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δ-1-吡咯啉-5-羧酸合成酶和脯氨酸脱氢酶基因的相互调控在植物渗透胁迫期间及之后控制脯氨酸水平。

Reciprocal regulation of delta 1-pyrroline-5-carboxylate synthetase and proline dehydrogenase genes controls proline levels during and after osmotic stress in plants.

作者信息

Peng Z, Lu Q, Verma D P

机构信息

Department of Plant Biology, Ohio State University, Columbus 43210, USA.

出版信息

Mol Gen Genet. 1996 Dec 13;253(3):334-41. doi: 10.1007/pl00008600.

Abstract

Plants generally accumulate free proline under osmotic stress conditions. Upon removal of the osmotic stress, the proline levels return to normal. In order to understand the mechanisms involved in regulating the levels of proline, we cloned and characterized a proline dehydrogenase (PDH) cDNA from Arabidopsis thaliana (AtPDH). The 1745 bp cDNA contains a major open reading frame encoding a peptide of 499 amino acids. The deduced amino acid sequence has high homology with both Saccharomyces cerevisiae and Drosophila melanogaster proline oxidases and contains a putative mitochondrial targeting sequence. When expressed in yeast, the AtPDH cDNA complemented a yeast put1 mutation and exhibited proline oxidase activity. We also determined the free proline contents and the delta 1-pyrroline-5-carboxylate synthetase (P5CS) and PDH mRNA levels under different osmotic stress and recovery conditions. The results demonstrated that the removal of free proline during the recovery from salinity or dehydration stress involves an induction of the PDH gene while the activity of P5CS declines. The reciprocal regulation of P5CS and PDH genes appears to be a key mechanism in the control of the levels of proline during and after osmotic stress. The PDH gene was also significantly induced by exogenously applied proline. The induction of PDH by proline, however, was inhibited by salt stress.

摘要

植物通常在渗透胁迫条件下积累游离脯氨酸。去除渗透胁迫后,脯氨酸水平恢复正常。为了了解调节脯氨酸水平的机制,我们从拟南芥中克隆并鉴定了一个脯氨酸脱氢酶(PDH)cDNA(AtPDH)。这个1745 bp的cDNA包含一个主要的开放阅读框,编码一个499个氨基酸的肽段。推导的氨基酸序列与酿酒酵母和黑腹果蝇的脯氨酸氧化酶都有高度同源性,并包含一个假定的线粒体靶向序列。当在酵母中表达时,AtPDH cDNA弥补了酵母put1突变并表现出脯氨酸氧化酶活性。我们还测定了不同渗透胁迫和恢复条件下的游离脯氨酸含量以及δ1-吡咯啉-5-羧酸合成酶(P5CS)和PDH mRNA水平。结果表明,在从盐胁迫或脱水胁迫恢复过程中游离脯氨酸的去除涉及PDH基因的诱导,而P5CS的活性下降。P5CS和PDH基因的相互调节似乎是渗透胁迫期间和之后脯氨酸水平控制的关键机制。外源施加脯氨酸也能显著诱导PDH基因。然而,脯氨酸对PDH的诱导受到盐胁迫的抑制。

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