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线粒体丙酮酸脱氢酶。E1α亚基的分子克隆及表达分析。

Mitochondrial pyruvate dehydrogenase. Molecular cloning of the E1 alpha subunit and expression analysis.

作者信息

Grof C P, Winning B M, Scaysbrook T P, Hill S A, Leaver C J

机构信息

Department of Plant Sciences, University of Oxford, United Kingdom.

出版信息

Plant Physiol. 1995 Aug;108(4):1623-9. doi: 10.1104/pp.108.4.1623.

Abstract

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.

摘要

采用基于聚合酶链反应的方法,从高等植物中分离出编码线粒体丙酮酸脱氢酶E1α亚基的cDNA克隆。根据与非植物来源的E1α序列的相似性鉴定出推定的全长克隆。Southern印迹分析显示马铃薯(Solanum tuberosum L.)中有一小家族基因,而在黄瓜(Cucumis sativus)中只有一两个基因。在对不同马铃薯组织的Northern印迹分析中观察到E1α mRNA相对含量的组织特异性变化,在花组织中发现稳态转录水平最高。对黄瓜子叶中丙酮酸脱氢酶活性的测定表明,在吸胀后4至5天有一个短暂的增加至最大值。Western印迹分析显示E1α蛋白的量此时也达到峰值。发芽黄瓜子叶中的稳态转录水平也显示出短暂积累,在吸胀后2天达到峰值。这些数据与发芽后黄瓜子叶中E1α在转录和/或mRNA稳定性水平上的调控一致。

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