Key Laboratory of Forest Tree Genetics Improvement and Biotechnology, Ministry of Education, Northeast Forestry University, 26 Hexing Road, Harbin 150040, China.
Mol Biol Rep. 2011 Oct;38(7):4813-22. doi: 10.1007/s11033-010-0624-y. Epub 2010 Dec 14.
We have cloned a Na(+)/H(+) antiporter gene (GenBank accession no EF440291, PtNHA1) from Puccinellia tenuiflora (so-called alkali grass in Chinese) roots under NaCl salt stress. Its cDNA is 3775 bp and contains a 3414 bp open reading frame. The amino acid sequences of PtNHA1 show high identities with a putative plasma membrane Na(+)/H(+) antiporter from wheat. PtNHA1 was predicted to contain 11 hypothetical transmembrane domains in the N-terminal part and to localize in the plasma membrane. Genomic DNA gel blot analysis shows that PtNHA1 is a single-copy gene in the alkali grass genome. PtNHA1 is highly expressed in leaves, roots and shoots by RNA gel blot analysis. Furthermore, PtNHA1 gene expression of alkali grass was clearly up-regulated by NaCl salt stress. Overexpression of PtNHA1 in Arabidopsis resulted in enhanced tolerance of transgenic plants to NaCl stress. The ion contents analysis shows that, compared with the wild-type (WT), less Na(+) and more K(+) were accumulated in transgenic plants under NaCl stress. The results indicate that PtNHA1 play an important role in NaCl salt stress. Additionally, compared with the WT, total activities of ascorbate peroxidase (APX) and catalase (CAT), two key reactive oxygen species (ROS) detoxifying enzymes were high in transgenic plants under salt stress, respectively. The transcript levels of two APX genes (Apx1, s/mApx) and two CAT genes (Cat1, Cat2) in transgenic plants were higher than those in WT. This suggests that overexpression of PtNHA1 results in enhanced ROS-scavenging enzymes of transgenic plants under NaCl salt stress.
我们从盐胁迫下的星星草(中国俗称碱草)根中克隆了一个 Na(+)/H(+) 反向转运蛋白基因(GenBank 登录号 EF440291,PtNHA1)。其 cDNA 长 3775bp,包含一个 3414bp 的开放阅读框。PtNHA1 的氨基酸序列与小麦中一种假定的质膜 Na(+)/H(+) 反向转运蛋白具有高度同源性。PtNHA1 被预测含有 11 个假定的跨膜结构域,位于 N 端,定位于质膜上。基因组 DNA 凝胶印迹分析表明,PtNHA1 是碱草基因组中的单拷贝基因。PtNHA1 在叶片、根和茎中的 RNA 凝胶印迹分析中表达量较高。此外,PtNHA1 基因在碱草中对 NaCl 盐胁迫的表达明显上调。PtNHA1 在拟南芥中的过表达导致转基因植物对 NaCl 胁迫的耐受性增强。离子含量分析表明,与野生型(WT)相比,在 NaCl 胁迫下,转基因植物积累的 Na(+) 较少,K(+) 较多。结果表明 PtNHA1 在 NaCl 盐胁迫中发挥重要作用。此外,与 WT 相比,在盐胁迫下,转基因植物中两种关键活性氧(ROS)解毒酶抗坏血酸过氧化物酶(APX)和过氧化氢酶(CAT)的总活性分别升高。转基因植物中两个 APX 基因(Apx1、s/mApx)和两个 CAT 基因(Cat1、Cat2)的转录水平均高于 WT。这表明,PtNHA1 的过表达导致转基因植物在 NaCl 盐胁迫下增强了 ROS 清除酶。