两种牛白血病病毒产生细胞系的不同反激活过程

H J Wagner, P Blankenstein, A Bondzio, H Burkhardt
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引用次数: 0

摘要

采用酶免疫法(EIA)对牛白血病病毒(BLV) FLC/BLV 44及其FLC/BLV 44-4亚系进行了为期6个多月的定量比较研究,采用抗gp51和p24的单克隆抗体。FLC/BLV 44对gp51(2 ~ 6因子)和p24(2因子)的合成明显高于FLC/BLV 44-4。在BLV-LTR (pBLV β - Gal质粒)的转录控制下,通过β -半乳糖苷酶指示器官的转移来确定两系的转激活状态。瞬时实验表明,FLC/BLV 44的β -半乳糖苷酶活性明显高于亚系FLC/BLV 44-4。在这两种细胞系中,BLV抗原合成强度与反活化过程明显密切相关。
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[Different transactivation processes in two bovine leukemia virus producing cell lines].

Comparative studies were conducted through more than six months into quantitative of bovine leukaemia virus (BLV) antigen of FLC/BLV 44 and its FLC/BLV 44-4 subline by means of an enzyme immuno-assay (EIA), using monoclonal antibodies against gp51 and p24. Synthesis of gp51 (factors of two to six) and of p24 (factor of two) by FLC/BLV 44 was clearly higher than that by FLC/BLV 44-4. The transactivation status in either line was determined by transfer of the beta-galactosidase indicator organ under transcription control of BLV-LTR (in pBLV beta Gal plasmid). Transient experiments showed beta-galactosidase activity in the FLC/BLV 44 to be clearly higher than that in subline FLC/BLV 44-4. There is obviously in both cell lines a close correlation between intensity of BLV antigen synthesis and transactivation processes.

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