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首页> 外文期刊>Plant and Cell Physiology >A Mutant Strain Arabidopsis thaliana that Lacks Vacuolar Membrane Zinc Transporter MTP1 Revealed the Latent Tolerance to Excessive Zinc
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A Mutant Strain Arabidopsis thaliana that Lacks Vacuolar Membrane Zinc Transporter MTP1 Revealed the Latent Tolerance to Excessive Zinc

机译:缺少液泡膜锌转运蛋白MTP1的突变株拟南芥揭示了对过量锌的潜在耐受性

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A mutant line of Arabidopsis thaliana that lacks a vacuolar membrane Zn2+/H+ antiporter MTP1 is sensitive to zinc. We examined the physiological changes in this loss-of-function mutant under high-Zn conditions to gain an understanding of the mechanism of adaptation to Zn stress. When grown in excessive Zn and observed using energy-dispersive X-ray analysis, wild-type roots were found to accumulate Zn in vacuolar-like organelles but mutant roots did not. The Zn content of mutant roots, determined by chemical analysis, was one-third that of wild-type roots grown in high-Zn medium. Severe inhibition of root growth was observed in mtp1-1 seedlings in 500 μM ZnSO4. Suppression of cell division and elonga-tion by excessive Zn was reversible and the cells resumed growth in normal medium. In mutant roots, a marked formation of reactive oxygen species (ROS) appeared in the meristematic zone, where the MTP1 gene was highly expressed. Zn treatment enhanced the expression of several genes involved in Zn tolerance: namely, the plasma membrane Zn2+-export ATPase, HMA4, and plasma and vacuolar membrane proton pumps. CuZn-superoxide dismutases, involved in the detoxification of ROS, were also induced. The expression of plasma membrane Zn-uptake transporter, ZIP1, was suppressed. The up- or down-regulation of these genes might confer the resistance to Zn toxicity. These results indicate an essential role of MTP1 in detoxification of excessive Zn and provide novel information on the latent adaptation mechanism to Zn stress, which is hidden by MTP1.
机译:缺少液泡膜Zn 2 + / H + 逆向转运蛋白MTP1的拟南芥突变株对锌敏感。我们研究了在高锌条件下该功能丧失突变体的生理变化,以了解对锌胁迫适应的机制。当生长在过量的锌中并使用能量色散X射线分析观察时,发现野生型根在液泡状细胞器中积累锌,而突变根则没有。通过化学分析确定的突变根的锌含量是在高锌培养基中生长的野生型根的锌含量的三分之一。在500μMZnSO 4 中的mtp1-1幼苗中观察到严重的根系生长抑制作用。过量的锌抑制细胞分裂和伸长是可逆的,并且细胞在正常培养基中恢复生长。在突变根中,在分生区中明显形成了活性氧(ROS),MTP1基因在该处高度表达。锌处理增强了几个与锌耐性有关的基因的表达:即质膜Zn 2 + -出口ATPase,HMA4,质膜和液泡膜质子泵。还诱导了参与ROS解毒的CuZn超氧化物歧化酶。质膜锌吸收转运蛋白ZIP1的表达被抑制。这些基因的上调或下调可能赋予对锌毒性的抗性。这些结果表明,MTP1在过量锌的解毒中具有重要作用,并提供了有关MTP1隐藏的对锌胁迫潜在适应机制的新信息。

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