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. 2017 Jan 3;9(1):2. doi: 10.3390/cancers9010002

Table 1.

Mutations/rearrangements of histone writers and erasers in B-cell progenitor acute lymphoblastic leukemia (BCP-ALL).

Gene (Reference) Histone-Modifying Function Frequency of Mutations/Rearrangements in BCP-ALL Subgroups Enriched
CREBBP [50,51,53,55,57] H3K18 acetyltransferase (and other H3/H4 residues) Rare in cases without hyperdiploidy and relapse Relapse, hyperdiploidy
EP300 [50,55] H3K18 acetyltransferase (and other H3/H4 residues) <1% -
MLL1 [3,5,6,82,122,123] H3K4 methyltransferase 5% -
NSD2 [44,91] H3K36 methyltransferase Not documented in unselected patients, up to 14% in subgroups ETV6-RUNX1-rearranged
SETD2 [44,60,93,124] H3K36 methyltransferase 12% MLL- and ETV6-RUNX1- rearrangements, relapse
EZH2 [44,55,94] H3K4 methyltransferase 1.3% hypodiploidy
JAK2 [99,100,125,126] H3Y41 phosphorylase Not determined in unselected patients, up to 10% in high risk disease BCR-ABL1-like, Down syndrome, high-risk disease