Gopalan Sunita, Kasza Aneta, Xu Weili, Kiss Daniel L, Wilczynska Katarzyna M, Rydel Russell E, Kordula Tomasz
Department of Biochemistry, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
J Neurochem. 2005 Aug;94(3):763-73. doi: 10.1111/j.1471-4159.2005.03204.x. Epub 2005 Jun 22.
The distal serpin subcluster contains genes encoding alpha1-antichymotrypsin (ACT), protein C inhibitor (PCI), kallistatin (KAL) and the KAL-like protein, which are expressed in hepatocytes, but only the act gene is expressed in astrocytes. We show here that the tissue-specific expression of these genes associates with astrocyte- and hepatocyte-specific chromatin structures. In hepatocytes, we identified 12 Dnase I-hypersensitive sites (DHSs) that were distributed throughout the entire subcluster, with the promoters of expressed genes accessible to restriction enzyme digestion. In astrocytes, only six DHSs were located exclusively in the 5' flanking region of the act gene, with its promoter also accessible to restriction enzyme digestion. The acetylation of histone H3 and H4 was found throughout the subcluster in both cell types but this acetylation did not correlate with the expression pattern of these serpin genes. Analysis of histone modifications at the promoters of the act and pci genes revealed that methylation of histone H3 on lysine 4 correlated with their expression pattern in both cell types. In addition, inhibition of methyltransferase activity resulted in suppression of ACT and PCI mRNA expression. We propose that lysine 4 methylation of histone H3 correlates with the tissue-specific expression pattern of these serpin genes.
远端丝氨酸蛋白酶抑制剂亚簇包含编码α1-抗糜蛋白酶(ACT)、蛋白C抑制剂(PCI)、血管抑素(KAL)和KAL样蛋白的基因,这些基因在肝细胞中表达,但只有act基因在星形胶质细胞中表达。我们在此表明,这些基因的组织特异性表达与星形胶质细胞和肝细胞特异性染色质结构相关。在肝细胞中,我们鉴定出12个分布于整个亚簇的脱氧核糖核酸酶I超敏位点(DHSs),表达基因的启动子可被限制酶消化。在星形胶质细胞中,只有6个DHSs仅位于act基因的5'侧翼区域,其启动子也可被限制酶消化。在两种细胞类型中,整个亚簇均发现组蛋白H3和H4的乙酰化,但这种乙酰化与这些丝氨酸蛋白酶抑制剂基因的表达模式无关。对act和pci基因启动子处组蛋白修饰的分析表明,组蛋白H3赖氨酸4位的甲基化与它们在两种细胞类型中的表达模式相关。此外,甲基转移酶活性的抑制导致ACT和PCI mRNA表达的抑制。我们提出,组蛋白H3赖氨酸4位甲基化与这些丝氨酸蛋白酶抑制剂基因的组织特异性表达模式相关。