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Mol Cell Biochem ; 221(1-2): 3-10, 2001 May.
Article in English | MEDLINE | ID: mdl-11506183

ABSTRACT

Rat liver mitochondria respond to changes in energy demand by modulating the amount of RNA synthesized. Coupled rat liver mitochondria were used to determine the relationship between mitochondrial respiration, ATP levels, and mitochondrial transcription. This system included oxidizable substrates (malate and glutamate) and constituents that could support both mitochondrial respiration and transcription. The respiratory inhibitor rotenone, phosphorylation inhibitor oligomycin, and the uncoupler of oxidative phosphorylation carbonyl-cyanide p-triflouromethoxyphehylhydrazone inhibited RNA synthesis. Addition of ADP stimulated mitochondrial transcription and peak RNA synthesis was observed at 1-2 mM ADP. At ADP concentrations above 2 mM, RNA synthesis decreased. These results demonstrate that mitochondrial transcription is tightly coupled to ATP levels.


Subject(s)
Adenosine Triphosphate/biosynthesis , Mitochondria, Liver/metabolism , RNA/biosynthesis , Transcriptional Activation , Adenosine Diphosphate/pharmacology , Animals , Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone/pharmacology , Cell Respiration , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Enzyme Inhibitors/pharmacology , Oligomycins/pharmacology , Oxygen Consumption , Phosphorylation/drug effects , RNA, Messenger/biosynthesis , RNA, Mitochondrial , Rats , Rotenone/pharmacology , Time Factors , Transcription, Genetic/drug effects , Uncoupling Agents/pharmacology
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