Literature DB >> 33520997

TET-Mediated Epigenetic Regulation in Immune Cell Development and Disease.

Nikolas James Tsiouplis1, David Wesley Bailey1,2,3, Lilly Felicia Chiou4, Fiona Jane Wissink1, Ageliki Tsagaratou1,2,3,4,5,6.   

Abstract

TET proteins oxidize 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further oxidation products in DNA. The oxidized methylcytosines (oxi-mCs) facilitate DNA demethylation and are also novel epigenetic marks. TET loss-of-function is strongly associated with cancer; TET2 loss-of-function mutations are frequently observed in hematological malignancies that are resistant to conventional therapies. Importantly, TET proteins govern cell fate decisions during development of various cell types by activating a cell-specific gene expression program. In this review, we seek to provide a conceptual framework of the mechanisms that fine tune TET activity. Then, we specifically focus on the multifaceted roles of TET proteins in regulating gene expression in immune cell development, function, and disease.
Copyright © 2021 Tsiouplis, Bailey, Chiou, Wissink and Tsagaratou.

Entities:  

Keywords:  5hmC; TET proteins; cancer; epigenetics; immune cell development

Year:  2021        PMID: 33520997      PMCID: PMC7843795          DOI: 10.3389/fcell.2020.623948

Source DB:  PubMed          Journal:  Front Cell Dev Biol        ISSN: 2296-634X


  159 in total

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