Stuart G W, Searle P F, Chen H Y, Brinster R L, Palmiter R D
Proc Natl Acad Sci U S A. 1984 Dec;81(23):7318-22. doi: 10.1073/pnas.81.23.7318.
To define DNA sequences involved in mouse metallothionein-I (MT-I) gene promoter function and metal regulation, we fused the 5' flanking sequences of the MT-I gene to the coding sequences of a viral thymidine kinase (TK) gene. A series of 5' deletion, 3' deletion, linker-scanning, and internal deletion mutants of the MT-I promoter was constructed and assayed by microinjection into mouse eggs. The results indicate that at least two related promoter elements can confer some metal regulation independently. Those mutations that had the most severe effect on regulation impinge on a 12-base-pair conserved sequence that is repeated several times within the mouse MT-I and other MT promoters. To test the regulatory function of this sequence, it was synthesized as a pair of complementary oligonucleotides and inserted into the promoter of the TK gene. A single insertion of this sequence conferred limited metal regulation onto the TK promoter, whereas a construct with two separate inserts was regulated as efficiently as the MT-I promoter.
为了确定参与小鼠金属硫蛋白-I(MT-I)基因启动子功能和金属调控的DNA序列,我们将MT-I基因的5'侧翼序列与病毒胸苷激酶(TK)基因的编码序列融合。构建了一系列MT-I启动子的5'缺失、3'缺失、接头扫描和内部缺失突变体,并通过显微注射到小鼠卵中进行检测。结果表明,至少有两个相关的启动子元件可以独立赋予一定的金属调控能力。那些对调控影响最严重的突变影响了一个12碱基对的保守序列,该序列在小鼠MT-I和其他MT启动子中重复出现多次。为了测试该序列的调控功能,将其合成为一对互补寡核苷酸并插入到TK基因的启动子中。该序列的单次插入赋予了TK启动子有限的金属调控能力,而具有两个单独插入片段的构建体的调控效率与MT-I启动子相同。