Becher Martina, Talke Ina N, Krall Leonard, Krämer Ute
Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, D-14476 Golm, Germany.
Plant J. 2004 Jan;37(2):251-68. doi: 10.1046/j.1365-313x.2003.01959.x.
Arabidopsis halleri ssp. halleri (accession Langelsheim) is a naturally selected zinc (Zn)- and cadmium-tolerant Zn hyperaccumulator. This plant differs strikingly from its close relative A. thaliana by accumulating Zn specifically in above-ground tissues. A. thaliana GeneChips were used in order to identify, on a transcriptome-wide scale, genes with a potential involvement in cellular metal uptake or detoxification in the shoots of A. halleri. Compared to A. thaliana, transcript abundance of several genes was found and confirmed to be substantially higher in A. halleri after 4 days of exposure to low as well as high Zn concentrations in the hydroponic culture medium. The identified candidate genes encode proteins closely related to the following A. thaliana proteins: AtZIP6, a putative cellular Zn uptake system and member of the zinc-regulated transporter (ZRT)-iron regulated transporter (IRT)-like protein (ZIP)-family of metal transporters, the putative P-type metal ATPase AtHMA3, the cation diffusion facilitator ZAT/AtCDF1, and the nicotianamine synthase AtNAS3. Heterologous expression in mutant strains of the yeast Saccharomyces cerevisiae suggested that AhHMA3, AhCDF1-3, and AhNAS3 can function in cellular Zn detoxification. Our data indicate that, at the transcript level, the Zn tolerance strategy of A. halleri involves high constitutive expression of metal homeostasis genes in the shoots to accommodate higher basal levels of Zn accumulation, and possibly to prepare for sudden increases in Zn influx into shoot cells. Furthermore, profiling of metal homeostasis gene transcripts in shoot and root tissues by real-time RT-PCR indicated that A. halleri and A. thaliana respond differently to changes in plant Zn status.
拟南芥(Arabidopsis halleri ssp. halleri,登录号Langelsheim)是一种经自然选择的耐锌(Zn)和镉的锌超积累植物。这种植物与它的近缘种拟南芥(A. thaliana)有显著差异,它能将锌特异性地积累在地上组织中。为了在转录组范围内鉴定拟南芥地上部分中可能参与细胞金属吸收或解毒的基因,使用了拟南芥基因芯片。与拟南芥相比,在水培培养基中分别暴露于低锌和高锌浓度4天后,发现并证实拟南芥中几个基因的转录丰度显著高于拟南芥。鉴定出的候选基因编码的蛋白质与以下拟南芥蛋白质密切相关:AtZIP6,一种假定的细胞锌吸收系统,属于金属转运蛋白的锌调节转运体(ZRT)-铁调节转运体(IRT)-样蛋白(ZIP)家族;假定的P型金属ATP酶AtHMA3;阳离子扩散促进因子ZAT/AtCDF1;以及烟酰胺合酶AtNAS3。在酿酒酵母(Saccharomyces cerevisiae)突变菌株中的异源表达表明,AhHMA3、AhCDF1 - 3和AhNAS3可在细胞锌解毒中发挥作用。我们的数据表明,在转录水平上,拟南芥的耐锌策略涉及地上部分金属稳态基因的高组成型表达,以适应更高的基础锌积累水平,并可能为锌流入地上细胞的突然增加做好准备。此外,通过实时RT-PCR对地上和根组织中金属稳态基因转录本进行分析表明,拟南芥和拟南芥对植物锌状态变化的反应不同。