Brosius J, Walz A
Gene. 1982 Feb;17(2):223-8. doi: 10.1016/0378-1119(82)90076-2.
The insertion of an Escherichia coli IS2 element upstream from a cloned yeast TRP5 gene results in an increased level of active tryptophan synthase in trpAB E. coli host cells. This insertion occurs about 60 bp upstream from the first AUG of the TRP5 gene and is associated with a duplication of the sequence TTACA at the target site. The nucleotide sequence corresponding to the first 173 amino acids of the yeast TRP5 gene has also been determined. The N-terminal region of the yeast tryptophan synthase includes areas of strong homology with the alpha-subunit of the corresponding E. coli enzyme. Sequences from the 5' untranslated region upstream from the TRP5 gene are compared to homologous areas of other yeast genes.
在克隆的酵母TRP5基因上游插入一个大肠杆菌IS2元件,会导致trpAB大肠杆菌宿主细胞中活性色氨酸合酶水平升高。这种插入发生在TRP5基因第一个AUG上游约60 bp处,并与靶位点处的TTACA序列重复有关。还确定了酵母TRP5基因前173个氨基酸对应的核苷酸序列。酵母色氨酸合酶的N端区域与相应大肠杆菌酶的α亚基有很强的同源性区域。将TRP5基因上游5'非翻译区的序列与其他酵母基因的同源区域进行比较。