生物
亚克隆
操纵子
闪耀达尔加诺序列
核糖体结合位点
五素未翻译区
遗传学
紫胶操纵子
起始密码子
打开阅读框
真核翻译
大肠杆菌
基因
分子生物学
质粒
碱基对
上游开放阅读框
非翻译区
翻译(生物学)
信使核糖核酸
肽序列
作者
Laura Evelia Torres Velázquez,Laura Camarena,José Luis Reyes,Fernando Bastarrachea
标识
DOI:10.1128/jb.173.10.3261-3264.1991
摘要
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.
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