CHARACTERIZATION OF O6-METHYLGUANINE-DNA METHYLTRANSFERASE IN TRANSGENIC MICE INTRODUCED WITH THE ESCHERICHIA-COLI ADA GENE

被引:19
作者
NAKATSURU, Y
MATSUKUMA, S
SEKIGUCHI, M
ISHIKAWA, T
机构
[1] UNIV TOKYO,FAC MED,DEPT PATHOL,7-3-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
[2] JAPANESE FDN CANC RES,INST CANC,DEPT EXPTL PATHOL,TOKYO 170,JAPAN
[3] JAPANESE FDN CANC RES,INST CANC,DEPT CELL BIOL,TOKYO 170,JAPAN
[4] KYUSHU UNIV,FAC MED,DEPT BIOCHEM,FUKUOKA 812,JAPAN
来源
MUTATION RESEARCH | 1991年 / 254卷 / 03期
关键词
O6-METHYLGUANINE-DNA METHYLTRANSFERASE; TRANSGENIC MOUSE; ENZYME INDUCTION; METHYLNITROSOUREA RESISTANCE;
D O I
10.1016/0921-8777(91)90060-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The characteristics of O6-methylguanine-DNA methyltransferase (O6-MTase) produced in transgenic mice, in which the introduced E. coli ada gene was expressed under the control of the metallothionein promoter, were investigated. Liver extracts from transgenic homozygotes showed approximately 3 times the control activity, a marked increase of up to about 8 times the non-transgenic control levels being observed 10 h after zinc treatment. Examination of the substrate specificity of the enzyme revealed that the activity in the transgenic mice is due to the introduced foreign gene. The enzyme possessed methylphosphotriester-DNA methyltransferase as well as O6-MTase, characteristic of the E. coli Ada protein. Comparison of differences in biological response between transgenic and non-transgenic mice after treatment with the alkylating carcinogen methylnitrosourea (MNU) at various doses revealed transgenic mice to be more capable of repairing O6-MTase activity, only showing signs of exhaustion at very high levels of exposure. In non-transgenic mice, on the other hand, the basal level of O6-MTase was low, and the activity was hardly detectable when the animals were treated with MNU.
引用
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页码:225 / 230
页数:6
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