H4K20me3
H4K20 trimethylation has a role in gene silencing and indexing of pericentric heterochromatin (PMID: 15145825). Loss of this mark on a global level in the genome is a hallmark of human cancer (PMID: 15765097).
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Modified variants | Histone H4 |
---|---|
Writer/s | Histone-lysine N-methyltransferase SUV420H1, Histone-lysine N-methyltransferase SUV420H2, Probable histone-lysine N-methyltransferase NSD2 |
Eraser/s | |
Disease associations | Blood disorder: Beta-thalassemia, Sickle cell disease (SCD); PMID: 20495075 Cancer: All; PMID: 15765097 Neurological disorders: Fragile X syndrome; PMID: 20843831 Neurological disorders: Sotos syndrome; PMID: 20018718 |
Sites of lysine methylation H1K186me1, H1K25me1, H2BK5me1, H3K27me1, H3K27me2, H3K27me3, H3K36me1, H3K36me2, H3K36me3, H3K4me1, H3K4me2, H3K4me3, H3K79me1, H3K79me2, H3K79me3, H3K9me1, H3K9me2, H3K9me3, H4K20me1, H4K20me2, H4K20me3