[AtNHX1基因对黄芪的转化及其耐盐性表达]。

Yu Wei Zhao, Huai Yu Bu, Jian Gao Hao, Ying Juan Wang, Jing Fen Jia
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引用次数: 0

摘要

利用RT-PCR方法,从100 mmol/L NaCl预处理24h的拟南芥幼苗中克隆出编码空泡Na+/H+反转录子的AtNHX1-cDNA开放阅读框(ORF)。该ORF被插入到CaMV35S启动子、TMV RNA 5'UTR的Omega片段和二元表达载体pNT T-DNA区域的NOS polyA终止子之间(图1)。将重组质粒pNT-AtNHX1转化为农杆菌LBA4404。在该工程农杆菌介导下,将AtNHX1基因转移到第0代转基因麦香草株系中,获得了103株抗卡那霉素(Kanamycin)再生植株。通过对农杆菌浓度、感染时间、乙酰丁香酮(as)浓度等影响转化效率的因素进行优化,建立稳定的农杆菌介导的农家乐基因转化方案。部分T0转基因植株的PCR分析、Southern blot和RT-PCR检测表明,AtNHX1基因已明显整合到转基因植株的基因组中,并能正常转录。在相同的盐胁迫条件下,对野生型愈伤组织和转基因植株诱导的愈伤组织进行耐盐性检测,结果表明转基因愈伤组织的相对生长速度显著高于野生型愈伤组织。测定了转基因植株和野生型植株叶片中K+、Na+含量和相对电导率。由此可见,在不同浓度NaCl胁迫下,转基因植株细胞的K+/Na+比值始终高于野生型,而相对电导率则相反。综上所述,AtNHX1基因的转化不仅增强了转基因木香的耐盐性,而且减轻了盐对细胞膜的损伤。
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[Transformation of Astragalus melilotoides Pall with AtNHX1 gene and the expression of salinity tolerance of transformants].

Using RT-PCR method, the open reading frame (ORF) of AtNHX1-cDNA, encoding the vacuolar Na+/H+ antiportor, was cloned from Arabidopsis thaliana seedlings pretreated with 100 mmol/L NaCl for 24h. This ORF was inserted between CaMV35S promoter, a Omega fragment of TMV RNA 5'UTR and NOS polyA terminator in the T-DNA region of a binary expression vector pNT (Fig1). The recombinant plasmid, designated as pNT-AtNHX1, was then transformed into Agrobacterium tumefaciens LBA4404. Mediated by this engineering Agrobacterium, the AtNHX1 gene was transferred into T0 generation transgenic plant strains of A. melilotoides and 103 regenerated plants resistant to Kanamycin (Kan) were obtained. Some factors influencing the transformation efficiency, such as the concentration and infection duration of Agrobacterium, the concentration of Acetosyringone (AS), were optimized to establish a stable Agrobacterium mediated gene transformation protocol of A. melilotoides. PCR analysis, Southern blot and RT-PCR detection of some T0 transgenic plants showed that the AtNHX1 gene was evidently integrated into the genome of transgenic plants and couldl be transcripted properly. Under the same salt stress conditions, the detection of NaCl resistance revealed the difference between the wild-type calli and the transgenic calli that induced from the transgenic plants, i.e, the relative growth rates of the transgenic calli were remarkably higher than that of the wild-type calli. The K+ and Na+ contents and relative conductivity in the leaves of the transgenic plants and wild-type plants were estimated. It suggested that under the stress of different concentration of NaCl, K+/Na+ ratio in the transgenic plant cells were always higher than that in wild-type, however the situation of relative conductivity was on the opposite. From the facts above mentioned, the transformation of AtNHX1 gene not only enhanced the salt tolerance of transgenic A. melilotoides, but also reduced the cell membrane damage induced by salinity.

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