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Chromatin activity identifies differential gene regulation across human ancestries

View ORCID ProfileKade P. Pettie, View ORCID ProfileMaxwell Mumbach, View ORCID ProfileAmanda J. Lea, View ORCID ProfileJulien Ayroles, View ORCID ProfileHoward Y. Chang, View ORCID ProfileMaya Kasowski, View ORCID ProfileHunter B. Fraser
doi: https://doi.org/10.1101/2022.11.25.517959
Kade P. Pettie
1Department of Biology, Stanford University, Stanford, CA
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Maxwell Mumbach
2Department of Genetics, Stanford University, Stanford, CA
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Amanda J. Lea
3Department of Biological Sciences, Vanderbilt University, Nashville, TN
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Julien Ayroles
4Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ
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Howard Y. Chang
5Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA
6Howard Hughes Medical Institute, Stanford University, Stanford, CA
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Maya Kasowski
7Sean N. Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, CA
8Department of Pathology, Stanford University School of Medicine, Stanford, CA
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Hunter B. Fraser
1Department of Biology, Stanford University, Stanford, CA
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  • For correspondence: hbfraser@stanford.edu
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Abstract

Current evidence suggests that cis-regulatory elements controlling gene expression may be the predominant target of natural selection in humans and other species. Detecting selection acting on these elements is critical to understanding evolution but remains challenging because we do not know which mutations will affect gene regulation. To address this, we devised an approach to search for lineage-specific selection on chromatin activity, transcription factor binding, and chromosomal looping—critical steps in transcriptional regulation. Applying this approach to lymphoblastoid cells from 831 individuals of either European or African descent, we find strong signals of differential chromatin activity linked to gene expression differences between ancestries in numerous contexts, but no evidence of functional differences in chromosomal looping. Moreover, we show that enhancers rather than promoters display the strongest signs of selection associated with sites of differential transcription factor binding. Overall, our study indicates that some cis-regulatory adaptation may be more easily detected at the level of chromatin than DNA sequence. This work provides a vast resource of genomic interaction data from diverse human populations and establishes a novel selection test that will benefit future study of regulatory evolution in humans and other species.

Competing Interest Statement

The authors have declared no competing interest.

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 November 25, 2022.
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Chromatin activity identifies differential gene regulation across human ancestries
Kade P. Pettie, Maxwell Mumbach, Amanda J. Lea, Julien Ayroles, Howard Y. Chang, Maya Kasowski, Hunter B. Fraser
bioRxiv 2022.11.25.517959; doi: https://doi.org/10.1101/2022.11.25.517959
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Chromatin activity identifies differential gene regulation across human ancestries
Kade P. Pettie, Maxwell Mumbach, Amanda J. Lea, Julien Ayroles, Howard Y. Chang, Maya Kasowski, Hunter B. Fraser
bioRxiv 2022.11.25.517959; doi: https://doi.org/10.1101/2022.11.25.517959

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