| Literature DB >> 33520997 |
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.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