| Literature DB >> 30686579 |
Hideyuki Yoshida1, Caleb A Lareau2, Ricardo N Ramirez3, Samuel A Rose4, Barbara Maier4, Aleksandra Wroblewska4, Fiona Desland4, Aleksey Chudnovskiy4, Arthur Mortha4, Claudia Dominguez5, Julie Tellier6, Edy Kim7, Dan Dwyer7, Susan Shinton8, Tsukasa Nabekura9, YiLin Qi10, Bingfei Yu11, Michelle Robinette12, Ki-Wook Kim12, Amy Wagers13, Andrew Rhoads3, Stephen L Nutt6, Brian D Brown4, Sara Mostafavi14, Jason D Buenrostro15, Christophe Benoist16.
Abstract
A complete chart of cis-regulatory elements and their dynamic activity is necessary to understand the transcriptional basis of differentiation and function of an organ system. We generated matched epigenome and transcriptome measurements in 86 primary cell types that span the mouse immune system and its differentiation cascades. This breadth of data enable variance components analysis that suggests that genes fall into two distinct classes, controlled by either enhancer- or promoter-driven logic, and multiple regression that connects genes to the enhancers that regulate them. Relating transcription factor (TF) expression to the genome-wide accessibility of their binding motifs classifies them as predominantly openers or closers of local chromatin accessibility, pinpointing specific cis-regulatory elements where binding of given TFs is likely functionally relevant, validated by chromatin immunoprecipitation sequencing (ChIP-seq). Overall, this cis-regulatory atlas provides a trove of information on transcriptional regulation through immune differentiation and a foundational scaffold to define key regulatory events throughout the immunological genome.Entities:
Keywords: ATAC-seq; Transcriptional regulation; chromatin; enhancer; epigenomics; immune cell differentiation; transcription factor
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Year: 2019 PMID: 30686579 PMCID: PMC6785993 DOI: 10.1016/j.cell.2018.12.036
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582