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10.1111/imr.12213

http://scihub22266oqcxt.onion/10.1111/imr.12213
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suck abstract from ncbi


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pmid25319330
      Immunol+Rev 2014 ; 262 (1 ): 96-112
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  • Epigenomics of macrophages #MMPMID25319330
  • Gosselin D ; Glass CK
  • Immunol Rev 2014[Nov]; 262 (1 ): 96-112 PMID25319330 show ga
  • Macrophages play essential roles in tissue homeostasis, pathogen elimination, and tissue repair. A defining characteristic of these cells is their ability to efficiently adapt to a variety of abruptly changing and complex environments. This ability is intrinsically linked to a capacity to quickly alter their transcriptome, and this is tightly associated with the epigenomic organization of these cells and, in particular, their enhancer repertoire. Indeed, enhancers are genomic sites that serve as platforms for the integration of signaling pathways with the mechanisms that regulate mRNA transcription. Notably, transcription is pervasive at active enhancers and enhancer RNAs (eRNAs) are tightly coupled to regulated transcription of protein-coding genes. Furthermore, given that each cell type possesses a defining enhancer repertoire, studies on enhancers provide a powerful method to study how specialization of functions among the diverse macrophage subtypes may arise. Here, we review recent studies providing insights into the distinct mechanisms that contribute to the establishment of enhancers and their role in the regulation of transcription in macrophages.
  • |*Epigenesis, Genetic [MESH]
  • |*Epigenomics [MESH]
  • |*Gene Expression Regulation [MESH]
  • |Animals [MESH]
  • |Cell Lineage [MESH]
  • |Enhancer Elements, Genetic [MESH]
  • |Humans [MESH]
  • |Macrophages/immunology/*metabolism [MESH]
  • |Nucleosomes/metabolism [MESH]
  • |Open Reading Frames/genetics [MESH]
  • |Organ Specificity [MESH]
  • |RNA Interference [MESH]
  • |RNA, Untranslated/genetics [MESH]
  • |Signal Transduction [MESH]
  • |Transcription Factors/metabolism [MESH]


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