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异常表达人类鸟氨酸脱羧酶基因的转基因小鼠。

Transgenic mice aberrantly expressing human ornithine decarboxylase gene.

作者信息

Halmekytö M, Hyttinen J M, Sinervirta R, Utriainen M, Myöhänen S, Voipio H M, Wahlfors J, Syrjänen S, Syrjänen K, Alhonen L

机构信息

Department of Biochemistry & Biotechnology, University of Kuopio, Finland.

出版信息

J Biol Chem. 1991 Oct 15;266(29):19746-51.

PMID:1717470
Abstract

We have generated transgenic mice carrying human ornithine decarboxylase gene. Two different transgene constructs were used: (i) a 5'-truncated human ornithine decarboxylase gene and (ii) an intact human ornithine decarboxylase gene. Transgenic mice carrying the 5'-truncated gene did not express human ornithine decarboxylase-specific mRNA. Transgenic mice carrying the intact human ornithine decarboxylase gene expressed human-specific ornithine decarboxylase mRNA in all tissues studied. However, as indicated by actual enzyme assays, the expression pattern was highly unusual. In comparison with their wild-type littermates, the transgenic mice exhibited greatly elevated enzyme activity in almost every tissue studied. Ornithine decarboxylase activity was moderately elevated in parenchymal organs such as liver, kidney, and spleen. Tissues like heart, muscle, lung, thymus, testis, and brain displayed an enzyme activity that was 20 to 80 times higher than that in the respective tissues of nontransgenic animals. The offspring of the first transgenic male founder animal did not show any overt abnormalities, yet their reproductive performance was reduced. The second transgenic founder animal, showing similar aberrant expression of ornithine decarboxylase in all tissues studied, including an extremely high activity in testis, was found to be infertile. Histological examination of the tissues of the latter animal revealed marked changes in testicular morphology. The germinal epithelium was hypoplastic, and the spermatogenesis was virtually totally shut off. Similar examination of male members of the first transgenic mouse line revealed comparable, yet less severe, histological changes in testis.

摘要

我们培育出了携带人类鸟氨酸脱羧酶基因的转基因小鼠。使用了两种不同的转基因构建体:(i)一个5'端截短的人类鸟氨酸脱羧酶基因和(ii)一个完整的人类鸟氨酸脱羧酶基因。携带5'端截短基因的转基因小鼠不表达人类鸟氨酸脱羧酶特异性mRNA。携带完整人类鸟氨酸脱羧酶基因的转基因小鼠在所有研究的组织中都表达人类特异性鸟氨酸脱羧酶mRNA。然而,如实际酶活性测定所示,其表达模式非常异常。与它们的野生型同窝小鼠相比,转基因小鼠在几乎所有研究的组织中都表现出酶活性大幅升高。在肝脏、肾脏和脾脏等实质器官中,鸟氨酸脱羧酶活性适度升高。心脏、肌肉、肺、胸腺、睾丸和大脑等组织的酶活性比非转基因动物相应组织中的酶活性高20至80倍。第一代转基因雄性奠基动物的后代没有表现出任何明显异常,但其繁殖性能有所下降。第二代转基因奠基动物在所有研究的组织中都表现出类似的鸟氨酸脱羧酶异常表达,包括睾丸中的活性极高,结果发现其不育。对后一种动物的组织进行组织学检查发现睾丸形态有明显变化。生精上皮发育不全,精子发生几乎完全停止。对第一代转基因小鼠品系的雄性成员进行类似检查发现睾丸有类似但不太严重的组织学变化。

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