Environment Drives Selection and Function of Enhancers Controlling Tissue-Specific Macrophage Identities
Author(s) -
David Gosselin,
Verena M. Link,
Casey E. Romanoski,
Gregory J. Fonseca,
Dawn Z. Eichenfield,
Nathanael J. Spann,
Joshua D. Stender,
Hyun Bae Chun,
Hannah Garner,
Frédéric Geissmann,
Christopher K. Glass
Publication year - 2014
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.2014.11.023
Subject(s) - biology , enhancer , selection (genetic algorithm) , function (biology) , microbiology and biotechnology , macrophage , computational biology , genetics , transcription factor , gene , in vitro , artificial intelligence , computer science
Macrophages reside in essentially all tissues of the body and play key roles in innate and adaptive immune responses. Distinct populations of tissue macrophages also acquire context-specific functions that are important for normal tissue homeostasis. To investigate mechanisms responsible for tissue-specific functions, we analyzed the transcriptomes and enhancer landscapes of brain microglia and resident macrophages of the peritoneal cavity. In addition, we exploited natural genetic variation as a genome-wide "mutagenesis" strategy to identify DNA recognition motifs for transcription factors that promote common or subset-specific binding of the macrophage lineage-determining factor PU.1. We find that distinct tissue environments drive divergent programs of gene expression by differentially activating a common enhancer repertoire and by inducing the expression of divergent secondary transcription factors that collaborate with PU.1 to establish tissue-specific enhancers. These findings provide insights into molecular mechanisms by which tissue environment influences macrophage phenotypes that are likely to be broadly applicable to other cell types.
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