Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10758879 | Biochemical and Biophysical Research Communications | 2013 | 5 Pages |
Abstract
We recently demonstrated that metallothionein (MT)-1 A is a direct target gene negatively regulated by PU.1. In this study, we revealed that the expression of PU.1 was increased and accompanied by downregulation of MT-1A expression during TPA-induced THP-1 monocyte differentiation. Chromatin immunoprecipitation (ChIP) analysis demonstrated that PU.1 and the methyl CpG binding protein (MeCP) 2 bound to the same â887 to â602 region in the MT-1A promoter, and the binding of these proteins to this promoter was enhanced during differentiation. Consistently, bisulfite sequencing analyses around this region revealed that the proportion of methylated CpG sites was obivously increased during differentiation. In addition, ChIP analysis demonstrated that acetylated histone H4 around this region tended to be reduced and this may also play a role in the reduction of MT-1A expression during differentiation. Taken together, these findings suggest that MT-1A is epigenetically regulated by PU.1 during monocytic differentiation.
Keywords
12-O-tetradecanoylphorbol-13-acetateAMLPU.1HSCsDnmtHDACGAPDHtPADMSODNA methyltransferaseROSHistone modificationchromatin immunoprecipitationMonocyte differentiationDimethyl sulfoxidehematopoietic stem cellsacute myeloid leukemiaMetallothioneinDNA methylationEpigenetic regulationhistone deacetylaseCHiPglyceraldehyde 3-phosphate dehydrogenaseReactive oxygen species
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Authors
Sawami Suzuki, Hiroko Nakano, Shinichiro Takahashi,