Gergely L, Sternås L, Dillner J, Klein G
Intervirology. 1984;22(2):85-96. doi: 10.1159/000149538.
The size classes of the Epstein-Barr virus(EBV)-induced nuclear antigen (EB-NA) have been determined in EBV-carrying sublines of two originally EBV-negative Burkitt lymphomas, converted in vitro by two different EBV substrains, and in somatic hybrids between two EBV-carrying cell lines or between an EBV-positive and an EBV-negative line. Partially purified EBNA components were detected by Western blotting and subsequent exposure to antiserum/alkaline-phosphatase-coupled protein A complexes. Converted Ramos and BJAB sublines contained the main EBNA components characteristic for the virus donor strain. The EBNA components of the Ramos and BJAB cells converted by P3HR-1 virus were similar to each other and to the components of the P3HR-1 donor cell, whereas the EBNA of the cells converted by B95-8 virus resembled the B95-8 donor line. It was concluded that the size variation of EBNA is determined by the viral genome. The parental lines of the somatic hybrids studied (Raji, P3HR-1, Namalwa and Daudi) contained EBNA components of different molecular weight (MW) classes. The higher MW forms ranged from 70K to 80K. Several distinctive lower MW components also were present. The somatic hybrids expressed the main EBNA components of both parental lines. Hybrids between EBV-carrying and EBV-genome-negative lines contained the characteristic EBNA component of the EBV-positive parent. It was concluded that the size variation of EBNA is under strict genetic control which prevails in the hybrids in a codominant fashion.
在两种原本EB病毒阴性的伯基特淋巴瘤的携带EB病毒亚系中,已确定了EB病毒(EBV)诱导的核抗原(EB-NA)的大小类别。这两种亚系是通过两种不同的EBV亚菌株在体外转化而来的,此外还研究了两个携带EBV的细胞系之间或一个EBV阳性与一个EBV阴性细胞系之间的体细胞杂种。通过蛋白质印迹法并随后用抗血清/碱性磷酸酶偶联的蛋白A复合物进行检测,来检测部分纯化的EBNA成分。转化后的拉莫斯(Ramos)和BJAB亚系含有病毒供体菌株特有的主要EBNA成分。由P3HR-1病毒转化的拉莫斯和BJAB细胞的EBNA成分彼此相似,且与P3HR-1供体细胞的成分相似,而由B95-8病毒转化的细胞的EBNA则类似于B95-8供体系。得出的结论是,EBNA的大小变异由病毒基因组决定。所研究的体细胞杂种的亲代细胞系(拉吉(Raji)、P3HR-1、纳马尔瓦(Namalwa)和道迪(Daudi))含有不同分子量(MW)类别的EBNA成分。较高分子量的形式范围为70K至80K。还存在几种独特的较低分子量成分。体细胞杂种表达了两个亲代细胞系的主要EBNA成分。携带EBV与EBV基因组阴性细胞系之间的杂种含有EBV阳性亲代细胞特有的EBNA成分。得出的结论是,EBNA的大小变异受到严格的遗传控制,这种控制在杂种中以共显性方式占主导地位。