Falk L, Lindahl T, Klein G
IARC Sci Publ (1971). 1978(24 Pt 1):131-5.
Baboon lymphoblastoid cell lines (LCL) transformed with herpesvirus papio were evaluated for the state of HVP DNA in the cells by caesium chloride density-gradient centrifugation and DNA-cRNA filter hybridization. Five HVP producer cultures and one non-producer culture were studied and non-integrated and integrated HVP DNA were detected in all producer cultures whereas only integrated HVP DNA could be demonstrated in the non-producer LCL. Non-integrated HVP dna had a density of 1.715--1.716 g/cm3 in caesium chloride corresponding to a guanine + cytosine content of 56--57%.
通过氯化铯密度梯度离心和DNA-cRNA滤膜杂交,对用狒狒疱疹病毒转化的狒狒淋巴母细胞系(LCL)中的HVP DNA状态进行了评估。研究了5种HVP产生细胞培养物和1种非产生细胞培养物,在所有产生细胞培养物中均检测到非整合和整合的HVP DNA,而在非产生LCL中仅能证明存在整合的HVP DNA。在氯化铯中,非整合的HVP dna密度为1.715--1.716 g/cm3,对应鸟嘌呤+胞嘧啶含量为56--57%。