Teo I, Sedgwick B, Demple B, Li B, Lindahl T
EMBO J. 1984 Sep;3(9):2151-7. doi: 10.1002/j.1460-2075.1984.tb02105.x.
The expression of several inducible enzymes for repair of alkylated DNA in Escherichia coli is controlled by the ada+ gene. This regulatory gene has been cloned into a multicopy plasmid and shown to code for a 37-kd protein. Antibodies raised against homogeneous O6-methylguanine-DNA methyltransferase (the main repair activity for mutagenic damage in alkylated DNA) were found to cross-react with this 37-kd protein. Cell extracts from several independently derived ada mutants contain variable amounts of an altered 37-kd protein after an inducing alkylation treatment. In addition, an 18-kd protein identical with the previously isolated O6-methyl-guanine-DNA methyltransferase has been identified as a product of the ada+ gene. The smaller polypeptide is derived from the 37-kd protein by proteolytic processing.
大肠杆菌中几种用于修复烷基化DNA的诱导酶的表达受ada⁺基因控制。这个调控基因已被克隆到多拷贝质粒中,并被证明编码一种37千道尔顿的蛋白质。针对同源O6-甲基鸟嘌呤-DNA甲基转移酶(烷基化DNA中诱变损伤的主要修复活性)产生的抗体被发现与这种37千道尔顿的蛋白质发生交叉反应。经过诱导性烷基化处理后,来自几个独立衍生的ada突变体的细胞提取物含有不同量的一种改变的37千道尔顿蛋白质。此外,一种与先前分离的O6-甲基鸟嘌呤-DNA甲基转移酶相同的18千道尔顿蛋白质已被鉴定为ada⁺基因的产物。较小的多肽是通过蛋白水解加工从37千道尔顿的蛋白质衍生而来的。