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Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation

As part of PsychENCODE, we developed a three-dimensional (3D) epigenomic map of primary cultured neuronal cells derived from olfactory neuroepithelium (CNON). We mapped topologically associating domains and high-resolution chromatin interactions using Hi-C and identified regulatory elements using ch...

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Autores principales: Rhie, Suhn K., Schreiner, Shannon, Witt, Heather, Armoskus, Chris, Lay, Fides D., Camarena, Adrian, Spitsyna, Valeria N., Guo, Yu, Berman, Benjamin P., Evgrafov, Oleg V., Knowles, James A., Farnham, Peggy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292713/
https://www.ncbi.nlm.nih.gov/pubmed/30555922
http://dx.doi.org/10.1126/sciadv.aav8550
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author Rhie, Suhn K.
Schreiner, Shannon
Witt, Heather
Armoskus, Chris
Lay, Fides D.
Camarena, Adrian
Spitsyna, Valeria N.
Guo, Yu
Berman, Benjamin P.
Evgrafov, Oleg V.
Knowles, James A.
Farnham, Peggy J.
author_facet Rhie, Suhn K.
Schreiner, Shannon
Witt, Heather
Armoskus, Chris
Lay, Fides D.
Camarena, Adrian
Spitsyna, Valeria N.
Guo, Yu
Berman, Benjamin P.
Evgrafov, Oleg V.
Knowles, James A.
Farnham, Peggy J.
author_sort Rhie, Suhn K.
collection PubMed
description As part of PsychENCODE, we developed a three-dimensional (3D) epigenomic map of primary cultured neuronal cells derived from olfactory neuroepithelium (CNON). We mapped topologically associating domains and high-resolution chromatin interactions using Hi-C and identified regulatory elements using chromatin immunoprecipitation and nucleosome positioning assays. Using epigenomic datasets from biopsies of 63 living individuals, we found that epigenetic marks at distal regulatory elements are more variable than marks at proximal regulatory elements. By integrating genotype and metadata, we identified enhancers that have different levels corresponding to differences in genetic variation, gender, smoking, and schizophrenia. Motif searches revealed that many CNON enhancers are bound by neuronal-related transcription factors. Last, we combined 3D epigenomic maps and gene expression profiles to predict enhancer-target gene interactions on a genome-wide scale. This study not only provides a framework for understanding individual epigenetic variation using a primary cell model system but also contributes valuable data resources for epigenomic studies of neuronal epithelium.
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spelling pubmed-62927132018-12-14 Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation Rhie, Suhn K. Schreiner, Shannon Witt, Heather Armoskus, Chris Lay, Fides D. Camarena, Adrian Spitsyna, Valeria N. Guo, Yu Berman, Benjamin P. Evgrafov, Oleg V. Knowles, James A. Farnham, Peggy J. Sci Adv Research Articles As part of PsychENCODE, we developed a three-dimensional (3D) epigenomic map of primary cultured neuronal cells derived from olfactory neuroepithelium (CNON). We mapped topologically associating domains and high-resolution chromatin interactions using Hi-C and identified regulatory elements using chromatin immunoprecipitation and nucleosome positioning assays. Using epigenomic datasets from biopsies of 63 living individuals, we found that epigenetic marks at distal regulatory elements are more variable than marks at proximal regulatory elements. By integrating genotype and metadata, we identified enhancers that have different levels corresponding to differences in genetic variation, gender, smoking, and schizophrenia. Motif searches revealed that many CNON enhancers are bound by neuronal-related transcription factors. Last, we combined 3D epigenomic maps and gene expression profiles to predict enhancer-target gene interactions on a genome-wide scale. This study not only provides a framework for understanding individual epigenetic variation using a primary cell model system but also contributes valuable data resources for epigenomic studies of neuronal epithelium. American Association for the Advancement of Science 2018-12-13 /pmc/articles/PMC6292713/ /pubmed/30555922 http://dx.doi.org/10.1126/sciadv.aav8550 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Rhie, Suhn K.
Schreiner, Shannon
Witt, Heather
Armoskus, Chris
Lay, Fides D.
Camarena, Adrian
Spitsyna, Valeria N.
Guo, Yu
Berman, Benjamin P.
Evgrafov, Oleg V.
Knowles, James A.
Farnham, Peggy J.
Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title_full Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title_fullStr Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title_full_unstemmed Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title_short Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
title_sort using 3d epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292713/
https://www.ncbi.nlm.nih.gov/pubmed/30555922
http://dx.doi.org/10.1126/sciadv.aav8550
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