University of Warsaw, Institute of Experimental Plant Biology, Warszawa, Poland.
Plant Biotechnol J. 2011 Jan;9(1):64-74. doi: 10.1111/j.1467-7652.2010.00531.x.
Genetic modification of Zn/Cd accumulation in roots and shoots for biofortification or phytoremediation is a focus of this manuscript. We expressed AtHMA4 (a P(₁B) ATPase involved in Zn and Cd transport), AtHMA4-trunc (lacking the C-terminal region) and AtHMA4-C terminus (the C-terminal region alone) in tobacco under the CaMV 35S constitutive promoter and examined accumulation and tolerance to both metals. Expression of AtHMA4 enhanced Zn translocation to the shoots only at 10 μM Zn but not at 0.5, 100 and 200 μM Zn. AtHMA4-trunc did not show this effect and instead reduced Zn translocation to the shoot. AtHMA4-expressing plants showed a decrease in cadmium uptake when exposed to 0.25 and 5 μM Cd; this was also observed with AtHMA4-trunc-expressing lines, although to a lesser extent. Expression of AtHMA4-C-terminus containing potential metal binding sites increased cadmium and zinc concentrations in roots and shoots up to fourfold. We have demonstrated that both AtHMA4 and AtHMA4 C-terminus could be candidate genes/sequences for engineering modifications of zinc and cadmium root/shoot partitioning. However, the phenotype of transformants depended on the external metal concentration, thus it might be difficult to engineer a plant displaying the desired metal-related phenotype when grown under varying conditions of metal supply.
该手稿的重点是对根和茎中的 Zn/Cd 积累进行遗传修饰,以进行生物强化或植物修复。我们在烟草中表达了 AtHMA4(一种参与 Zn 和 Cd 转运的 P(₁B)ATP 酶)、AtHMA4-trunc(缺失 C 端区域)和 AtHMA4-C 端(仅 C 端区域),并在 CaMV 35S 组成型启动子的控制下进行了研究,考察了它们对两种金属的积累和耐受性。AtHMA4 的表达仅在 10 μM Zn 时增强了 Zn 向地上部分的转运,但在 0.5、100 和 200 μM Zn 时则没有。AtHMA4-trunc 则没有这种作用,反而减少了 Zn 向地上部分的转运。在暴露于 0.25 和 5 μM Cd 时,表达 AtHMA4 的植株减少了镉的吸收;这也在表达 AtHMA4-trunc 的株系中观察到,尽管程度较轻。表达含有潜在金属结合位点的 AtHMA4 C 端使根和地上部分的镉和锌浓度增加了 4 倍。我们已经证明,AtHMA4 和 AtHMA4 C 端都可以作为工程改造 Zn 和 Cd 根/茎分配的候选基因/序列。然而,转化体的表型取决于外部金属浓度,因此,当在不同的金属供应条件下生长时,可能难以设计出显示所需金属相关表型的植物。