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. 2020 Nov 7;12:169. doi: 10.1186/s13148-020-00962-x

Fig. 1.

Fig. 1

Epigenetics alteration and mechanism in PTCL. MLL2:MLL2 can activate the transcription of genes by methylating histone H3 at the 4th lysine (H3K4me).EZH2:EZH2 inhibits gene expression by catalysing trimethylation of lysine 27 of histone H3 (H3K27m3).HDAC : HATs catalyse the transfer of an acetyl group from acetyl- CoA to the NH2 group of lysine residues of histone H3 and histone H4 while HDACs remove it. DNMTs: DNMTs catalyse the transfer of methyl groups to cytosine nucleotides of CpG island DNA.TET2: encodes TET which converts 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC). When TET2 is mutated, there is a pathogenic decrease in 5hmC leading to suppression of gene transcription.IDH2: Mutations of IDH2, such as gain-of-function R140 and R172 substitutions, lead to toxic 2-hydroxyglutarate (2HG) accumulate; which inhibits TET and decreases the levels of 5hmC. TET: ten eleven translocation protein; 2HG: 2-hydroxyglutarate; IDH2:isocitrate dehydrogenase 2; 5hmC: 5-hydroxymethylcytosine; EZH2: enhancer of zeste 2; K27me3: trimethylation at lysine 27 of histone 3 (H3K27me3); K4me3: trimethylation at lysine 4 of histone 3 (H3K4me3)