Abstract
The specific rate of synthesis of tyrosine aminotransferase (EC 2.6.1.5; L-tyrosine:2-oxoglutarate aminotransferase) is used as a measure of the level of functional, cytoplasmic, tyrosine aminotransferase-specific mRNA in cultured rat hepatoma cells. An analysis of the kinetics of change in this rate after the addition or withdrawal of glucocorticosteroids sets an upper limit on the half-life of the enzyme-specific mRNA of 1-1.5 hr, whether or not steroid is present. The inactivation rate of the enzyme mRNA is independent of the growth condition of the cells, occuring equally rapidly in the presence or absence of serum or insulin, both of which induce tyrosine aminotransferase in these cells. The implications of these results for the mechanism of steroid induction are discussed.
MeSH Terms
Animals
Blood
Carcinoma, Hepatocellular/enzymology,metabolism
Cattle
Cells, Cultured
Computers
Dexamethasone/pharmacology
Enzyme Induction/drug effects
Insulin/pharmacology
Kinetics
Leucine/metabolism
Liver Neoplasms
Models, Chemical
Precipitin Tests
RNA, Messenger/metabolism
Rats
Tyrosine Transaminase/biosynthesis
Chemicals
Insulin
RNA, Messenger
Dexamethasone
Tyrosine Transaminase
Leucine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Steinberg R A
Levinson B B
Tomkins G M
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