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Published TCIMAIL newest issue No.197
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Histone lysine methylation plays important roles in the organization of chromatin domains and the regulation of gene expression. Among histone lysine methyltransferases (HKMTs) in mammals, G9a and G9a like protein (GLP) are the primary enzymes for mono- and dimethylation at Lys 9 of histone H3 (H3K9me1 and H3K9me2, respectively) and exist for the most part as a G9a–GLP heteromeric complex.1)
BIX 01294 (1) inhibits H3K9 methylation by GLP, G9a HKMTs,2,3) and H3K36 methylation by oncoproteins4) (Table). The inhibition is caused by binding of 1 to the substrate peptide groove of GLP.3) 1 can improve the reprogramming efficiency of mouse embryonic fibroblasts or fetal neural progenitor cells to induced pluripotent stem cells without using c-Myc and SOX2.5,6)
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