Gambari R, Barbieri R, Piva R, Tecce R, Fisher P B, Giacomini P, Natali P G
Istituto di Chimica Biologica, Università di Ferrara, Italy.
Ann N Y Acad Sci. 1987;511:292-307. doi: 10.1111/j.1749-6632.1987.tb36258.x.
The control of expression of human class II MHC genes has been studied in lymphoid and melanoma cells. Specific unmethylation of all restriction sites nearby the promoter regions has been detected in all cell lines and tissues studied, irrespective of their ability to express class II MHC products. The main functional role of DNA methylation appears, on the contrary, to be the regulation of a fraction of the nucleotide polymorphism of class II MHC genes. Constitutive expression of these genes can be modified by recombinant IFN-gamma and by the demethylating agent 5-azacytidine. Both the modifiers differentially regulate the levels of class II MHC and invariant chain products. In melanoma cells IFN-gamma derepresses transcription of a 1.2-Kb HLA-DR alpha mRNA, but does not affect the levels of a 0.8-Kb HLA-DR alpha specific mRNA. These molecular changes are triggered by IFN-gamma through a protein-synthesis-dependent pathway.
人类Ⅱ类主要组织相容性复合体(MHC)基因表达的调控已在淋巴细胞和黑色素瘤细胞中展开研究。在所研究的所有细胞系和组织中,均检测到启动子区域附近所有限制性酶切位点的特异性去甲基化,无论它们表达Ⅱ类MHC产物的能力如何。相反,DNA甲基化的主要功能作用似乎是对Ⅱ类MHC基因一部分核苷酸多态性的调控。这些基因的组成型表达可通过重组干扰素-γ和去甲基化剂5-氮杂胞苷进行修饰。两种修饰剂对Ⅱ类MHC和恒定链产物的水平有不同的调节作用。在黑色素瘤细胞中,干扰素-γ可解除对1.2kb HLA-DRα mRNA转录的抑制,但不影响0.8kb HLA-DRα特异性mRNA的水平。这些分子变化是由干扰素-γ通过蛋白质合成依赖性途径触发的。