The activites of ornithine decarboxylase (ODC) and ODC inhibitory protein (ODC-antizyme) were studied in Ehrlich ascites tumor cells, separated according to their position in the cell cycle by centrifugal elutriation. Release and/or synthesis of ODC-antizyme was induced by putrescine treatment. Each
Cell-cycle-dependent expression of human ornithine decarboxylase
β Scribed by Leszek Kaczmarek; Bruno Calabretta; Sergio Ferrari; Jon K. de Riel
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 751 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
A human ornithine decarboxylase (ODC) gene probe has been isolated from a Jurkat T-cell cDNA expression library, sequenced, and used to analyze ODC mRNA levels in untransformed human lymphocytes and fibroblasts stimulated to proliferate by various mitogens. The partial cDNA sequence is 86% homologous to the mouse ODC cDNA, and Northern blots indicate that the human and mouse mRNA species are similar in size. ODC mRNA is barely detectable in quiescent human T lymphocytes and undetectable in densityarrested W138 fibroblasts. Following stimulation of T-lymphocyte proliferation with phytohemagglutinin, the ODC mRNA level rises to a peak around mid GI phase and decreases as t h e cells enter S phase. Serum stimulation of density-arrested fibroblasts results in an elevation of the ODC mRNA level which persists throughout the cell cycle. Epidermal growth factor (20 ng/ml) but not insulin (10 mglml) or dexamethasone (55 nglml) stimulates ODC expression in quiescent W138 fibroblasts. Southern blots suggest that human celIs have a single copy of the ODC gene.
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