Beug H, Hayman M J, Graf T, Benedict S H, Wallbank A M, Vogt P K
Virology. 1985 Aug;145(1):141-53. doi: 10.1016/0042-6822(85)90209-0.
The avian leukemia sarcoma virus S13 transforms chicken and Japanese quail embryo fibroblasts and chicken erythroid cells in tissue culture. S13-induced erythroid transformation requires culture conditions suitable for the growth of normal erythroid precursors (H. Beug and M. J. Hayman (1984), Cell 36, 963-972). S13-transformed erythroid colonies contain a high percentage of cells that differentiate in absence of erythropoietin. S13 is defective in pol and env functions but can code for a complete set of gag proteins. Nonproducer cell clones transformed by S13 release a noninfectious viral particle containing gag but no functional env or pol proteins. They also synthesize a transformation-specific protein of 155,000 molecular weight. This protein reacts with antibody to viral envelope glycoproteins and appears to represent onc as well as env sequences. The 155,000-molecular weight env-linked protein does not cross react immunologically with an antiserum against the v-erb A and v-erb B gene products.
禽白血病肉瘤病毒S13可在组织培养中转化鸡和日本鹌鹑胚胎成纤维细胞以及鸡红细胞。S13诱导的红细胞转化需要适合正常红细胞前体生长的培养条件(H. 贝格和M. J. 海曼(1984年),《细胞》36卷,963 - 972页)。S13转化的红细胞集落包含高比例的在无促红细胞生成素情况下分化的细胞。S13在pol和env功能方面存在缺陷,但能编码一套完整的gag蛋白。由S13转化的非生产性细胞克隆释放出一种不含功能性env或pol蛋白但含有gag的非感染性病毒颗粒。它们还合成一种分子量为155,000的转化特异性蛋白。该蛋白与病毒包膜糖蛋白抗体发生反应,似乎代表了癌基因以及env序列。这种分子量为155,000的与env相关的蛋白与抗v-erb A和v-erb B基因产物的抗血清没有免疫交叉反应。