Watanabe I, Serizawa N
Biomedical Research Laboratories, Sankyo Co. Ltd, 1-2-58, Hiromachi, Shinagawa-ku, Tokyo 140, Japan.
Gene. 1998 Mar 27;210(1):109-16. doi: 10.1016/s0378-1119(98)00041-9.
We have characterized the transcriptional regulation of ML-236B.Na and phenobarbital-inducible cytochrome P450sca-2 (CytP450sca-2) from Streptomyces carbophilus, an industrial pravastatin-producing strain. ML-236B.Na and phenobarbital enhanced the expression of the cytP450sca-2 gene in S. carbophilus. The cytP450sca-2 gene was also ML-236B.Na-inductive in S. lividans. Analysis of various deletion and mutation of the 5'-flanking region of the cytP450sca-2 gene revealed that the 1-kb region was required for ML-236B.Na-dependent CytP450sca-2 induction. We have found a putative ORF in the 5'-flanking region that encodes a protein of 174 amino acid residues containing a helix-turn-helix DNA-binding motif. A gel mobility shift assay showed that the protein was bound by an imperfect palindromic sequence between -46bp and -24bp in the 5'-flanking region, and ML-236B.Na was found to inhibit its binding. These findings suggest that induction of cytP450sca-2 is negatively regulated at the transcriptional level and that the protein encoded by the putative ORF is possibly functional as a repressor of the cytP450sca-2 gene.
我们已经对来自嗜碳链霉菌(一种生产普伐他汀的工业菌株)的ML-236B.Na和苯巴比妥诱导型细胞色素P450sca-2(CytP450sca-2)的转录调控进行了表征。ML-236B.Na和苯巴比妥增强了嗜碳链霉菌中cytP450sca-2基因的表达。cytP450sca-2基因在变铅青链霉菌中对ML-236B.Na也有诱导作用。对cytP450sca-2基因5'侧翼区的各种缺失和突变分析表明,1 kb区域是ML-236B.Na依赖的CytP450sca-2诱导所必需的。我们在5'侧翼区发现了一个推定的开放阅读框,它编码一个含有螺旋-转角-螺旋DNA结合基序的174个氨基酸残基的蛋白质。凝胶迁移率变动分析表明,该蛋白质与5'侧翼区-46bp至-24bp之间的一个不完全回文序列结合,并且发现ML-236B.Na抑制其结合。这些发现表明,cytP450sca-2的诱导在转录水平上受到负调控,并且推定的开放阅读框编码的蛋白质可能作为cytP450sca-2基因的阻遏物发挥作用。