The events occurring during emergence of cells from quiescence ("Go") are not necessarily identical to those in the G, phase of continuously dividing cells. Cellular levels of t h e mRNAs coding for ornithine decarboxylase (ODC) and S-adenosyl-methionine decarboxylase (SDC), key enzymes in polyamine
Polyamine biosynthesis and accumulation during the G1 to S phase transition
β Scribed by David J. M. Fuller; Eugene W. Gerner; Diane Haddock Russell
- Book ID
- 102880954
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 703 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Abstract
Ornithine decarboxylase, an important enzyme in growth regulation, is increased in CHO cells in G~1~ phase of the cell cycle and decreases as the cells progress into S phase. SβadenosylβLβmethionine decarboxylase activity, which is dependent on either the presence of putrescine or spermidine for the synthesis of spermidine and spermine respectively, shows a maximal increase in late G~1~/early S phase which corresponds very closely with the cell cycle phase specific accumulation of spermidine and spermine during S phase. Total culture evaluation of spermidine and spermine, which included extracellular as well as intracellular concentrations, indicated that extracellular accumulations of these polyamines occurred only in G~1~ and that entry into S phase was concomitant with intracellular accumulation patterns. Hyperthermia (43Β°C for 1 hour) in midβG~1~ phase of the cell cycle resulted in rapid decreases in the activities of ornithine decarboxylase and SβadenosylβLβmethionine decarboxylase. In these cells, DNA replication was also not detectable until nine hours after mitosis, a time at which there had been recovery of ornithine decarboxylase and SβadenosylβLβmethionine decarboxylase activities. Previous data have further indicated a requirement for polyamine reaccumulation before control DNA replication rates are resumed. We therefore suggest that polyamine biosynthesis and intracellular accumulation are both temporal and quantitative prerequisites for transition through S phase.
π SIMILAR VOLUMES
## Abstract Biochemical events were investigated in the G1 to S phase progression induced in quiescent rodent cells by human adenovirus type 5 (Ad5) and by serum. Thymidine kinase activity increased after infection of cells with Ad5 or addition of 10% serum. These stimulations were additive. An ear