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激发子和胁迫处理后马铃薯中乙醇脱氢酶基因的表达

Alcohol dehydrogenase gene expression in potato following elicitor and stress treatment.

作者信息

Matton D P, Constabel P, Brisson N

机构信息

Department of Biochemistry, Université de Montréal, Canada.

出版信息

Plant Mol Biol. 1990 May;14(5):775-83. doi: 10.1007/BF00016510.

DOI:10.1007/BF00016510
PMID:2102855
Abstract

A cDNA clone corresponding to a mRNA that rapidly accumulates during the hypersensitive-like response induced by elicitor treatment of potato (Solanum tuberosum L.) tuber was characterized. The clone encodes a polypeptide (Mr = 41,097) having 83%-85% amino acid identity with known plant alcohol dehydrogenase sequences (ADH; EC 1.1.1.1). The identity of the clone was confirmed by measuring the ADH enzyme activity in extracts of Escherichia coli transformed with the cDNA clone. In potato tuber disks, a wide range of stresses, including treatment with fatty acid elicitors, salicylic acid, UV light and anaerobiosis, was shown to induce accumulation of Adh transcripts. In stems, a high constitutive level of Adh transcripts could be detected in 4-week old plants, but not in 8-week old plants. However, the mRNA could be induced to accumulate in stems of 8-week old plants by treatment with arachidonic acid elicitor or by anaerobiosis. Induction in leaves was also obtained during anaerobiosis and after treatment with a Phytophthora infestans mycelial homogenate.

摘要

对一个与信使核糖核酸(mRNA)对应的互补脱氧核糖核酸(cDNA)克隆进行了表征,该mRNA在激发子处理马铃薯(Solanum tuberosum L.)块茎诱导的类过敏反应期间迅速积累。该克隆编码一种多肽(分子量 = 41,097),与已知的植物乙醇脱氢酶序列(ADH;酶编号1.1.1.1)具有83%-85%的氨基酸同一性。通过测量用该cDNA克隆转化的大肠杆菌提取物中的ADH酶活性,证实了该克隆的同一性。在马铃薯块茎切片中,包括用脂肪酸激发子、水杨酸、紫外线和厌氧处理在内的多种胁迫被证明会诱导Adh转录本的积累。在茎中,在4周龄的植株中可检测到较高的Adh转录本组成水平,但在8周龄的植株中则检测不到。然而,通过用花生四烯酸激发子处理或厌氧处理,可诱导8周龄植株茎中的mRNA积累。在厌氧期间以及用致病疫霉菌丝体匀浆处理后,叶片中也出现了诱导现象。

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