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复苏植物粘叶旱生草中的保护机制:编码肌醇-1-磷酸合酶的基因XvINO1的克隆、表达、特性及作用

Protection mechanisms in the resurrection plant Xerophyta viscosa: cloning, expression, characterisation and role of XvINO1, a gene coding for a myo-inositol 1-phosphate synthase.

作者信息

Lehner Arnaud, Chopera Denis R, Peters Shaun W, Keller Felix, Mundree Sagadevan G, Thomson Jennifer A, Farrant Jill M

机构信息

University of Cape Town, Department of Molecular and Cellular Biology, Private Bag, Rondebosch 7701, Cape Town, South Africa.

University of Zürich, Institute of Plant Biology, Molecular Plant Physiology, Zollikerstrasse 107, Zürich, 8008, Switzerland.

出版信息

Funct Plant Biol. 2008 Feb;35(1):26-39. doi: 10.1071/FP07142.

Abstract

We have used reverse transcription-PCR coupled with 5'- and 3'-RACE to isolate a full length INO1 cDNA (1692 bp with an ORF of 1530) from the resurrection plant Xerophyta viscosa Baker. XvINO1 encodes 510 amino acids, with a predicted MW of 56.7kD and contains four sequence motifs that are highly conserved in plant myo-inositol-1-phosphate synthases (MIPS, EC5.5.1.4), the enzyme that catalyses the first step in the formation of myo-inositol (Ino). Northern and western analyses show that the transcript and protein are constitutively present in leaves but their expression increases, temporarily, in response to both accumulative salt stress (~300 mM NaCl) and desiccation (to 5% relative water content). Leaf Ino concentration increases 40-fold during the first 6 h of salt stress, and levels of this and other carbohydrates (galactinol, sucrose, raffinose, stachyose and hexoses) remain elevated relative to control leaves for the duration of salt stress treatment. The timing and pattern of accumulation of these carbohydrates differ under desiccation stress and we propose that they perform different functions in the respective stresses. These are elaborated in discussion of our data.

摘要

我们利用逆转录聚合酶链反应(RT-PCR)结合5'-和3'-RACE技术,从复苏植物粘叶旱生草(Xerophyta viscosa Baker)中分离出一个全长INO1 cDNA(1692 bp,开放阅读框为1530)。XvINO1编码510个氨基酸,预测分子量为56.7kD,包含四个在植物肌醇-1-磷酸合酶(MIPS,EC5.5.1.4)中高度保守的序列基序,该酶催化肌醇(Ino)形成的第一步。Northern和western分析表明,转录本和蛋白质在叶片中组成性存在,但它们的表达会因累积盐胁迫(约300 mM NaCl)和干燥(至相对含水量5%)而暂时增加。在盐胁迫的前6小时内,叶片Ino浓度增加40倍,并且在盐胁迫处理期间,其以及其他碳水化合物(半乳糖醇、蔗糖、棉子糖、水苏糖和己糖)的水平相对于对照叶片保持升高。这些碳水化合物在干燥胁迫下积累的时间和模式不同,我们认为它们在各自的胁迫中发挥不同的功能。我们将在数据讨论中详细阐述这些内容。

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