Gallagher B M, Hartig W J
In Vitro. 1976 Mar;12(3):165-72. doi: 10.1007/BF02796438.
The utilization of [3H]-5-uridine by CP-1268 cells was studied. Uridine was rapidly transported into these cells by a concentration dependent, saturable process. Exogenous uridine rapidly equilibrated with cellular nucleotide pools and virtually all of the uridine transported into the cells was phosphorylated. Uridine incorporation into RNA was studied by continuous and pulse-labeling techniques in the prescence or absence of actinomycin D and cordycepin. These studies have shown that the pattern of unstable RNA precursor and relatively stable RNA product relationship known to exist in mammalian cells similarly exists in insect cells in vitro. This pattern varied markedly with pulse-labeling time and required the addition of RNA inhibitors to block reincorporation of intracellular labeled metabolites during the chase.
研究了CP - 1268细胞对[3H] - 5 - 尿苷的利用情况。尿苷通过浓度依赖性的饱和过程迅速转运到这些细胞中。外源性尿苷迅速与细胞核苷酸池达到平衡,并且几乎所有转运到细胞内的尿苷都被磷酸化。在有或没有放线菌素D和冬虫夏草素的情况下,通过连续和脉冲标记技术研究了尿苷掺入RNA的情况。这些研究表明,已知存在于哺乳动物细胞中的不稳定RNA前体和相对稳定RNA产物关系模式在体外昆虫细胞中同样存在。这种模式随脉冲标记时间有显著变化,并且需要添加RNA抑制剂来阻断追踪期间细胞内标记代谢物的再掺入。