Velázquez L, Camarena L, Reyes J L, Bastarrachea F
Departamento de Biología Molecular, Universidad Nacional Autónoma de México, D.F.
J Bacteriol. 1991 May;173(10):3261-4. doi: 10.1128/jb.173.10.3261-3264.1991.
Individual mutations which affected each of the two Shine-Dalgarno sequences at the 5' untranslated region of the gltB gene of Escherichia coli were characterized. They were isolated in plasmids carrying a gltB'-'lacZ protein fusion preceded by the regulatory region of the gltBDF operon. Subcloning and nucleotide sequencing of approximately 1,206 bp of DNA encompassing the gltBDF regulatory region showed that the mutations affected the first base at each of the two identical Shine-Dalgarno sequences, SD1 and SD2, located 40 and 8 bases, respectively, upstream from the putative gltB open reading frame. Only mutation gltB2r227, an adenine in place of a guanine, affecting the first base of SD2, lowered beta-galactosidase expression significantly, i.e., about fivefold. The results suggest that SD2 is the preferred functional site at which ribosomes initiate gltB mRNA translation.
对影响大肠杆菌gltB基因5'非翻译区两个Shine-Dalgarno序列的单个突变进行了表征。它们是在携带gltB'-'lacZ蛋白融合体的质粒中分离得到的,该融合体之前是gltBDF操纵子的调控区。对包含gltBDF调控区的约1206 bp DNA进行亚克隆和核苷酸测序表明,这些突变影响了两个相同的Shine-Dalgarno序列SD1和SD2中每个序列的第一个碱基,它们分别位于假定的gltB开放阅读框上游40和8个碱基处。只有突变gltB2r227(腺嘌呤取代鸟嘌呤)影响SD2的第一个碱基,显著降低了β-半乳糖苷酶的表达,即约五倍。结果表明,SD2是核糖体启动gltB mRNA翻译的首选功能位点。