Ishida Masami, Oshima Tairo
Laboratory of Marine Biochemistry, Tokyo University of Fisheries, 4-5-7 Konan, Minato-ku, Tokyo 108-8477, Japan.
J Biochem. 2002 Jul;132(1):63-70. doi: 10.1093/oxfordjournals.jbchem.a003199.
To overexpress broad kinds of GC-rich genes in Escherichia coli, we examined how the structures of leader open reading frames (leader ORFs) affect the expression of GC-rich genes, such as polA, trpA, and trpB, from Thermus thermophilus. When a leader ORF overlapped with the polA-initiation codon by 1 bp in the TGATG motif, gene expression increased by more than 3-fold compared to when a leader ORF was several-bp distant from the initiation codon. A 4-bp overlap with the ATGA motif was more effective than a 1-bp overlap with the TGATG motif. When a 4-bp overlapping leader ORF was placed in front of the successive trpB and trpA genes, the trpA gene was poorly expressed whereas the trpB gene was overexpressed. Mutation analysis revealed that the expression of the trpA gene was strongly enhanced by replacing G and C in the translation termination region of the leader ORF with A and T. In contrast, other mutations, such as alterations between synonymous codons in the trpA-coding region, produced diminished gene expression. Using the most effective leader ORF obtained from these results, new expression vectors were constructed.
为了在大肠杆菌中过表达多种富含GC的基因,我们研究了前导开放阅读框(前导ORF)的结构如何影响嗜热栖热菌中富含GC的基因(如polA、trpA和trpB)的表达。当前导ORF在TGATG基序中与polA起始密码子重叠1个碱基对时,与前导ORF与起始密码子相距几个碱基对时相比,基因表达增加了3倍以上。与TGATG基序重叠1个碱基对相比,与ATGA基序重叠4个碱基对更有效。当一个4碱基对重叠的前导ORF置于连续的trpB和trpA基因之前时,trpA基因表达不佳,而trpB基因过表达。突变分析表明,通过将前导ORF翻译终止区域中的G和C替换为A和T,trpA基因的表达得到了强烈增强。相比之下,其他突变,如trpA编码区域中同义密码子之间的改变,导致基因表达降低。利用这些结果获得的最有效的前导ORF,构建了新的表达载体。