Bogovskii B P, Lezhneva O M
Biull Eksp Biol Med. 1978 Mar;85(3):334-7.
Murine endogenous oncornavirus (C-type) genome expression was investigated in methylcholanthrene-induced (MC-induced) tumours of low-leukemic CC57BR mice by means of the radioimmunodiffusion method, using the precipitating test-systems. The gs-1 antigen of murine C-type viral p30 protein and Gross leukemia virus type-specific antigen (AGLV) served as viral genome markers. The gs-1 antigen was found in the primary and continuous MC-induced sarcomas, whereas AGLV appeared only during the tumour passage. A distinct association was revealed between the quantity of p30 protein (gs-1 antigen titre) and the presence of AGLV. Simultaneously with the appearance of AGLV the gs-1 titre increased markedly and the AGLV disappearance was always accompanied by a decrease of the gs-1 titre. The data presented suggest a coordinated expression of the two investigated proteins of murine C-type endogenous oncornaviruses in the chemically-induced tumours of CC57BR mice.
利用沉淀检测系统,通过放射免疫扩散法,对低白血病CC57BR小鼠甲基胆蒽诱导(MC诱导)肿瘤中的鼠内源性肿瘤病毒(C型)基因组表达进行了研究。鼠C型病毒p30蛋白的gs-1抗原和格罗斯白血病病毒型特异性抗原(AGLV)用作病毒基因组标记。在原发性和连续性MC诱导的肉瘤中发现了gs-1抗原,而AGLV仅在肿瘤传代过程中出现。p30蛋白量(gs-1抗原滴度)与AGLV的存在之间存在明显关联。与AGLV出现同时,gs-1滴度显著增加,而AGLV消失时总是伴随着gs-1滴度下降。所呈现的数据表明,在CC57BR小鼠化学诱导肿瘤中,鼠C型内源性肿瘤病毒的两种研究蛋白存在协同表达。