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Single-Cell Chromatin Modification Profiling Reveals Increased Epigenetic Variations with Aging
Author(s) -
Peggie Cheung,
Francesco Vallania,
Hayley Warsinske,
Michele Donato,
Steven Schaffert,
Sarah E. Chang,
Mai Dvorak,
Cornelia L. Dekker,
Mark M. Davis,
Paul J. Utz,
Purvesh Khatri,
Alex Kuo
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.03.079
Subject(s) - chromatin , biology , epigenetics , mass cytometry , histone , histone modifying enzymes , bivalent chromatin , chromatin remodeling , microbiology and biotechnology , dna methylation , epigenomics , genetics , computational biology , dna , phenotype , gene expression , gene
Post-translational modifications of histone proteins and exchanges of histone variants of chromatin are central to the regulation of nearly all DNA-templated biological processes. However, the degree and variability of chromatin modifications in specific human immune cells remain largely unknown. Here, we employ a highly multiplexed mass cytometry analysis to profile the global levels of a broad array of chromatin modifications in primary human immune cells at the single-cell level. Our data reveal markedly different cell-type- and hematopoietic-lineage-specific chromatin modification patterns. Differential analysis between younger and older adults shows that aging is associated with increased heterogeneity between individuals and elevated cell-to-cell variability in chromatin modifications. Analysis of a twin cohort unveils heritability of chromatin modifications and demonstrates that aging-related chromatin alterations are predominantly driven by non-heritable influences. Together, we present a powerful platform for chromatin and immunology research. Our discoveries highlight the profound impacts of aging on chromatin modifications.

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