Oztetik E, Kockar F, Alper M, Iscan M
Department of Biology, Anadolu University, 26470 Eskisehir, Turkey.
J Genet. 2015 Sep;94(3):417-23. doi: 10.1007/s12041-015-0538-5.
Glutathione transferases (GSTs; EC 2.5.1.18) play important roles in stress tolerance and metabolic detoxification in plants.In higher plants, studies on GSTs have focussed largely on agricultural plants. There is restricted information about molecular characterization of GSTs in gymnosperms. To date, only tau class GST enzymes have been characterized from some pinus species. For the first time, the present study reports cloning and molecular characterization of two zeta class GST genes, namely PbGSTZ1 and PbGSTZ2 from Pinus brutia Ten., which is an economically important pine native to the eastern Mediterranean region and have to cope with several environmental stress conditions. The PbGSTZ1 gene was isolated from cDNA, whereas PbGSTZ2 was isolated from genomic DNA. Sequence analysis of PbGSTZ1 and PbGSTZ2 revealed the presence of an open reading frame of 226 amino acids with typical consensus sequences of the zeta class plant GSTs. Protein and secondary structure prediction analysis of two zeta class PbGSTZs have shared common features of other plant zeta class GSTs. Genomic clone, PbGSTZ2 gene, is unexpectedly intronless. Extensive sequence analysis of PbGSTZ2, with cDNA clone, PbGSTZ1, revealed 87% identity at nucleotide and 81% identity at amino acid levels with 41 amino acids differences suggesting that genomic PbGSTZ2 gene might be an allelic or a paralogue version of PbGSTZ1.
谷胱甘肽转移酶(GSTs;EC 2.5.1.18)在植物的胁迫耐受性和代谢解毒中发挥着重要作用。在高等植物中,对GSTs的研究主要集中在农作物上。关于裸子植物中GSTs分子特征的信息有限。迄今为止,仅从一些松树物种中鉴定出了tau类GST酶。本研究首次报道了从土耳其松(Pinus brutia Ten.)中克隆并鉴定了两个zeta类GST基因,即PbGSTZ1和PbGSTZ2,土耳其松是原产于地中海东部地区的一种具有重要经济价值的松树,必须应对多种环境胁迫条件。PbGSTZ1基因是从cDNA中分离出来的,而PbGSTZ2是从基因组DNA中分离出来的。对PbGSTZ1和PbGSTZ2的序列分析表明,存在一个由226个氨基酸组成的开放阅读框,具有zeta类植物GSTs的典型共有序列。对两个zeta类PbGSTZs的蛋白质和二级结构预测分析显示,它们具有其他植物zeta类GSTs的共同特征。基因组克隆PbGSTZ2基因意外地没有内含子。对PbGSTZ2与cDNA克隆PbGSTZ1进行的广泛序列分析表明,它们在核苷酸水平上的同一性为87%,在氨基酸水平上的同一性为81%,有41个氨基酸差异,这表明基因组PbGSTZ2基因可能是PbGSTZ1的等位基因或旁系同源物版本。