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首页> 外文期刊>Acta Physiologiae Plantarum >High concentration of cadmium induces AtPCS2 gene expression in Arabidopsis thaliana (L.) Heynh ecotype Wassilewskija seedlings
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High concentration of cadmium induces AtPCS2 gene expression in Arabidopsis thaliana (L.) Heynh ecotype Wassilewskija seedlings

机译:高浓度的镉诱导拟南芥Heynh生态型Wassilewskija幼苗中AtPCS2基因表达

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In Arabidopsis thaliana, two genes encoding phytochelatin synthase (PCS; EC 2.3.2.15), AtPCS1 and AtPCS2, have been identified. Until now, only AtPCS1 was shown to play a role in response to Cd. To gain insight into the putative role of AtPCS2, three Cd concentrations (50, 100 and 200 μM) and long-term exposure (7 days) were tested on 1-week-old A. thaliana ecotype Wassilewskija (Ws) seedlings. Since 100 μM Cd did not alter seedling metabolism, as shown by unchanged total soluble protein and free proline contents, we investigated plantlet response to this concentration in addition to Cd accumulation. Seedlings accumulated Cd in roots and shoots. As phytochelatins and glutathione (GSH) contents increased in treated seedlings, we suggested that Cd might be translocated via the phytochelatin pathway. Specific enzymatic activities of γ-glutamylcysteine synthetase (GCS; EC 6.3.2.2), glutathione synthetase (GS; EC 6.3.2.3) and PCS were twice much more stimulated in shoots and roots after Cd exposure except GS that remained constant in shoots. As expression of genes encoding GCS and GS was unchanged in response to Cd, we suggested a regulation at translational or post-translational level. Surprisingly, AtPCS1 and AtPCS2 were differentially up-regulated after Cd treatment: AtPCS1 in shoots and AtPCS2 in whole plantlets. This last result suggests that PCS2 could be involved in plant response to high concentration of Cd in Ws ecotype and supports a putative role of PCS2, not redundant with PCS1, in a long-term response to Cd.
机译:在拟南芥中,已鉴定出编码植物螯合素合酶的两个基因(PCS; EC 2.3.2.15)AtPCS1和AtPCS2。到目前为止,只有AtPCS1被证明对Cd有反应。为了深入了解AtPCS2的假定作用,在1周龄拟南芥生态型Wassilewskija(Ws)幼苗上测试了三种Cd浓度(50、100和200μM)和长期暴露(7天)。由于100μMCd不会改变幼苗的代谢,如总可溶性蛋白和游离脯氨酸含量不变,我们除了Cd积累外,还研究了幼苗对这一浓度的响应。幼苗在根和芽中积累了镉。随着处理过的幼苗中植物螯合素和谷胱甘肽(GSH)含量的增加,我们建议镉可能通过植物螯合素途径转移。镉暴露后,芽和根中的γ-谷氨酰半胱氨酸合成酶(GCS; EC 6.3.2.2),谷胱甘肽合成酶(GS; EC 6.3.2.3)和PCS的特定酶活性被刺激了两倍多,但GS在芽中保持恒定。由于编码CCS和GS的基因对Cd的表达没有变化,因此我们建议在翻译或翻译后水平进行调控。令人惊讶的是,镉处理后AtPCS1和AtPCS2差异上调:芽中的AtPCS1和整个苗中的AtPCS2。最后的结果表明,PCS2可能参与植物对Ws生态型中高浓度Cd的响应,并在长期对Cd的响应中支持PCS2的假定作用,而不是PCS1多余。

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