Human Immune Cell Epigenomic Signatures in Response to Infectious Diseases and Chemical Exposures.

Wenliang Wang, Manoj Hariharan,Anna Bartlett, Cesar Barragan, Rosa Castanon, Vince Rothenberg, Haili Song,Joseph Nery, Andrew Aldridge,Jordan Altshul, Mia Kenworthy,Wubin Ding, Hanqing Liu, Wei Tian,Jingtian Zhou, Huaming Chen,Bei Wei, Irem B Gündüz, Todd Norell, Timothy J Broderick,Micah T McClain, Lisa L Satterwhite,Thomas W Burke,Elizabeth A Petzold, Xiling Shen,Christopher W Woods, Vance G Fowler,Felicia Ruffin, Parinya Panuwet,Dana B Barr, Jennifer L Beare, Anthony K Smith, Rachel R Spurbeck,Sindhu Vangeti, Irene Ramos,German Nudelman, Stuart C Sealfon, Flora Castellino, Anna Maria Walley, Thomas Evans,Fabian Müller, William J Greenleaf,Joseph R Ecker

bioRxiv : the preprint server for biology(2023)

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摘要
Variations in DNA methylation patterns in human tissues have been linked to various environmental exposures and infections. Here, we identified the DNA methylation signatures associated with multiple exposures in nine major immune cell types derived from peripheral blood mononuclear cells (PBMCs) at single-cell resolution. We performed methylome sequencing on 111,180 immune cells obtained from 112 individuals who were exposed to different viruses, bacteria, or chemicals. Our analysis revealed 790,662 differentially methylated regions (DMRs) associated with these exposures, which are mostly individual CpG sites. Additionally, we integrated methylation and ATAC-seq data from same samples and found strong correlations between the two modalities. However, the epigenomic remodeling in these two modalities are complementary. Finally, we identified the minimum set of DMRs that can predict exposures. Overall, our study provides the first comprehensive dataset of single immune cell methylation profiles, along with unique methylation biomarkers for various biological and chemical exposures.
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