Filippova G N, Borovkova O V, Alesenko A V
Biokhimiia. 1991 May;56(5):892-902.
Using a model of cycloheximide (CHI)-induced expression of nuclear oncogens, a comparative study of metabolism of the major lipid classes in rat liver nuclei and cells was carried out. A short-term activation of sphingomyelinase which preceded on a time scale the maximal accumulation of c-fos and c-myc transcripts was observed both in the cells and in the nuclei. In contrast with the whole cell, the level of phospholipase C activity in the nuclei did not change under conditions of oncogene activation. It was found that the maximal expression of nuclear oncogens coincided in time with cyclic changes in the content of practically all phospholipids and neutral lipids with simultaneous activation of their synthesis both in the cells and in the nuclei. However, in the nuclei the sphingomyelin metabolism activation was predominant. It is concluded that in the nucleus sphingomyelin and its metabolites may influence oncogene expression via nuclear protein kinase C.
利用环己酰亚胺(CHI)诱导核致癌基因表达的模型,对大鼠肝细胞核与细胞中主要脂质类别的代谢进行了比较研究。在细胞和细胞核中均观察到,鞘磷脂酶的短期激活在时间上先于c-fos和c-myc转录本的最大积累。与整个细胞不同,在致癌基因激活的条件下,细胞核中磷脂酶C的活性水平没有变化。研究发现,核致癌基因的最大表达与几乎所有磷脂和中性脂质含量的周期性变化在时间上相吻合,同时细胞和细胞核中它们的合成均被激活。然而,在细胞核中鞘磷脂代谢的激活占主导地位。得出的结论是,在细胞核中鞘磷脂及其代谢产物可能通过核蛋白激酶C影响致癌基因的表达。