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The cis-Regulatory Atlas of the Mouse Immune System
Author(s) -
Hideyuki Yoshida,
Caleb A. Lareau,
Ricardo N. Ramírez,
Samuel A. Rose,
Bárbara Maier,
Aleksandra Wroblewska,
Fiona Desland,
Aleksey Chudnovskiy,
Arthur Mortha,
Claudia X. Dominguez,
Julie Tellier,
Edy Y. Kim,
Dan Dwyer,
Susan A. Shinton,
Tsukasa Nabekura,
Yilin Qi,
Bingfei Yu,
Michelle L. Robinette,
Ki-Wook Kim,
Amy J. Wagers,
Andrew Rhoads,
Stephen L. Nutt,
Brian D. Brown,
Sara Mostafavi,
Jason D. Buenrostro,
Christophe Benoist
Publication year - 2019
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.2018.12.036
Subject(s) - biology , enhancer , epigenome , chromatin , chromatin immunoprecipitation , transcription factor , computational biology , genetics , regulatory sequence , gene , regulation of gene expression , transcriptome , promoter , gene expression , dna methylation
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.

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