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A nuclear gene encoding mitochondrial proline dehydrogenase an enzyme involved in proline metabolism is upregulated by proline but downregulated by dehydration in Arabidopsis.

机译:在拟南芥中编码线粒体脯氨酸脱氢酶(一种参与脯氨酸代谢的酶)的核基因被脯氨酸上调但由于脱水而下调。

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摘要

Proline is one of the most common compatible osmolytes in water-stressed plants. The accumulation of proline in dehydrated plants is caused both by the activation of proline biosynthesis and by the inactivation of proline degradation; a decrease in the level of accumulated proline in rehydrated plants is caused both by the inhibition of proline biosynthesis and by the activation of proline degradation. The proline biosynthetic pathway has been well characterized, but the degradation of proline is poorly understood. Sequence analysis of an Arabidopsis cDNA clone, ERD5 (for early responsive to dehydration stress), isolated from plants dehydrated for 1 hr, revealed that it encodes a protein with identity to products of the yeast PUT1 (for proline utilization) gene (23.6% over 364 amino acids) and the Drosophila sluggish-A gene (34.5% over 255 amino acids). Their gene products are precursors of proline oxidases (dehydrogenase) (EC 1.5.99.8), which are the first enzymes involved in the conversion of proline to glutamic acid. Proline oxidase is localized in mitochondria. RNA gel blot analysis demonstrated that transcripts of the ERD5 gene were undetectable when plants had been dehydrated for 10 hr, but large amounts of the transcript accumulated when plants subsequently were rehydrated. Elevated levels of the transcript were also found in plants that had been incubated in a medium that contained proline. Immunologically, we showed that the product of ERD5 is localized in the mitochondrial fraction and accumulates in response to proline in cultured cells. Fusion genes for ERD5 and PUT1 complemented a put1 mutant of yeast, allowing put1 to grow with proline as the source of nitrogen. These results suggest that ERD5 encodes a precursor of proline dehydrogenase (oxidase), which is regulated at the level of mRNA accumulation in both dehydrated and rehydrated plants.
机译:脯氨酸是水分胁迫植物中最常见的相容渗透压剂之一。脯氨酸在脱水植物中的积累是由脯氨酸生物合成的激活和脯氨酸降解的失活引起的。脯氨酸生物合成的抑制和脯氨酸降解的激活都导致了水合植物中脯氨酸积累水平的下降。脯氨酸的生物合成途径已被很好地表征,但是对脯氨酸的降解了解得很少。从脱水1小时的植物中分离出来的拟南芥cDNA克隆ERD5(对脱水胁迫的早期响应)的序列分析表明,它编码的蛋白质与酵母PUT1(脯氨酸利用)基因的产物具有相同性(超过23.6%)果蝇(Drosophila)迟缓-A基因(364个氨基酸)(255个氨基酸上占34.5%)。它们的基因产物是脯氨酸氧化酶(脱氢酶)(EC 1.5.99.8)的前体,是涉及脯氨酸向谷氨酸转化的首批酶。脯氨酸氧化酶位于线粒体中。 RNA凝胶印迹分析表明,当植物脱水10小时后,ERD5基因的转录物是不可检测的,但是当植物随后再水化时,大量的转录物会积累。在含有脯氨酸的培养基中孵育的植物中也发现转录物水平升高。免疫学上,我们显示ERD5的产物位于线粒体部分,并在培养细胞中响应脯氨酸而积累。 ERD5和PUT1的融合基因补充了酵母的put1突变体,使put1以脯氨酸为氮源生长。这些结果表明,ERD5编码脯氨酸脱氢酶(氧化酶)的前体,脯氨酸脱氢酶(氧化酶)在脱水和再水化植物中均受mRNA积累水平的调节。

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