Molecular cloning and characterization of a glutathione S-transferase gene from Ginkgo biloba.

Xuefen Liu, Zhongxiang Deng, Shi Gao, Xiaofen Sun, Kexuan Tang
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引用次数: 7

Abstract

Glutathione S-transferases (GSTs) play an important role in the response of plants to changing environmental conditions. Here, we report the cloning of the GST gene for GST from Ginkgo biloba, a native medicinal plant species in China, by rapid amplification of cDNA ends (RACE). The full-length cDNA (designated as GbGST) was 1008 bp and contained a 684 bp open reading frame (ORF) encoding a polypeptide of 228 amino acids. The genomic sequence of GbGST was also obtained. Semi-quantitative RT-PCR analysis revealed that GbGST expressed in all tested tissues of G. biloba, including leaf, root and stem and the expression of GbGST could be induced by UV, MJ and drought treatments, suggesting that GbGST was potentially involved in plant's stress tolerance. To our knowledge, this is the first GST cDNA cloned from Ginkgoaceae. Based on comparative analyses of amino acid sequence, phylogeny, predicted three-dimensional structure together with the gene structure, the GbGST should be classified into the tau class.

银杏谷胱甘肽s -转移酶基因的克隆与鉴定。
谷胱甘肽s -转移酶(GSTs)在植物对环境变化的响应中起着重要作用。本文报道了利用cDNA末端快速扩增技术(RACE)从中国本土药用植物银杏中克隆GST基因。该cDNA全长1008 bp,包含一个684 bp的开放阅读框(ORF),编码228个氨基酸的多肽。获得了GbGST的基因组序列。半定量RT-PCR分析显示,GbGST在枇杷叶、根、茎等组织中均有表达,且在UV、MJ和干旱处理下均可诱导表达,表明GbGST可能参与植物的抗逆性。据我们所知,这是第一个从银杏科植物中克隆到的GST cDNA。基于氨基酸序列、系统发育、预测三维结构及基因结构的比较分析,GbGST应归为tau类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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