Mitochondrial pyruvate dehydrogenase: molecular cloning of the E1 alpha subunit and expression analysis

A polymerase chain reaction-based approach was used to isolate cDNA clones encoding the E1 alpha subunit of the mitochondrial pyruvate dehydrogenase from higher plants. Putative full-length clones were identified on the basis of similarity to E1 alpha sequences from nonplant sources. Southern blot a...

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Veröffentlicht in:Plant physiology (Bethesda) 1995-08, Vol.108 (4), p.1623-1629
Hauptverfasser: Grof, C.P.L. (Commonwealth Scientific and Industrial Research Organization, Queensland, Australia.), Winning, B.M, Scaysbrook, T.P, Hill, S.A, Leaver, C.J
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Sprache:eng
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Zusammenfassung:A polymerase chain reaction-based approach was used to isolate cDNA clones encoding the E1 alpha subunit of the mitochondrial pyruvate dehydrogenase from higher plants. Putative full-length clones were identified on the basis of similarity to E1 alpha sequences from nonplant sources. Southern blot analysis revealed a small family of genes in potato (Solanum tuberosum L.), whereas in cucumber (Cucumis sativus) there are only one or two genes. Tissue-specific variation in the relative amounts of E1 alpha mRNA was observed in northern blot analysis of different potato tissues, with the highest steady-state transcript levels found in floral tissue. Measurement of pyruvate dehydrogenase activity in cucumber cotyledons showed that there is a transient increase to a maximum at 4 to 5 d postimbibition. Western blot analysis revealed that the amount of E1 alpha protein also peaks at this time. Steady-state transcript levels in germinating cucumber cotyledons also show transient accumulation, peaking 2 d postimbibition. These data are consistent with regulation of E1 alpha at the level of transcription and/or mRNA stability in postgerminative cucumber cotyledons
ISSN:0032-0889
1532-2548
DOI:10.1104/pp.108.4.1623