolery, Isaac Hilton, Hyejung Won, Michael I. Love, Douglas H. Phanstiel
bioRxiv 2022.05.05.490836; doi: https://doi.org/10.1101/2022.05.05.490836
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Temporal analysis suggests a reciprocal relationship between 3D chromatin structure and transcription
Kathleen S. M. Reed, Eric S. Davis, Marielle L. Bond, Alan Cabrera, Eliza Thulson, I. Yoseli Quiroga, Shannon Cassel, Kamisha T. Woolery, Isaac Hilton, Hyejung Won, Michael I. Love, Douglas H. Phanstiel
bioRxiv 2022.05.05.490836; doi: https://doi.org/10.1101/2022.05.05.490836

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