Kreidberg J A, Kelly T J
Mol Cell Biol. 1986 Aug;6(8):2903-9. doi: 10.1128/mcb.6.8.2903-2909.1986.
The promoter of the human thymidine kinase gene was defined by DNA sequence and genetic analyses. Mutant plasmids with deletions extending into the promoter region from both the 5' and 3' directions were constructed. The mutants were tested in a gene transfer system for the ability to transform TK- cells to the TK+ phenotype. This analysis delimited the functional promoter to within an 83-base-pair region upstream of the mRNA cap site. This region contains sequences common to other eucaryotic promoters including G X C-rich hexanucleotides, a CAAT box, and an A X T-rich region. The CAAT box is in an inverted orientation and is part of a 9-base-pair sequence repeated twice in the promoter region. Comparison of the genomic sequence with the cDNA sequence defined the first exon of the thymidine kinase gene.
通过DNA序列和遗传分析确定了人胸苷激酶基因的启动子。构建了从5'和3'两个方向延伸到启动子区域的缺失突变质粒。在基因转移系统中测试这些突变体将TK-细胞转化为TK+表型的能力。该分析将功能性启动子限定在mRNA帽位点上游83个碱基对的区域内。该区域包含其他真核生物启动子共有的序列,包括富含GXC的六核苷酸、一个CAAT盒和一个富含AXT的区域。CAAT盒呈反向排列,是在启动子区域重复两次的9个碱基对序列的一部分。基因组序列与cDNA序列的比较确定了胸苷激酶基因的第一个外显子。