Role of ornithine decarboxylase antizyme inhibitor in vivo

被引:32
作者
Tang, Hua [1 ,2 ]
Ariki, Kimi [1 ]
Ohkido, Makiko [3 ]
Murakami, Yasuko [3 ,4 ]
Matsufuji, Senya [3 ]
Li, Zhenghua [1 ]
Yamamura, Ken-ichi [1 ]
机构
[1] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Dev Genet, Kumamoto 8600811, Japan
[2] Chongqing Med Univ, Minist Educ, Key Lab Mol Infect Dis, Chongqing 400016, Peoples R China
[3] Jikei Univ, Sch Med, Dept Mol Biol, Tokyo 1058461, Japan
[4] Musashino Univ, Pharmaceut Sci Res Inst, Fac Pharm, Tokyo 2028585, Japan
关键词
POLYAMINE METABOLISM; RAT-LIVER; CELL-PROLIFERATION; MESSENGER-RNA; GENE; GROWTH; MICE; TRANSFORMATION; OVEREXPRESSION; CARCINOGENESIS;
D O I
10.1111/j.1365-2443.2008.01249.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ornithine decarboxylase (ODC) antizyme inhibitor (AZI) has been shown to regulate ODC activity in cell cultures. However, its biological functions in an organism remain unknown. An embryonic stem (ES) cell clone was established, in which the Azin1 gene was disrupted by the gene trap technique. To identify the function of Azin1 gene in vivo, a mutant mouse line was generated using these trapped ES cells. Homozygous mutant mice died at P0 with abnormal liver morphology. Further analysis indicated that the deletion of Azin1 in homozygous mice resulted in the degradation of ODC, and reduced the biosynthesis of putrescine and spermidine. Our results thus show that AZI plays an important role in regulating the levels of ODC, putrescine and spermidine in mice, and is essential for the survival of mice.
引用
收藏
页码:79 / 87
页数:9
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