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牛转基因在黑腹果蝇铜/锌超氧化物歧化酶缺失突变体中的表型拯救

Phenotypic rescue by a bovine transgene in a Cu/Zn superoxide dismutase-null mutant of Drosophila melanogaster.

作者信息

Reveillaud I, Phillips J, Duyf B, Hilliker A, Kongpachith A, Fleming J E

机构信息

Linus Pauling Institute of Science and Medicine, Palo Alto, California 94306.

出版信息

Mol Cell Biol. 1994 Feb;14(2):1302-7. doi: 10.1128/mcb.14.2.1302-1307.1994.

Abstract

Null mutants for Cu/Zn superoxide dismutase (CuZnSOD) in Drosophila melanogaster are male sterile, have a greatly reduced adult life span, and are hypersensitive to paraquat. We have introduced a synthetic bovine CuZnSOD transgene under the transcriptional control of the D. melanogaster 5C actin promoter into a CuZnSOD-null mutant of D. melanogaster. This was carried out by P-element-mediated transformation of the Drosophila-bovine CuZnSOD transgene into a CuZnSOD+ recipient strain followed by genetic crossing of the transgene into a strain carrying the CuZnSOD-null mutation, cSODn108. The resulting transformants express bovine CuZnSOD exclusively to about 30% of normal Drosophila CuZnSOD levels. Expression of the Drosophila-bovine CuZnSOD transgene in the CuZnSOD-null mutant rescues male fertility and resistance to paraquat to apparently normal levels. However, adult life span is restored to only 30% of normal, and resistance to hyperoxia is 90% of that found in control flies. This striking differential restoration of pleiotropic phenotypes could be the result of a threshhold of CuZnSOD expression necessary for normal male fertility and resistance to the toxicity of paraquat or hyperoxia which is lower than the threshold required to sustain a normal adult life span. Alternatively, the differential rescue of fertility, resistance to active oxygen, and life span might indicate different cell-specific transcriptional requirements for these functions which are normally provided by the control elements of the native CuZnSOD gene but are only partly compensated for by the transcriptional control elements of the actin 5C promoter.

摘要

果蝇中铜锌超氧化物歧化酶(CuZnSOD)的无效突变体雄性不育,成虫寿命大幅缩短,对百草枯高度敏感。我们已将一个在黑腹果蝇5C肌动蛋白启动子转录控制下的合成牛CuZnSOD转基因导入黑腹果蝇的CuZnSOD无效突变体中。这是通过P因子介导将果蝇 - 牛CuZnSOD转基因转化到一个CuZnSOD +受体菌株中,然后通过基因杂交将该转基因导入携带CuZnSOD无效突变cSODn108的菌株中实现的。所得转化体仅表达牛CuZnSOD,其水平约为正常果蝇CuZnSOD水平的30%。在CuZnSOD无效突变体中表达果蝇 - 牛CuZnSOD转基因可将雄性生育力和对百草枯的抗性恢复到明显正常的水平。然而,成虫寿命仅恢复到正常水平的30%,对高氧的抗性为对照果蝇的90%。这种多效性表型的显著差异恢复可能是由于正常雄性生育力和对百草枯或高氧毒性的抗性所需的CuZnSOD表达阈值低于维持正常成虫寿命所需的阈值。或者,生育力、对活性氧的抗性和寿命的差异挽救可能表明这些功能对不同细胞特异性转录的需求,这些需求通常由天然CuZnSOD基因的控制元件提供,但仅部分地由肌动蛋白5C启动子的转录控制元件补偿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc97/358485/07cdeca3b841/molcellb00002-0446-a.jpg

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