Melero J A, Salas M, Salas J
Eur J Biochem. 1976 Aug 16;67(2):341-8. doi: 10.1111/j.1432-1033.1976.tb10697.x.
The synthesis of a classs of proteins with affinity for denatured DNA has been studied in synchronized cultures of the established hamster fibroblast line HIL-1 and its virus-transformed derivative NIL-1-hamster sarcoma virus. It has been found that the synthesis of a DNA-binding protein (P6, molecular weight 50 000) in synchronized untransformed NIL-1 cells follows a pattern different from that observed in the transformed cells. The protein is low in stationary cultures of NIL-1 and NIL-1-hamster sarcoma virus but increases after the cells are stimulated to grow, although the time of maximal P6 synthesis relative to cellular DNA synthesis is different in NIL-1 and NIL-1-hamster sarcoma virus. In contrast, the pattern of synthesis of two other DNA-proteins (P7 and P8') in essentially identical in synchronized untransformed and transformed cells. P7 is very low in resting cultures of both types of cells, but greatly increases early after the cells are stimulated to divide, while P8'is hish in stationary cultures and decreases slightly after the initiation of cellular DNA synthesis has occurred.
在已建立的仓鼠成纤维细胞系HIL-1及其病毒转化衍生物NIL-1-仓鼠肉瘤病毒的同步培养物中,对一类与变性DNA具有亲和力的蛋白质的合成进行了研究。已发现,在同步化的未转化NIL-1细胞中,一种DNA结合蛋白(P6,分子量50000)的合成模式与在转化细胞中观察到的不同。该蛋白在NIL-1和NIL-1-仓鼠肉瘤病毒的静止培养物中含量较低,但在细胞被刺激生长后会增加,尽管相对于细胞DNA合成,P6合成的峰值时间在NIL-1和NIL-1-仓鼠肉瘤病毒中有所不同。相比之下,另外两种DNA结合蛋白(P7和P8')在同步化的未转化细胞和转化细胞中的合成模式基本相同。P7在两种类型细胞的静止培养物中含量都非常低,但在细胞被刺激分裂后早期会大幅增加,而P8'在静止培养物中含量较高,在细胞DNA合成开始后略有下降。