| Literature DB >> 34935162 |
Atsushi Onodera1,2, Masahiro Kiuchi1, Kota Kokubo1, Toshinori Nakayama1,3.
Abstract
Epigenetic regulation of gene transcription in the immune system is important for proper control of protective and pathogenic inflammation. Aberrant epigenetic modifications are often associated with dysregulation of the immune cells, including lymphocytes and macrophages, leading to pathogenic inflammation and autoimmune diseases. Two classical epigenetic markers-histone modifications and DNA cytosine methylation, the latter is the 5 position of the cytosine base in the context of CpG dinucleotides-play multiple roles in the immune system. CxxC domain-containing proteins, which basically bind to the non-methylated CpG (i.e., epigenetic "readers"), often function as "writers" of the epigenetic markers via their catalytic domain within the proteins or by interacting with other epigenetic modifiers. We herein report the most recent advances in our understanding of the functions of CxxC domain-containing proteins in the immune system and inflammation, mainly focusing on T cells and macrophages.Entities:
Keywords: DNA methylation; helper T cells; ten-eleven translocation (TET) proteins; trithorax
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Year: 2021 PMID: 34935162 DOI: 10.1111/imr.13056
Source DB: PubMed Journal: Immunol Rev ISSN: 0105-2896 Impact factor: 12.988