| Literature DB >> 29706550 |
Peggie Cheung1, Francesco Vallania2, Hayley C Warsinske2, Michele Donato2, Steven Schaffert2, Sarah E Chang1, Mai Dvorak1, Cornelia L Dekker3, Mark M Davis4, Paul J Utz5, Purvesh Khatri6, Alex J Kuo7.
Abstract
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.Entities:
Keywords: Epigenetics; aging; cell identity; chromatin modifications; heritability; histones; immune system; mass cytometry; transcriptional noise; twins
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Year: 2018 PMID: 29706550 PMCID: PMC5984186 DOI: 10.1016/j.cell.2018.03.079
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582