Fukunaga R, Matsuyama M, Okamura H, Nagata K, Nagata S, Sokawa Y
Nucleic Acids Res. 1986 Jun 11;14(11):4421-36. doi: 10.1093/nar/14.11.4421.
The relative levels of DNA methylation at CCGG sequences within and around the interferon-gamma (IFN-gamma) gene in normal human tissues and cell lines were examined by Southern blot analysis using isoschizomeric restriction enzymes, HpaII and MspI. On the test of normal tissues, the IFN-gamma gene was undermethylated only in a small population of T lymphocyte, whereas the gene was fully methylated in T cell-depleted lymphocytes and uterus cells. In TCL-Fuj cell line which is a T cell line producing a high level of IFN-gamma spontaneously, the IFN-gamma gene was undermethylated. Moreover, the extent of DNA methylation was inversely correlated to the level of expression of the IFN-gamma gene in several T cell lines including sublines derived from TCL-Fuj cells. However, partial or complete unmethylation at the CCGG sites of IFN-gamma gene was observed in a promyelocytic leukemia cell line and two epithelial cell lines that fail to produce IFN-gamma irrespective of induction. These results suggest that undermethylation of IFN-gamma gene is necessary but not sufficient for its efficient expression.
利用同裂酶HpaII和MspI,通过Southern印迹分析检测了正常人组织和细胞系中干扰素-γ(IFN-γ)基因及其周围CCGG序列的DNA甲基化相对水平。在正常组织检测中,IFN-γ基因仅在一小部分T淋巴细胞中低甲基化,而在T细胞耗竭的淋巴细胞和子宫细胞中该基因完全甲基化。在自发产生高水平IFN-γ的T细胞系TCL-Fuj细胞系中,IFN-γ基因低甲基化。此外,在包括源自TCL-Fuj细胞的亚系在内的多个T细胞系中,DNA甲基化程度与IFN-γ基因的表达水平呈负相关。然而,在一个早幼粒细胞白血病细胞系和两个无论是否诱导均不产生IFN-γ的上皮细胞系中,观察到IFN-γ基因的CCGG位点部分或完全未甲基化。这些结果表明,IFN-γ基因的低甲基化对于其有效表达是必要的,但不是充分的。