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In Organello Transcription in Maize Mitochondria and Its Sensitivity to Inhibitors of RNA Synthesis

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Journal Plant Physiol
Specialty Physiology
Date 1987 Sep 1
PMID 16665676
Citations 6
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Abstract

Purified mitochondrial preparations from etiolated maize shoots support the incorporation of radioactivity from labeled UTP into RNA. The incorporation is linear with time for up to 2 hours, shows Michaelis-Menton kinetics with respect to the concentration of the labeled substrate, UTP, and has salt and pH optima which are different than those previously reported for RNA synthesis by isolated chloroplasts. When a crude mitochondrial preparation is subjected to isopycnic sucrose gradient centrifugation, the bulk of the RNA synthetic activity co-sediments with mitochondrial marker enzymes and with the mitochondrial 26S and 18S rRNAs. Maize mitochondrial RNA synthesis is prevented by actinomycin D and ethidium bromide but unaffected by alpha-amanitin. It is strongly inhibited by rifampicin at concentrations which have no effect on nuclear and chloroplast RNA synthesis, but only moderately inhibited by rifampicin at concentrations which completely inhibit bacterial RNA synthesis. The optimization, cell fractionation, and inhibitor data all suggest that contaminating organelles and bacteria do not contribute appreciably to the RNA synthesis in purified mitochondrial preparations.

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References
1.
Boutry M, Briquet M, Goffeau A . The alpha subunit of a plant mitochondrial F1-ATPase is translated in mitochondria. J Biol Chem. 1983; 258(14):8524-6. View

2.
Boerner P, Mason T, Fox T . Synthesis and processing of ribosomal RNA in isolated yeast mitochondria. Nucleic Acids Res. 1981; 9(23):6379-90. PMC: 327610. DOI: 10.1093/nar/9.23.6379. View

3.
Altman A, Cohen B, Weissbach H, Brot N . Transcriptional activity of isolated maize chloroplasts. Arch Biochem Biophys. 1984; 235(1):26-33. DOI: 10.1016/0003-9861(84)90251-0. View

4.
Brown G, Beattie D . Formation of the yeast mitochondrial membrane. V Differences in the assembly process of cytochrome oxidase and coenzyme QH2: cytochrome c reductase during respiratory adaptation. Biochim Biophys Acta. 1978; 538(2):173-87. DOI: 10.1016/0304-4165(78)90344-6. View

5.
Bottomley W, Spencer D, Wheeler A, Whitfeld P . The effect of a range of RNA polymerase inhibitors on RNA synthesis in higher plant chloroplasts and nuclei. Arch Biochem Biophys. 1971; 143(1):269-75. DOI: 10.1016/0003-9861(71)90209-8. View