John Short

Transcriptional and translational control of the biphasic increase in ornithine decarboxylase activity in liver.

Abstract The requirements for protein and RNA synthesis for each of the two increases in liver ornithine decarboxylase activity after the injection of unoperated rats with a solution containing glucagon and after 70% hepatectomy were studied with cycloheximide and actinomycin D. Protein synthesis is required for both increases whereas RNA formation is essential for the first elevation only. The second increase appears to be dependent upon RNA that is made during the period of the first rise in activity. The two rises in the decarboxylase activity may be caused by different stimuli. After the injection of the mixture with glucagon, the first elevation is accompanied by increases in hepatic tyrosine aminotransferase activity and in the rate of transport into liver cells of the model amino acid, α-aminoisobutyrate. Neither an increase in the aminotransferase activity nor in amino acid uptake occurs, however, during the period of the second elevation in the decarboxylase activity.

Loss of a Serum Protein from Hepatoma-Bearing Animals

A serum protein that is present in normal rat serum, and can be detected if serum is fractionated on polyacrylamide gel electrophoresis, disappears from the serum of hepatoma-bearing animals as the he