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


ABSTRACT: 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.

SUBMITTER: Rhie SK 

PROVIDER: S-EPMC6292713 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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

Rhie Suhn K SK   Schreiner Shannon S   Witt Heather H   Armoskus Chris C   Lay Fides D FD   Camarena Adrian A   Spitsyna Valeria N VN   Guo Yu Y   Berman Benjamin P BP   Evgrafov Oleg V OV   Knowles James A JA   Farnham Peggy J PJ  

Science advances 20181213 12


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 v  ...[more]

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