Clarke M F, Trainor C D, Mann D L, Gallo R C, Reitz M S
Virology. 1984 May;135(1):97-104. doi: 10.1016/0042-6822(84)90120-x.
Leukemic peripheral blood lymphocytes from individuals infected with the human T-cell leukemia/lymphoma virus (HTLV) were found to express little or no viral RNA before being put into tissue culture. Within 24-48 hr, viral RNA expression increased at least four- to eightfold. Established HTLV-infected cell lines constitutively express viral RNA. Southern blots of DNA from HTLV-infected cells digested with the methylation-sensitive restriction enzyme HpaII showed that the proviral DNA was methylated in all of the uncultured peripheral blood cells tested. In contrast, no proviral methylation was detected in any of the cell lines examined, suggesting a functional correlation between methylation and viral RNA expression. However, DNA from HTLV-infected lymphocytes cultured for 48 hr (by which time increases in viral RNA expression are evident) did not differ detectably with respect to proviral DNA methylation from uncultured cells, suggesting that the increase in viral RNA expression after short-term culture is mediated by mechanisms independent of changes in DNA methylation.
在感染人类T细胞白血病/淋巴瘤病毒(HTLV)的个体的白血病外周血淋巴细胞被置于组织培养之前,发现其几乎不表达或不表达病毒RNA。在24 - 48小时内,病毒RNA表达至少增加了4至8倍。已建立的HTLV感染细胞系组成性地表达病毒RNA。用甲基化敏感限制性酶HpaII消化HTLV感染细胞的DNA进行Southern印迹分析表明,在所测试的所有未培养外周血细胞中,前病毒DNA是甲基化的。相比之下,在所检查的任何细胞系中均未检测到前病毒甲基化,这表明甲基化与病毒RNA表达之间存在功能相关性。然而,培养48小时的HTLV感染淋巴细胞(此时病毒RNA表达增加明显)的DNA在前病毒DNA甲基化方面与未培养细胞没有可检测到的差异,这表明短期培养后病毒RNA表达的增加是由独立于DNA甲基化变化的机制介导的。