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Relationship of Cellular Energetics to RNA Metabolism in Tetrahymena pyriformis W. *
Author(s) -
CONNER ROBERT L.,
KOROLY MARY J.
Publication year - 1974
Publication title -
the journal of protozoology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 0022-3921
DOI - 10.1111/j.1550-7408.1974.tb03634.x
Subject(s) - biochemistry , oxidative phosphorylation , uracil , rna , nucleic acid , glycolysis , tetrahymena pyriformis , tetrahymena , dinitrophenol , biology , citric acid cycle , metabolism , chemistry , dna , gene
SYNOPSIS Cultures of Tetrahymena pyriformis in a non‐nutrient buffer degrade RNA and excrete hypoxanthine, uracil and orthophosphate. Glucose addition leads to the retention of a portion of the purine, pyrimidine, and orthophosphate by the cells; however, the hexose has little influence on the RNA level. Acetate supplementation has no effect on RNA degradation or on the distribution of the catabolic products between the cells and the environment. Interruption of oxidative phosphorylation by 2,4‐dinitrophenol results in an increase in RNA degradation. This action is annulled by the glycolytic substrate, glucose, but not by acetate. A combination of iodoacetic acid and glucose blocks glycolysis and increases cellular RNA loss which can be reversed by the addition of the citric acid cycle substrate, acetate. These findings suggest that the available cellular energy supply in starved cells is sufficient to regulate the rate of RNA degradation. Disruption of ATP generation by the appropriate inhibitors, however, allows the demonstration of the importance of energy‐yielding reactions in the determination of the amount of nucleic acid loss. It appears that glycolysis and oxidative phosphorylation are equally efficient in sustaining the regulatory process. RNA synthesis during starvation conditions is a discontinuous process with a sharp rate change after 30 min of incubation. 2,4‐Dinitrophenol inhibits [2‐ 14 C] uracil incorporation into the nucleic acid. Glucose does not annul the inhibition of synthesis in contrast to the influence of the hexose on RNA degradation. This observation demonstrates that the synthetic and degradative processes are not directly coupled. Glycogen synthesis and RNA degradation appear to compete for the available energy supply and respond in a similar fashion to the metabolic inhibitors and carbon sources.