Lesser J, Lasneret J, Canivet M, Emanoil-Ravier R, Périès J
Virology. 1986 Nov;155(1):249-56. doi: 10.1016/0042-6822(86)90184-4.
5-Azacytidine treatment of Syrian hamster (Mesocricetus auratus) cells, BHK21-cl.13, and primary embryo fibroblasts, activates the production of intracisternal type R particles (IRP) as ascertained by electron microscopy scanning and counting. Efficiency of the activation is dose- and time of treatment-dependent. The transcription of mouse intracisternal A particle (IAP) related sequences, which have been described in Syrian hamster genomic DNA, is increased at the same time. This correlates with demethylation of hamster IAP related genes, as shown by restriction of high molecular weight DNA from 5-azacytidine treated cells with methylation sensitive enzymes, and subsequent electrophoresis and molecular hybridization of the fragments with specific DNA probes. In 5-azacytidine treated cells derived from other hamster species (Cricetulus griseus and C. migratorius), intracisternal R particles were not induced, nor were mouse IAP-related RNAs detected.
用5-氮杂胞苷处理叙利亚仓鼠(金黄地鼠)细胞、BHK21-cl.13细胞和原代胚胎成纤维细胞后,通过电子显微镜扫描和计数确定,激活了池内R型颗粒(IRP)的产生。激活效率取决于处理的剂量和时间。同时,叙利亚仓鼠基因组DNA中已描述的小鼠池内A颗粒(IAP)相关序列的转录增加。这与仓鼠IAP相关基因的去甲基化相关,如用甲基化敏感酶对5-氮杂胞苷处理细胞的高分子量DNA进行酶切,随后对片段进行电泳并用特异性DNA探针进行分子杂交所示。在源自其他仓鼠物种(黑线仓鼠和迁移仓鼠)的5-氮杂胞苷处理细胞中,未诱导出池内R颗粒,也未检测到小鼠IAP相关RNA。