盐芥中3型金属硫蛋白基因TsMT3的克隆与特征分析。

Xian Q Quan, Zeng L Wang, Hui Zhang, Yu P Bi
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引用次数: 9

摘要

从盐菜(Thellungiella salsuginea) 200 mM NaCl胁迫芽中分离到全长3型植物金属硫蛋白cDNA。TsMT3 cDNA序列全长447 bp,开放阅读框(ORF)全长207 bp,编码69个残基肽,分子量为7.52 kDa。Southern blot分析表明,在salsuginet基因组中只有一个TsMT3拷贝。PEG6000、200 mM NaCl、50 microM ABA、4℃、40 microM CuSO(4)或25 microM CdCl2胁迫均能促进TsMT3 mRNA的积累。将表达载体pET28-TsMT3在大肠杆菌中进行异源表达,以确定TsMT3对重金属耐受的贡献。在2 mM CuSO4、0.3 mM Pb(NO3)2或0.4 mM CdCl2存在下,表达TsMT3的细胞表现出更强的金属耐受性,积累的金属比对照组多。我们认为TsMT3可能参与了金属稳态、耐受性和活性氧(ROS)清除的过程。
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Cloning and characterization of TsMT3, a type 3 metallothionein gene from salt cress (Thellungiella salsuginea).

A full-length type 3 plant metallothionein cDNA was isolated from 200 mM NaCl stressed shoots of the salt cress (Thellungiella salsuginea). The 447 bp TsMT3 cDNA sequence has a 207 bp open reading frame (ORF) and encodes a deduced 69 residue peptide of molecular weight 7.52 kDa. Southern blot analysis indicates that, there is only one copy of TsMT3 in the T. salsuginea genome. The accumulation of TsMT3 mRNA is enhanced by the stress imposed by PEG6000, 200 mM NaCl, 50 microM ABA, 4 degrees C, 40 microM CuSO(4) or 25 microM CdCl2. The expression vector pET28-TsMT3 was heterologously expressed in Escherichia coli to define the contribution of TsMT3 to heavy metal tolerance. In the presence of 2 mM CuSO4, 0.3 mM Pb(NO3)2 or 0.4 mM CdCl2, TsMT3 expressing cells exhibited enhanced metal tolerance and accumulated more metal than the controls. We believe that TsMT3 is probably involved in the processes of metal homeostasis, tolerance, and reactive oxygen species (ROS) scavenging.

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