Division of Molecular Hematology, Kitasato University Graduate School of Medical Sciences, Miniami-ku, Sagamihara, Kanagawa, Japan.
Biochem Biophys Res Commun. 2013 Apr 12;433(3):349-53. doi: 10.1016/j.bbrc.2013.03.007. Epub 2013 Mar 15.
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 -887 to -602 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.
我们最近证实,金属硫蛋白(MT)-1A 是一个受 PU.1 负调控的直接靶基因。在这项研究中,我们揭示了在 TPA 诱导的 THP-1 单核细胞分化过程中,PU.1 的表达增加,并伴随着 MT-1A 表达的下调。染色质免疫沉淀(ChIP)分析表明,PU.1 和甲基化 CpG 结合蛋白(MeCP)2 结合到 MT-1A 启动子的相同 -887 至 -602 区域,并且在分化过程中这些蛋白与该启动子的结合增强。一致地,围绕该区域的亚硫酸氢盐测序分析表明,在分化过程中,甲基化 CpG 位点的比例明显增加。此外,ChIP 分析表明,该区域周围乙酰化组蛋白 H4 趋于减少,这在分化过程中 MT-1A 表达的减少中也可能起作用。综上所述,这些发现表明,在单核细胞分化过程中,MT-1A 受 PU.1 的表观遗传调控。