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克隆终止抑制因子的特定集合:同基因UAG、UAA和UGA抑制性tRNA的体内活性

Defined set of cloned termination suppressors: in vivo activity of isogenetic UAG, UAA, and UGA suppressor tRNAs.

作者信息

Raftery L A, Egan J B, Cline S W, Yarus M

出版信息

J Bacteriol. 1984 Jun;158(3):849-59. doi: 10.1128/jb.158.3.849-859.1984.

Abstract

We have cloned an isogenetic set of UAG, UAA, and UGA suppressors. These include the Su7 -UAG, Su7 -UAA, and Su7 -UGA suppressors derived from base substitutions in the anticodon of Escherichia coli tRNATrp and also Su9 , a UGA suppressor derived from a base substitution in the D-arm of the same tRNA. These genes are cloned on high-copy-number plasmids under lac promoter control. The construction of the Su7 -UAG plasmid and the wild-type trpT plasmid have been previously described ( Yarus , et al., Proc. Natl. Acad. Sci. U.S.A. 77:5092-5097, 1980). Su7 -UAA ( trpT177 ) is a weak suppressor which recognizes both UAA and UAG nonsense codons and probably inserts glutamine. Su7 -UGA ( trpT176 ) is a strong UGA suppressor which may insert tryptophan. Su9 ( trpT178 ) is a moderately strong UGA suppressor which also recognizes UGG (Trp) codons, and it inserts tryptophan. The construction of these plasmids is detailed within. Data on the DNA sequences of these trpT alleles and on amino acid specificity of the suppressors are presented. The efficiency of the cloned suppressors at certain nonsense mutations has been measured and is discussed with respect to the context of these codons.

摘要

我们克隆了一组同基因的UAG、UAA和UGA抑制基因。其中包括源自大肠杆菌tRNATrp反密码子碱基替换的Su7 -UAG、Su7 -UAA和Su7 -UGA抑制基因,以及源自同一tRNA D臂碱基替换的UGA抑制基因Su9。这些基因被克隆到在乳糖启动子控制下的高拷贝数质粒上。Su7 -UAG质粒和野生型trpT质粒的构建先前已有描述(亚鲁斯等人,《美国国家科学院院刊》77:5092 - 5097,1980年)。Su7 -UAA(trpT177)是一种弱抑制基因,可识别UAA和UAG无义密码子,可能插入谷氨酰胺。Su7 -UGA(trpT176)是一种强UGA抑制基因,可能插入色氨酸。Su9(trpT178)是一种中等强度的UGA抑制基因,也可识别UGG(Trp)密码子,并插入色氨酸。这些质粒的构建细节如下。文中给出了这些trpT等位基因DNA序列以及抑制基因氨基酸特异性的数据。已测定了克隆的抑制基因在某些无义突变处的效率,并结合这些密码子的上下文进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/215519/88ca035ba550/jbacter00235-0093-a.jpg

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