CAJ | 학술논문

植物响应盐胁迫逆境，涉及一系列的保护酶类基因的表达和调控， SOD酶是其中重要的一类。本研究通过对盐胁迫后7个柽柳转录组分析和进一步测序验证，获得了2个柽柳FeSOD基因全长cDNA序列，它们编码蛋白的氨基酸残基数分别为256、308，分子量为63.8、75.4 kDa，理论等电点为5.0和5.1。实时荧光定量PCR结果显示这2个FeSOD基因在盐胁迫后柽柳根和叶中呈现不同的表达模式。在根中，第9天时， ThFeSOD1和ThFeSOD2基因的表达均明显上调。在叶中， ThFeSOD1和ThFeSOD2在胁迫3天受明显的诱导，而5天表达受明显的抑制。
식물향응염협박역경，섭급일계렬적보호매류기인적표체화조공， SOD매시기중중요적일류。본연구통과대염협박후7개정류전록조분석화진일보측서험증，획득료2개정류FeSOD기인전장cDNA서렬，타문편마단백적안기산잔기수분별위256、308，분자량위63.8、75.4 kDa，이론등전점위5.0화5.1。실시형광정량PCR결과현시저2개FeSOD기인재염협박후정류근화협중정현불동적표체모식。재근중，제9천시， ThFeSOD1화ThFeSOD2기인적표체균명현상조。재협중， ThFeSOD1화ThFeSOD2재협박3천수명현적유도，이5천표체수명현적억제。
For plants, some protecting enzymes were involved in the response to abiotic stress as salt , drought, low temperature and heat stress , and the superoxide dismutase ( SOD) proteins is one of the important antioxidase types.2 full length cDNA of ThFeSOD genes were cloned from 7 transcriptome cDNA library of Tamarix hispida.in this study , and these 2 ThFeSOD genes encoded proteins of 256 and 308 amino acid residues with the molecular mass of 63.8-kDa and 75.4-kDa and theoretical isoelectric point of 5.0 and 5.1, respectively.The results of real time RT-PCR showed that the expressions of these 2 ThFeSOD genes were different in roots and leaves under NaCl stress.In roots, their expression were obvious induced at 9 d.In leaves, the expression levels of 2 ThFeSOD genes were upregulated at 3 d, while downregulated at 5 d.