Department of Plant Sciences, University of Saskatchewan, Saskatoon, SK, S7N 0P5, Canada.
Mol Biol Rep. 2013 Dec;40(12):6593-603. doi: 10.1007/s11033-013-2772-3. Epub 2013 Sep 22.
Antioxidant system is one of the important factors in regulating plant growth, development and adaptation. Thus, in order to have better insights into molecular mechanisms of growth and adaptation of a plant it is prerequisite to have known the status of various components of the antioxidant system of the plant. Here we studied the status of enzymatic and non-enzymatic components of the antioxidant system of picrorhiza (Picrorhiza kurrooa). Picrorhiza is an important medicinal herb of western Himalayan region and has been listed in the Red Data Book as an endangered species. Spatio-temporal analysis of ascorbic acid and glutathione in leaf, root and rhizome during different stages of development revealed differential status of these antioxidant molecules. Of the three tissues, ascorbic acid was found to be highest in leaves and lowest in roots. Interestingly, just opposite to that, glutathione was highest in roots and lowest in leaves. Using degenerate primers based approach followed by rapid amplification of complementary DNA (cDNA) ends method, full length cDNAs of three important genes namely Picrorhiza kurrooa ascorbate peroxidase (pkapx), Picrorhiza kurrooa monodehydroascorbate reductase (pkmdhar) and Picrorhiza kurrooa glutathione reductase (pkgr) of antioxidant system were cloned from picrorhiza. Complementary DNAs of pkapx, pkmdhar and pkgr contained 1,049, 2,016 and 1,664 bp, respectively. Expression analysis showed differential spatio-temporal expression of these genes. Expressions of all the three genes were found higher in roots as compared to rhizome and leaves. Temporal expression analysis of pkapx, pkmdhar and pkgr revealed differential transcript levels. Expression of pkapx exhibited negative correlation with the light intensity. Just opposite to the pkapx, expression pattern of pkgr revealed its positive correlation with light intensity. Expression pattern of pkmdhar revealed its light independent expression behavior. The findings may be useful to assess the role of cloned genes in picrorhiza growth, adaptation and can further be utilized for transgenic development for desired trait(s).
抗氧化系统是调节植物生长、发育和适应的重要因素之一。因此,为了更好地了解植物生长和适应的分子机制,必须了解植物抗氧化系统各种成分的状况。在这里,我们研究了獐牙菜(Picrorhiza kurrooa)抗氧化系统的酶和非酶成分的状况。獐牙菜是喜玛拉雅西部地区的一种重要药用植物,已被列入濒危物种红色名录。在不同发育阶段的叶片、根和根茎中,对抗坏血酸和谷胱甘肽的时空分析揭示了这些抗氧化分子的不同状态。在这三种组织中,发现叶片中的抗坏血酸含量最高,而根部中的含量最低。有趣的是,正好相反,谷胱甘肽在根部中的含量最高,而在叶片中的含量最低。使用基于简并引物的方法,然后使用快速扩增 cDNA 末端(RACE)方法,从獐牙菜中克隆了抗氧化系统的三个重要基因,即 Picrorhiza kurrooa 抗坏血酸过氧化物酶(pkapx)、Picrorhiza kurrooa 单脱氢抗坏血酸还原酶(pkmdhar)和 Picrorhiza kurrooa 谷胱甘肽还原酶(pkgr)的全长 cDNA。pkapx、pkmdhar 和 pkgr 的 cDNA 分别包含 1049、2016 和 1664bp。表达分析显示这些基因的时空表达存在差异。与根茎和叶片相比,所有三个基因在根部的表达都较高。pkapx、pkmdhar 和 pkgr 的时间表达分析显示了不同的转录水平。pkapx 的表达与光强度呈负相关。与 pkapx 相反,pkgr 的表达模式显示其与光强度呈正相关。pkmdhar 的表达模式显示其具有独立于光的表达行为。这些发现可能有助于评估克隆基因在獐牙菜生长、适应中的作用,并可进一步用于转基因开发以获得所需的特性。